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<div class="pre-content"><div><div class="bk_prnt"><p class="small">NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.</p><p>PDQ Cancer Information Summaries [Internet]. Bethesda (MD): National Cancer Institute (US); 2002-. </p></div><div class="iconblock clearfix whole_rhythm no_top_margin bk_noprnt"><a class="img_link icnblk_img" title="Table of Contents Page" href="/books/n/pdqcis/"><img class="source-thumb" src="/corehtml/pmc/pmcgifs/bookshelf/thumbs/th-pdqcis-lrg.png" alt="Cover of PDQ Cancer Information Summaries" height="100px" width="80px" /></a><div class="icnblk_cntnt eight_col"><h2>PDQ Cancer Information Summaries [Internet].</h2><a data-jig="ncbitoggler" href="#__NBK65842_dtls__">Show details</a><div style="display:none" class="ui-widget" id="__NBK65842_dtls__"><div>Bethesda (MD): <a href="http://www.cancer.gov/" ref="pagearea=page-banner&targetsite=external&targetcat=link&targettype=publisher">National Cancer Institute (US)</a>; 2002-.</div></div><div class="half_rhythm"></div><div class="bk_noprnt"><form method="get" action="/books/n/pdqcis/" id="bk_srch"><div class="bk_search"><label for="bk_term" class="offscreen_noflow">Search term</label><input type="text" title="Search this book" id="bk_term" name="term" value="" data-jig="ncbiclearbutton" /> <input type="submit" class="jig-ncbibutton" value="Search this book" submit="false" style="padding: 0.1em 0.4em;" /></div></form></div></div></div></div></div>
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<div class="main-content lit-style" itemscope="itemscope" itemtype="http://schema.org/CreativeWork"><div class="meta-content fm-sec"><h1 id="_NBK65842_"><span class="title" itemprop="name">Wilms Tumor and Other Childhood Kidney Tumors Treatment (PDQ®)</span></h1><div class="subtitle whole_rhythm">Health Professional Version</div><p class="contrib-group"><span itemprop="author">PDQ Pediatric Treatment Editorial Board</span>.</p><p class="small">Published online: November 5, 2020.</p></div><div class="jig-ncbiinpagenav body-content whole_rhythm" data-jigconfig="allHeadingLevels: ['h2'],smoothScroll: false" itemprop="text"><div id="_abs_rndgid_" itemprop="description"><p id="CDR0000062789__1189">This PDQ cancer information summary for health professionals provides comprehensive, peer-reviewed, evidence-based information about the treatment of Wilms tumor and other childhood kidney tumors. It is intended as a resource to inform and assist clinicians who care for cancer patients. It does not provide formal guidelines or recommendations for making health care decisions.</p><p id="CDR0000062789__1190">This summary is reviewed regularly and updated as necessary by the PDQ Pediatric Treatment Editorial Board, which is editorially independent of the National Cancer Institute (NCI). The summary reflects an independent review of the literature and does not represent a policy statement of NCI or the National Institutes of Health (NIH).</p></div><div id="CDR0000062789__755"><h2 id="_CDR0000062789__755_">General Information About Childhood Kidney Tumors</h2><p id="CDR0000062789__758">Dramatic improvements in survival have been achieved for children and adolescents with cancer. Between 1975 and 2010, childhood cancer mortality decreased by more than 50%.[<a class="bk_pop" href="#CDR0000062789_rl_755_1">1</a>] For children younger than 15 years with Wilms tumor, the 5-year survival rate has increased over the same time from 74% to 88%.[<a class="bk_pop" href="#CDR0000062789_rl_755_1">1</a>] Childhood and adolescent cancer survivors require close monitoring because cancer therapy side effects may persist or develop months or years after treatment. (Refer to the PDQ summary on <a href="/books/n/pdqcis/CDR0000343584/"> Late Effects of Treatment for Childhood Cancer</a> for specific information about the incidence, type, and monitoring of late effects in childhood and adolescent cancer survivors.)</p><p id="CDR0000062789__759">Childhood kidney cancers account for about 7% of all childhood cancers. Most childhood kidney cancers are Wilms tumor, but in the 15- to 19-year age group, most tumors are renal cell carcinoma. Wilms tumor can affect one kidney (unilateral) or both kidneys (bilateral). Less common types of childhood kidney tumors include <a href="#CDR0000062789__17">rhabdoid tumors</a>, <a href="#CDR0000062789__10">clear cell sarcoma</a>, <a href="#CDR0000062789__429">congenital mesoblastic nephroma</a>, <a href="#CDR0000062789__20">Ewing sarcoma of the kidney</a>, <a href="#CDR0000062789__1241">primary renal myoepithelial carcinoma</a>, <a href="#CDR0000062789__150">cystic partially differentiated nephroblastoma</a>, <a href="#CDR0000062789__383">multilocular cystic nephroma</a>,<a href="#CDR0000062789__438"> primary renal synovial sarcoma</a>, and <a href="#CDR0000062789__440">anaplastic sarcoma</a>. <a href="#CDR0000062789__436">Nephroblastomatosis</a> of the kidney is a type of nonmalignant neoplasia.[<a class="bk_pop" href="#CDR0000062789_rl_755_2">2</a>,<a class="bk_pop" href="#CDR0000062789_rl_755_3">3</a>]</p><div id="CDR0000062789_rl_755"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_755_1">Smith MA, Altekruse SF, Adamson PC, et al.: Declining childhood and adolescent cancer mortality. Cancer 120 (16): 2497-506, 2014.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_755_2">Ahmed HU, Arya M, Levitt G, et al.: Part I: Primary malignant non-Wilms' renal tumours in children. Lancet Oncol 8 (8): 730-7, 2007.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_755_3">Ahmed HU, Arya M, Levitt G, et al.: Part II: Treatment of primary malignant non-Wilms' renal tumours in children. Lancet Oncol 8 (9): 842-8, 2007.</div></li></ol></div></div><div id="CDR0000062789__1"><h2 id="_CDR0000062789__1_">Wilms Tumor</h2><div id="CDR0000062789__723"><h3>Incidence of Wilms Tumor</h3><p id="CDR0000062789__724">Wilms tumor is the most frequent tumor of the kidney in infants and children. The incidence of Wilms tumor is 8.2 cases for every 1 million children younger than 15 years, or one case per 10,000 infants.[<a class="bk_pop" href="#CDR0000062789_rl_1_1">1</a>] Approximately 650 cases of Wilms tumor are diagnosed in the United States each year. The incidence is substantially lower in Asians.[<a class="bk_pop" href="#CDR0000062789_rl_1_1">1</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_2">2</a>] </p><p id="CDR0000062789__1254">The male to female ratio in unilateral cases of Wilms tumor is 0.92 to 1.00, but in bilateral cases, it is 0.60 to 1.00. The mean age at diagnosis is 44 months in unilateral cases and 31 months in bilateral cases of Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_3">3</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_4">4</a>] About 10% of children with Wilms tumor have an associated congenital malformation syndrome.[<a class="bk_pop" href="#CDR0000062789_rl_1_5">5</a>]</p></div><div id="CDR0000062789__1084"><h3>Syndromes and Other Conditions Associated With Wilms Tumor</h3><p id="CDR0000062789__1087">Wilms tumor typically develops in otherwise healthy children without any predisposition to developing cancer; however, approximately 10% of children with Wilms tumor have been reported to have a congenital anomaly.[<a class="bk_pop" href="#CDR0000062789_rl_1_5">5</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_6">6</a>] In patients with congenital anomalies and Wilms tumor, nephrogenic rests have been reported in 60% of cases.[<a class="bk_pop" href="#CDR0000062789_rl_1_7">7</a>] Of 295 consecutive patients with Wilms tumor seen at the Institut Curie in Paris, 52 (17.6%) had anomalies or syndromes, 43 of which were considered major, and 14 of which were genetically proven tumor predisposition syndromes.[<a class="bk_pop" href="#CDR0000062789_rl_1_8">8</a>] </p><p id="CDR0000062789__1255">Children with Wilms tumor may have associated hemihyperplasia and urinary tract anomalies, including cryptorchidism and hypospadias. Children may have recognizable phenotypic syndromes such as overgrowth, aniridia, genetic malformations, and others. These syndromes have provided clues to the genetic basis of the disease. The phenotypic syndromes and other conditions have been grouped into overgrowth and non-overgrowth categories (refer to <a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__1947/?report=objectonly" target="object" rid-figpopup="figCDR00000627891947" rid-ob="figobCDR00000627891947">Table 1</a>). Overgrowth syndromes and conditions are the result of excessive prenatal and postnatal somatic
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growth.[<a class="bk_pop" href="#CDR0000062789_rl_1_9">9</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_10">10</a>] </p><p id="CDR0000062789__1298">It is important to recognize that the absolute risk of Wilms tumor varies with the underlying condition or anomaly. For example, most patients with hemihyperplasia will not develop Wilms tumor. </p><div id="CDR0000062789__1947" class="table"><h3><span class="title">Table 1. Syndromes and Conditions Associated With Wilms Tumor<sup>a</sup></span></h3><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK65842.23/table/CDR0000062789__1947/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__CDR0000062789__1947_lrgtbl__"><table class="no_margin"><thead><tr><th colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Syndrome/Condition</th><th colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Gene</th><th colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Overgrowth Phenotype</th><th colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Non-Overgrowth Phenotype </th></tr><tr><th colspan="4" rowspan="1" style="text-align:center;vertical-align:top;">High Risk of Wilms Tumor (>20%)</th></tr></thead><tbody><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">WAGR syndrome</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>WT1</i> deletion</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Denys-Drash syndrome</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>WT1</i> missense mutation</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Perlman syndrome</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>DIS3L2</i> mutation</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Fanconi anemia with biallelic mutations in <i>BRCA2</i> (<i>FANCD1</i>) or <i>PALB2</i> (<i>FANCN</i>)</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>BRCA2</i>,
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<i>PALB2</i>
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</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Premature chromatid separation/mosaic variegated aneuploidy</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Biallelic <i>BUB1B</i> or <i>TRIP13</i> mutation</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td></tr><tr><td colspan="4" rowspan="1" style="text-align:center;vertical-align:top;"><b>Moderate Risk of Wilms Tumor (5%–20%)</b></td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Frasier syndrome</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>WT1</i> intron 9 splice mutation</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Beckwith-Wiedemann syndrome</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Uniparental disomy or H19 epimutation</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Simpson-Golabi-Behmel syndrome</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>GPC3</i> mutation</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td></tr><tr><td colspan="4" rowspan="1" style="text-align:center;vertical-align:top;"><b>Low Risk of Wilms Tumor (<5%)</b></td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Bloom syndrome</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Biallelic <i>BLM</i> mutation</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">DICER1 syndrome</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>DICER1</i> mutation</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Li-Fraumeni syndrome</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>TP53</i>,
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<i>CHEK2</i>
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</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Isolated hemihyperplasia</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Hyperparathyroidism-jaw tumor syndrome</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>CDC73</i> (also known as <i>HRPT2</i>) mutation</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">MULIBREY nanism syndrome</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>TRIM37</i> mutation</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>PIK3CA</i>-related segmental overgrowth including CLOVES syndrome</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>PIK3CA</i> mutation</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">9q22.3 microdeletion syndrome </td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">9q22.3</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Sotos syndrome</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>NSD1</i></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td></tr><tr><td colspan="1" rowspan="2" style="text-align:center;vertical-align:top;">Familial Wilms tumor</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>FWT1</i></td><td colspan="1" rowspan="2" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="2" style="text-align:center;vertical-align:top;">X</td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>FWT2</i></td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Genitourinary anomalies</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>WT1</i></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Sporadic aniridia</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"><i>WT1</i></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td></tr><tr><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">Trisomy 18</td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;"></td><td colspan="1" rowspan="1" style="text-align:center;vertical-align:top;">X</td></tr></tbody></table></div><div><div><dl class="temp-labeled-list small"><dt></dt><dd><div><p class="no_margin">CLOVES = congenital lipomatous overgrowth, vascular malformations, epidermal nevi, and skeletal/spinal abnormalities; MULIBREY = distinctive abnormalities of the (MU)scles, (LI)ver, (BR)ain, and (EY)es; WAGR = Wilms tumor, aniridia, genitourinary anomaly, and mental retardation.</p></div></dd><dt></dt><dd><div><p class="no_margin"><sup>a</sup>Adapted from Treger et al.[<a class="bk_pop" href="#CDR0000062789_rl_1_11">11</a>]</p></div></dd></dl></div></div></div><p id="CDR0000062789__1097">For information about the genes associated with Wilms tumor, including <i>WT1</i> and <i>WT2</i>, refer to the <a href="#CDR0000062789__1203">Genomics of Wilms Tumor</a> section of this summary.</p><div id="CDR0000062789__1086"><h4>Syndromic causes of Wilms tumor</h4><div id="CDR0000062789__2013"><h5><i>WT1</i>-related syndromes</h5><p id="CDR0000062789__1256"><i>WT1</i>-related syndromes include the following:</p><ul id="CDR0000062789__1257"><li class="half_rhythm"><div class="half_rhythm"><b>WAGR syndrome.</b> WAGR syndrome is characterized by the following: <dl id="CDR0000062789__1258" class="temp-labeled-list"><dt>-</dt><dd><p class="no_top_margin"><b>W</b>ilms tumor.</p></dd><dt>-</dt><dd><p class="no_top_margin"><b>A</b>niridia.</p></dd><dt>-</dt><dd><p class="no_top_margin"><b>G</b>enitourinary anomaly.</p></dd><dt>-</dt><dd><p class="no_top_margin">Mental <b>R</b>etardation. </p></dd></dl></div><div class="half_rhythm">The constellation of WAGR syndrome occurs in association with an interstitial deletion on chromosome 11 (del(11p13)) (prevalence is about 0.4% of children with Wilms tumor).[<a class="bk_pop" href="#CDR0000062789_rl_1_12">12</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_13">13</a>] The risk of Wilms tumor development in children with WAGR syndrome is approximately 50%; these children will present earlier and have a higher incidence of bilateral Wilms tumors (15%) than will children with nonsyndromic Wilms tumors.[<a class="bk_pop" href="#CDR0000062789_rl_1_14">14</a>] (Refer to the <a href="#CDR0000062789__1203">Genomics of Wilms Tumor</a> section of this summary for more information.)</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Denys-Drash syndrome and Frasier syndrome.</b> Genitourinary anomalies such as hypospadias, undescended testis, and others are associated with <i>WT1</i> mutations (prevalence is about 8%–10% of children with Wilms tumor). Children with XY genome with pseudo-hermaphroditism and/or renal disease (glomerulonephritis or nephrotic syndrome) who develop Wilms tumor may have Denys-Drash or Frasier syndrome (characterized by male hermaphroditism, primary amenorrhea, chronic renal failure, and other abnormalities),[<a class="bk_pop" href="#CDR0000062789_rl_1_15">15</a>] both of which are associated with mutations in the <i>WT1</i> gene.[<a class="bk_pop" href="#CDR0000062789_rl_1_16">16</a>] Specifically, germline missense mutations in the <i>WT1</i> gene are responsible for most cases of Wilms tumor that occur as part of Denys-Drash syndrome.[<a class="bk_pop" href="#CDR0000062789_rl_1_17">17</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_18">18</a>] The risk of Wilms tumor is about 90% for children with Denys-Drash syndrome, with bilateral disease developing in 20% of patients.[<a class="bk_pop" href="#CDR0000062789_rl_1_18">18</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_19">19</a>] In Frasier syndrome, splice-site <i>WT1</i> mutations result in an imbalance of <i>WT1</i> isoforms and a much lower incidence of Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_20">20</a>]</div></li></ul></div><div id="CDR0000062789__2014"><h5><i>WT2</i>-related syndromes</h5><p id="CDR0000062789__1260"><i>WT2</i>-related syndromes include the following:</p><ul id="CDR0000062789__1261"><li class="half_rhythm"><div><b>Beckwith-Wiedemann syndrome.</b> Beckwith-Wiedemann syndrome is an overgrowth syndrome characterized by asymmetric growth of one or more parts of the body, large tongue, omphalocele or umbilical hernia at birth, creases or pits in the skin near the ears, kidney abnormalities, and hypoglycemia (in neonates). It is also characterized by the development of Wilms tumor, rhabdomyosarcoma, and hepatoblastoma in the first decade of life. Approximately 15% of children with Beckwith-Wiedemann syndrome will have bilateral tumors.[<a class="bk_pop" href="#CDR0000062789_rl_1_21">21</a>]</div><div>Beckwith-Wiedemann syndrome is caused by altered expression of two gene clusters involved in growth control and cell-cycle progression regulated by two independent imprinting control regions (ICR1 [termed <i>telomeric ICR</i>] and ICR2 [termed <i>centromeric ICR</i>]) at chromosome 11p15.5. The two ICRs are characterized by differential methylation of maternal and paternal alleles. A variety of molecular mechanisms are implicated in Beckwith-Wiedemann syndrome pathogenesis, leading to unbalanced expression of imprinted genes within these two domains. Tumor predisposition results primarily from dysregulation at the telomeric domain of 11p15 (ICR1 gain of methylation [ICR1-GoM] and paternal uniparental disomy [UPD]) rather than at the centromeric domain of 11p15 (ICR2 loss of methylation [ICR2-LoM] and <i>CDKN1C</i> mutation).[<a class="bk_pop" href="#CDR0000062789_rl_1_22">22</a>] Approximately 15% of cases with clear-cut phenotypes have no molecular defects established so far.[<a class="bk_pop" href="#CDR0000062789_rl_1_23">23</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_24">24</a>]</div><div> The molecular subtypes of the syndrome predispose patients to the development of different tumor histotypes.[<a class="bk_pop" href="#CDR0000062789_rl_1_25">25</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_27">27</a>] </div><div>The prevalence of Beckwith-Wiedemann syndrome is about 1% of children with Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_21">21</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_28">28</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_30">30</a>] Approximately 10% of Beckwith-Wiedemann syndrome patients will develop Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_22">22</a>] Beckwith-Wiedemann syndrome patients with hemihyperplasia have a fourfold increased tumor risk over Beckwith-Wiedemann syndrome patients without hemihyperplasia.[<a class="bk_pop" href="#CDR0000062789_rl_1_31">31</a>] (Refer to the <a href="#CDR0000062789__1203">Genomics of Wilms Tumor</a> section of this summary for more information.)</div></li></ul></div><div id="CDR0000062789__2015"><h5>Other syndromic causes of Wilms tumor</h5><p id="CDR0000062789__1262">Other syndromic causes of Wilms tumor include the following:</p><ul id="CDR0000062789__1263"><li class="half_rhythm"><div class="half_rhythm"><b>Perlman syndrome.</b> Perlman syndrome—a rare, autosomal, recessively inherited, congenital overgrowth syndrome—is characterized by fetal gigantism, renal dysplasia and nephroblastomatosis, islet cell hypertrophy, multiple congenital anomalies, and mental retardation. Survivors have a high risk of developing Wilms tumor (75%).[<a class="bk_pop" href="#CDR0000062789_rl_1_32">32</a>] </div><div class="half_rhythm">Germline inactivating mutations in <i>DIS3L2</i> on chromosome 2q37 are associated with Perlman syndrome. Preliminary data suggest that <i>DIS3L2</i> plays a role in normal kidney development and in a subset of sporadic Wilms tumor cases.[<a class="bk_pop" href="#CDR0000062789_rl_1_33">33</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Simpson-Golabi-Behmel syndrome.</b> Simpson-Golabi-Behmel syndrome is characterized by macroglossia, macrosomia, renal and skeletal abnormalities, and increased risk of embryonal cancers.</div><div class="half_rhythm">The syndrome is caused by mutations or deletions in the <i>GPC3</i> and <i>GPC4</i> genes, and these genetic aberrations are believed to enhance the risk of Wilms tumor (8%).[<a class="bk_pop" href="#CDR0000062789_rl_1_34">34</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>CLOVES syndrome.</b> This syndrome is characterized by the following: <dl id="CDR0000062789__1865" class="temp-labeled-list"><dt>-</dt><dd><p class="no_top_margin"><b>C</b>ongenital <b>L</b>ipomatous <b>O</b>vergrowth.</p></dd><dt>-</dt><dd><p class="no_top_margin"><b>V</b>ascular malformations.</p></dd><dt>-</dt><dd><p class="no_top_margin"><b>E</b>pidermal nevi.</p></dd><dt>-</dt><dd><p class="no_top_margin"><b>S</b>keletal/spinal abnormalities. </p></dd></dl></div><div class="half_rhythm">This syndrome results from postzygotic, somatic mutations in <i>PIK3CA</i>, which may involve large or small regions of the child.[<a class="bk_pop" href="#CDR0000062789_rl_1_35">35</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Sotos syndrome.</b> Sotos syndrome is characterized by cerebral gigantism and learning disability, ranging from mild to severe. Sotos syndrome is associated with behavioral problems, congenital cardiac anomalies, neonatal jaundice, and renal anomalies such as Wilms tumor, scoliosis, and seizures. </div><div class="half_rhythm">Mutations in the <i>NSD1</i> gene are the only known cause of Sotos syndrome.[<a class="bk_pop" href="#CDR0000062789_rl_1_36">36</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>9q22.3 microdeletion syndrome.</b> 9q22.3 microdeletion syndrome is characterized by craniofacial abnormalities, metopic craniosynostosis, hydrocephalus, macrosomia, and learning disabilities. </div><div class="half_rhythm">Of 44 described patients with 9q22.3 deletions, 7 patients developed Wilms tumor, and there was an association with overgrowth in 4 of those 7 patients. Although the size of the deletions was variable, all of them encompassed the <i>PTCH1</i> gene.[<a class="bk_pop" href="#CDR0000062789_rl_1_37">37</a>]; [<a class="bk_pop" href="#CDR0000062789_rl_1_38">38</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000561227/" class="def">Level of evidence: 3iii</a>] According to the authors of this study, surveillance for Wilms tumor should be considered in any patient with 9q22.3 microdeletion syndrome, especially in the presence of overgrowth.[<a class="bk_pop" href="#CDR0000062789_rl_1_38">38</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000561227/" class="def">Level of evidence: 3iii</a>] </div></li><li class="half_rhythm"><div class="half_rhythm"><b>Bloom syndrome.</b> Bloom syndrome is characterized by short stature and being thinner than other family members, sun-sensitive skin changes, and an increased risk of Wilms tumor. </div><div class="half_rhythm">Mutations in the <i>BLM</i> gene are the only known cause of Bloom syndrome.[<a class="bk_pop" href="#CDR0000062789_rl_1_39">39</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Li-Fraumeni syndrome.</b> Li-Fraumeni syndrome is a rare disorder that greatly increases the risk of developing several types of cancer, particularly in children and young adults.
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The cancers most often associated with Li-Fraumeni syndrome include breast cancer, osteosarcoma, soft tissue sarcoma, brain tumor, leukemia, adrenocortical carcinoma, and Wilms tumor. </div><div class="half_rhythm">The <i>TP53</i> gene mutation is present in most families with Li-Fraumeni syndrome. The <i>CHEK2</i> gene mutation is also known to cause Li-Fraumeni syndrome.[<a class="bk_pop" href="#CDR0000062789_rl_1_40">40</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Alagille syndrome.</b> Alagille syndrome includes congenital cardiopathy; facial dysmorphology; and vertebral, ocular, and renal abnormalities. It has been reported with Wilms tumor in two cases with identified mutations.[<a class="bk_pop" href="#CDR0000062789_rl_1_41">41</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Bohring-Opitz syndrome.</b> Bohring-Opitz syndrome is a rare genetic condition characterized by distinctive facial features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual posture, severe intellectual disability, and feeding issues. </div><div class="half_rhythm">The syndrome is associated with <i>ASXL1</i> mutations and an estimated 7% incidence of Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_42">42</a>]</div></li></ul></div></div><div id="CDR0000062789__1092"><h4>Nonsyndromic causes of Wilms tumor</h4><p id="CDR0000062789__1093">Nonsyndromic causes of Wilms tumor include the following:</p><ul id="CDR0000062789__1094"><li class="half_rhythm"><div class="half_rhythm"><b>Familial Wilms tumor.</b> Despite the number of genes that appear to be involved in the development of
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Wilms tumor, familial Wilms tumor is uncommon, with approximately 2% of patients
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having a positive family history of Wilms tumor. Siblings of children with Wilms tumor have a less-than-1% chance of developing Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_43">43</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_45">45</a>] The risk of Wilms
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tumor among offspring of persons who have had unilateral (sporadic)
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tumors is less than 2%.[<a class="bk_pop" href="#CDR0000062789_rl_1_46">46</a>] </div><div class="half_rhythm">Two familial Wilms tumor genes have been localized to <i>WT4</i> (17q12-q21) and <i>FWT2</i> (19q13.4).[<a class="bk_pop" href="#CDR0000062789_rl_1_47">47</a> -<a class="bk_pop" href="#CDR0000062789_rl_1_49">49</a>] Occasionally, Wilms tumor families have a germline mutation in <i>WT1</i>. In these families, most, but not all, family members have genitourinary tract malformations.[<a class="bk_pop" href="#CDR0000062789_rl_1_50">50</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_51">51</a>]</div><div class="half_rhythm">Inactivating mutations in <i>CTR9</i> have been identified in 3 of 35 Wilms tumor families. <i>CTR9</i> is located at 11p15.3 and is a key component of the polymerase-associated factor 1 (PAF1) complex, which has multiple roles in RNA polymerase II regulation and transcriptional elongation and is implicated in embryonic organogenesis.[<a class="bk_pop" href="#CDR0000062789_rl_1_52">52</a>] A few families with familial Wilms tumor have germline microdeletion or microinsertion mutations in the <i>H19</i> region of 11p15.3 that result in hypermethylation of the site.[<a class="bk_pop" href="#CDR0000062789_rl_1_53">53</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Constitutional 11p15 abnormalities.</b> Constitutional 11p15 abnormalities have been identified in lymphocyte DNA of 13 of 437 individuals (3%) with sporadic Wilms tumor without features of growth disorders, including 12% of bilateral cases. All were de novo abnormalities and appeared to be postzygotic, except for one novel microdeletion in a child whose mother had the mutation and was not affected; however, a younger brother with the microdeletion had Beckwith-Wiedemann syndrome. This suggests that constitutional 11p15 analysis should be considered in all individuals with Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_53">53</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Sporadic aniridia.</b> Sporadic aniridia may result from small germline deletions of one copy of the <i>PAX6</i> gene that includes part or all of the adjacent <i>WT1</i> gene but does not result in genitourinary abnormalities or intellectual disability (i.e., not obviously WAGR syndrome). Therefore, many patients with sporadic aniridia develop Wilms tumor and are candidates for genetic testing. The relative risk of Wilms tumor in sporadic aniridia is 67-fold.[<a class="bk_pop" href="#CDR0000062789_rl_1_54">54</a>] About one-half of individuals with sporadic aniridia and <i>PAX6</i> and <i>WT1</i> deletions develop Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_55">55</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Isolated hemihyperplasia.</b> Hemihyperplasia is an asymmetric overgrowth of one or more body parts and is associated with Wilms tumor. It can also be associated with other predisposition syndromes such as Beckwith-Wiedemann syndrome. Clinical signs may not be very evident, and hemihyperplasia may be noted after tumor diagnosis. </div><div class="half_rhythm">The overall Wilms tumor incidence was 5.9% in a study of 168 patients with isolated hemihyperplasia, although this result may have been affected by ascertainment bias.[<a class="bk_pop" href="#CDR0000062789_rl_1_56">56</a>] The prevalence is about 2.5% of children with Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_28">28</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_56">56</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Trisomy 18.</b>[<a class="bk_pop" href="#CDR0000062789_rl_1_57">57</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Fanconi anemia with biallelic mutations in <i>BRCA2</i> (<i>FANCD1</i>) or <i>PALB2</i> (<i>FANCN</i>).</b>
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<i>BRCA2</i> and <i>PALB2</i> play central roles in homologous recombination DNA repair. Biallelic mutations in either <i>BRCA2</i> or <i>PALB2</i> lead to Fanconi anemia and to increased risks of selected childhood cancers, including Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_58">58</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_60">60</a>]</div></li></ul></div></div><div id="CDR0000062789__1203"><h3>Genomics of Wilms Tumor</h3></div><div id="CDR0000062789__sm_CDR0000777841_13"><h3>Molecular Features of Wilms Tumor</h3><p id="CDR0000062789__sm_CDR0000777841_1254">Wilms tumor may arise during embryogenesis on the background of an otherwise genomically normal kidney, or it may arise from nongermline somatic genetic precursor lesions residing in histologically and functionally normal kidney tissue. Hypermethylation of <i>H19</i>, a known component of a subset of Wilms tumors, is a very common genetic abnormality found in these normal-appearing areas of precursor lesions.[<a class="bk_pop" href="#CDR0000062789_rl_1_61">61</a>]</p><p id="CDR0000062789__sm_CDR0000777841_75">One study performed genome-wide sequencing, mRNA and miRNA expression, DNA copy number, and methylation analysis on 117 Wilms tumors followed by targeted sequencing of 651 Wilms tumors.[<a class="bk_pop" href="#CDR0000062789_rl_1_62">62</a>] The tumors were selected for either favorable histology (FH) Wilms that had relapsed or those with diffuse anaplasia. The study showed the following:[<a class="bk_pop" href="#CDR0000062789_rl_1_62">62</a>]</p><ul id="CDR0000062789__sm_CDR0000777841_76"><li class="half_rhythm"><div>Wilms tumors commonly arise through more than one genetic event.</div></li><li class="half_rhythm"><div>Wilms tumors show differences in gene expression and methylation patterns with different genetic aberrations.</div></li><li class="half_rhythm"><div>Wilms tumors have a large number of candidate driver genes, most of which are mutated in less than 5% of Wilms tumors.</div></li><li class="half_rhythm"><div>Wilms tumors have recurrent mutations in genes with common functions, with most involved in either early renal development or epigenetic regulation (e.g., chromatin modifications, transcription elongation, and miRNA).</div></li></ul><p id="CDR0000062789__sm_CDR0000777841_15">Approximately one-third of Wilms tumor cases involve mutations in <i>WT1</i>, <i>CTNNB1</i>, or <i>WTX</i>.[<a class="bk_pop" href="#CDR0000062789_rl_1_63">63</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_64">64</a>] Another subset of Wilms tumor cases results from mutations in miRNA processing genes (miRNAPG), including <i>DROSHA</i>, <i>DGCR8</i>, <i>DICER1</i>, and <i>XPO5</i>.[<a class="bk_pop" href="#CDR0000062789_rl_1_65">65</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_68">68</a>] Other genes critical for early renal development that are recurrently mutated in Wilms tumor include <i>SIX1</i> and <i>SIX2</i> (transcription factors that play key roles in early renal development),[<a class="bk_pop" href="#CDR0000062789_rl_1_65">65</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_66">66</a>] <i>EP300</i>, <i>CREBBP</i>, and <i>MYCN</i>.[<a class="bk_pop" href="#CDR0000062789_rl_1_62">62</a>] Of the mutations in Wilms tumors, 30% to 50% appear to converge on the process of transcriptional elongation in renal development and include the genes <i>MLLT1</i>, <i>BCOR</i>, <i>MAP3K4</i>, <i>BRD7</i>, and <i>HDAC4</i>.[<a class="bk_pop" href="#CDR0000062789_rl_1_62">62</a>] Anaplastic Wilms tumor is characterized by the presence of <i>TP53</i> mutations.</p><p id="CDR0000062789__sm_CDR0000777841_21">Elevated rates of Wilms tumor are observed in patients with a number of genetic disorders, including WAGR (Wilms tumor, aniridia, genitourinary anomalies, and mental retardation) syndrome, Beckwith-Wiedemann syndrome, hemihypertrophy, Denys-Drash syndrome, and Perlman syndrome.[<a class="bk_pop" href="#CDR0000062789_rl_1_69">69</a>] Other genetic causes that have been observed in familial Wilms tumor cases include germline mutations in <i>REST</i> and <i>CTR9</i>.[<a class="bk_pop" href="#CDR0000062789_rl_1_52">52</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_70">70</a>]</p><p id="CDR0000062789__sm_CDR0000777841_22">The genomic and genetic characteristics of Wilms tumor are summarized below.</p><div id="CDR0000062789__sm_CDR0000777841_16"><h4><i>WT1</i> gene</h4><p id="CDR0000062789__sm_CDR0000777841_18">The
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<i>WT1</i> gene is located on the short arm of chromosome 11 (11p13). WT1 is a transcription factor that is required for normal genitourinary development and is important for differentiation of the renal blastema.[<a class="bk_pop" href="#CDR0000062789_rl_1_71">71</a>] <i>WT1</i> mutations are observed in 10% to 20% of cases of sporadic Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_63">63</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_71">71</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_72">72</a>] </p><p id="CDR0000062789__sm_CDR0000777841_65">Wilms tumor with a <i>WT1</i> mutation is characterized by the following:</p><ul id="CDR0000062789__sm_CDR0000777841_19"><li class="half_rhythm"><div>Evidence of WNT pathway activation by activating mutations in the <i>CTNNB1</i> gene is common.[<a class="bk_pop" href="#CDR0000062789_rl_1_72">72</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_74">74</a>]</div></li><li class="half_rhythm"><div>Loss of heterozygosity (LOH) at 11p15 is commonly observed, as paternal uniparental disomy for chromosome 11 represents a common mechanism for losing the remaining normal <i>WT1</i> allele.[<a class="bk_pop" href="#CDR0000062789_rl_1_72">72</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_75">75</a>]</div></li><li class="half_rhythm"><div>Nephrogenic rests are benign foci of embryonal kidney cells that abnormally persist into postnatal life. Intralobar nephrogenic rests occur in approximately 20% of Wilms tumor cases. They are observed at high rates in cases with genetic syndromes that have <i>WT1</i> mutations such as WAGR and Denys-Drash syndromes.[<a class="bk_pop" href="#CDR0000062789_rl_1_76">76</a>] Intralobar nephrogenic rests are also observed in cases with sporadic <i>WT1</i> and <i>MLLT1</i> mutations.[<a class="bk_pop" href="#CDR0000062789_rl_1_77">77</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_78">78</a>] </div></li><li class="half_rhythm"><div><i>WT1</i> germline mutations are uncommon (2%–4%) in nonsyndromic Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_51">51</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_79">79</a>]</div></li><li class="half_rhythm"><div><i>WT1</i> mutations and 11p15 LOH were associated with relapse in patients with very low-risk Wilms tumor in one study of 56 patients who did not receive chemotherapy.[<a class="bk_pop" href="#CDR0000062789_rl_1_80">80</a>] These findings need validation but may provide biomarkers for stratifying patients in the future.</div></li></ul><p id="CDR0000062789__sm_CDR0000777841_20">Germline <i>WT1</i> mutations are more common in children with Wilms tumor <b>and</b> one of the following:</p><ul id="CDR0000062789__sm_CDR0000777841_23"><li class="half_rhythm"><div>WAGR syndrome, Denys-Drash syndrome,[<a class="bk_pop" href="#CDR0000062789_rl_1_18">18</a>] or Frasier syndrome.[<a class="bk_pop" href="#CDR0000062789_rl_1_15">15</a>]</div></li><li class="half_rhythm"><div>Genitourinary anomalies, including hypospadias and cryptorchidism.</div></li><li class="half_rhythm"><div>Bilateral Wilms tumor.</div></li><li class="half_rhythm"><div>Unilateral Wilms tumor with nephrogenic rests in the contralateral kidney.</div></li><li class="half_rhythm"><div>Stromal and rhabdomyomatous differentiation.</div></li></ul><p id="CDR0000062789__sm_CDR0000777841_24">Germline <i>WT1</i> point mutations produce genetic syndromes that are characterized by nephropathy, 46XY disorder of sex development, and varying risks of Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_81">81</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_82">82</a>] Syndromic conditions with germline <i>WT1</i> mutations include WAGR syndrome, Denys-Drash syndrome,[<a class="bk_pop" href="#CDR0000062789_rl_1_18">18</a>] and Frasier syndrome.[<a class="bk_pop" href="#CDR0000062789_rl_1_15">15</a>]</p><ul id="CDR0000062789__sm_CDR0000777841_25"><li class="half_rhythm"><div class="half_rhythm"><b>WAGR syndrome.</b> Children with WAGR syndrome are at high risk (approximately 50%) of developing Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_5">5</a>] WAGR syndrome results from deletions at chromosome 11p13 that involve a set of contiguous genes that include the <i>WT1</i> and <i>PAX6</i> genes. </div><div class="half_rhythm">Inactivating mutations or deletions in the <i>PAX6</i> gene lead to aniridia, while deletion of <i>WT1</i> confers the increased risk of Wilms tumor. Loss of the <i>LMO2</i> gene has been associated with a more frequent development of Wilms tumor in patients with congenital aniridia and WAGR-region deletions.[<a class="bk_pop" href="#CDR0000062789_rl_1_83">83</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000561227/" class="def">Level of evidence: 3iii</a>] Sporadic aniridia in which <i>WT1</i> is not deleted is not associated with increased risk of Wilms tumor. Accordingly, children with familial aniridia, generally occurring for many generations, and without renal abnormalities, have a normal <i>WT1</i> gene and are not at an increased risk of Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_28">28</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_84">84</a>] </div><div class="half_rhythm">Wilms tumor in children with WAGR syndrome is characterized by an excess of bilateral disease, intralobar nephrogenic rests, early age at diagnosis, and stromal-predominant histology in FH tumors.[<a class="bk_pop" href="#CDR0000062789_rl_1_14">14</a>] The intellectual disability in WAGR syndrome may be secondary to deletion of other genes, including <i>SLC1A2</i> or <i>BDNF</i>.[<a class="bk_pop" href="#CDR0000062789_rl_1_53">53</a>]</div></li></ul><ul id="CDR0000062789__sm_CDR0000777841_28"><li class="half_rhythm"><div class="half_rhythm"><b>Denys-Drash syndrome.</b> Denys-Drash syndrome is characterized by nephrotic syndrome caused by diffuse mesangial sclerosis, XY pseudohermaphroditism, and increased risk of Wilms tumor (>90%). </div><div class="half_rhythm"><i>WT1</i> mutations in Denys-Drash syndrome are most often missense mutations in exons 8 and 9, which code for the DNA binding region of <i>WT1</i>.[<a class="bk_pop" href="#CDR0000062789_rl_1_18">18</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Frasier syndrome.</b> Frasier syndrome is characterized by progressive nephropathy caused by focal segmental glomerulosclerosis, gonadoblastoma, and XY pseudohermaphroditism.</div><div class="half_rhythm">
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<i>WT1</i> mutations in Frasier syndrome typically occur in intron 9 at the <i>KTS site</i>, and create an alternative splicing variant, thereby preventing production of the usually more abundant WT1 +KTS isoform.[<a class="bk_pop" href="#CDR0000062789_rl_1_20">20</a>]</div></li></ul><p id="CDR0000062789__sm_CDR0000777841_81">Studies evaluating genotype/phenotype correlations of <i>WT1</i> mutations have shown that the risk of Wilms tumor is highest for truncating mutations (14 of 17 cases, 82%) and lower for missense mutations (27 of 67 cases, 42%). The risk is lowest for KTS splice site mutations (1 of 27 cases, 4%).[<a class="bk_pop" href="#CDR0000062789_rl_1_81">81</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_82">82</a>] Bilateral Wilms tumor was more common in cases with <i>WT1</i>-truncating mutations (9 of 14 cases) than in cases with <i>WT1</i> missense mutations (3 of 27 cases).[<a class="bk_pop" href="#CDR0000062789_rl_1_81">81</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_82">82</a>] These genomic studies confirm previous estimates of elevated risk of Wilms tumor for children with Denys-Drash syndrome and low risk of Wilms tumor for children with Frasier syndrome.</p></div><div id="CDR0000062789__sm_CDR0000777841_33"><h4><i>CTNNB1</i> gene</h4><p id="CDR0000062789__sm_CDR0000777841_34"><i>CTNNB1</i> is one of the most commonly mutated genes in Wilms tumor, reported to occur in 15% of patients with Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_62">62</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_64">64</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_72">72</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_74">74</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_85">85</a>] These <i>CTNNB1</i> mutations result in activation of the WNT pathway, which plays a prominent role in the developing kidney.[<a class="bk_pop" href="#CDR0000062789_rl_1_86">86</a>] <i>CTNNB1</i> mutations commonly occur with <i>WT1</i> mutations, and most cases of Wilms tumor with <i>WT1</i> mutations have a concurrent <i>CTNNB1</i> mutation.[<a class="bk_pop" href="#CDR0000062789_rl_1_72">72</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_74">74</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_85">85</a>] Activation of beta-catenin in the presence of intact WT1 protein appears to be inadequate to promote tumor development because <i>CTNNB1</i> mutations are rarely found in the absence of a <i>WT1</i> or <i>WTX</i> mutation, except when associated with a <i>MLLT1</i> mutation.[<a class="bk_pop" href="#CDR0000062789_rl_1_64">64</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_87">87</a>] <i>CTNNB1</i> mutations appear to be late events in Wilms tumor development because they are found in tumors but not in nephrogenic rests.[<a class="bk_pop" href="#CDR0000062789_rl_1_77">77</a>]</p></div><div id="CDR0000062789__sm_CDR0000777841_35"><h4><i>WTX</i> gene on the X chromosome</h4><p id="CDR0000062789__sm_CDR0000777841_36"><i>WTX</i>, which is also called <i>AMER1</i>, is located on the X chromosome at Xq11.1. It is altered in 15% to 20% of Wilms tumor cases.[<a class="bk_pop" href="#CDR0000062789_rl_1_63">63</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_64">64</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_72">72</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_88">88</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_89">89</a>] Germline mutations in <i>WTX</i> cause an X-linked sclerosing bone dysplasia, osteopathia striata congenita with cranial sclerosis (<a href="http://omim.org/entry/300373" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">MIM300373</a>).[<a class="bk_pop" href="#CDR0000062789_rl_1_90">90</a>] Despite having germline <i>WTX</i> mutations, individuals with osteopathia striata congenita are not predisposed to tumor development.[<a class="bk_pop" href="#CDR0000062789_rl_1_90">90</a>] The WTX protein appears to be involved in both the degradation of beta-catenin and in the intracellular distribution of APC protein.[<a class="bk_pop" href="#CDR0000062789_rl_1_87">87</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_91">91</a>] <i>WTX</i> is most commonly altered by deletions involving part or all of the <i>WTX</i> gene, with deleterious point mutations occurring less commonly.[<a class="bk_pop" href="#CDR0000062789_rl_1_63">63</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_72">72</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_88">88</a>] Most Wilms tumor cases with <i>WTX</i> alterations have epigenetic 11p15 abnormalities.[<a class="bk_pop" href="#CDR0000062789_rl_1_72">72</a>]
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</p><p id="CDR0000062789__sm_CDR0000777841_71"><i>WTX</i> alterations are equally distributed between males and females, and <i>WTX</i> inactivation has no apparent effect on clinical presentation or prognosis.[<a class="bk_pop" href="#CDR0000062789_rl_1_63">63</a>]</p></div><div id="CDR0000062789__sm_CDR0000777841_37"><h4>Imprinting cluster regions (ICRs) on chromosome 11p15 (<i>WT2</i>) and Beckwith-Wiedemann syndrome</h4><p id="CDR0000062789__sm_CDR0000777841_38">A second Wilms tumor locus, <i>WT2</i>, maps to an imprinted region of chromosome 11p15.5; when it is a germline mutation, it causes Beckwith-Wiedemann syndrome. About 3% of children with Wilms tumor have germline epigenetic or genetic changes at the 11p15.5 growth regulatory locus without any clinical manifestations of overgrowth. Like children with Beckwith-Wiedemann syndrome, these children have an increased incidence of bilateral Wilms tumor or familial Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_53">53</a>]</p><p id="CDR0000062789__sm_CDR0000777841_1251">Approximately one-fifth of patients with Beckwith-Wiedemann syndrome who develop Wilms tumor present with bilateral disease, and metachronous bilateral disease is also observed.[<a class="bk_pop" href="#CDR0000062789_rl_1_28">28</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_30">30</a>] The prevalence of Beckwith-Wiedemann syndrome is about 1% among children with Wilms tumor reported to the National Wilms Tumor Study (NWTS).[<a class="bk_pop" href="#CDR0000062789_rl_1_3">3</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_30">30</a>]</p><p id="CDR0000062789__sm_CDR0000777841_39">Approximately 80% of patients with Beckwith-Wiedemann syndrome have a molecular defect of the 11p15 domain.[<a class="bk_pop" href="#CDR0000062789_rl_1_92">92</a>] Various molecular mechanisms underlying Beckwith-Wiedemann syndrome have been identified. Some of these abnormalities are genetic (germline mutations of the maternal allele of <i>CDKN1C</i>, paternal uniparental isodisomy of 11p15, or duplication of part of the 11p15 domain) but are more frequently epigenetic (loss of methylation of the maternal <i>ICR2/KvDMR1</i> or gain of methylation of the maternal <i>ICR1</i>).[<a class="bk_pop" href="#CDR0000062789_rl_1_53">53</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_93">93</a>]</p><p id="CDR0000062789__sm_CDR0000777841_40">Several candidate genes at the <i>WT2</i> locus comprise the two independent imprinted domains <i>IGF2/H19</i> and <i>KIP2/LIT1</i>.[<a class="bk_pop" href="#CDR0000062789_rl_1_93">93</a>] LOH, which exclusively affects the maternal chromosome, has the effect of upregulating paternally active genes and silencing maternally active ones. A loss or switch of the imprint for genes (change in methylation status) in this region has also been frequently observed and results in the same functional aberrations.[<a class="bk_pop" href="#CDR0000062789_rl_1_53">53</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_92">92</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_93">93</a>]</p><p id="CDR0000062789__sm_CDR0000777841_41">A relationship between epigenotype and phenotype has been shown in Beckwith-Wiedemann syndrome, with a different rate of cancer in Beckwith-Wiedemann syndrome according to the type of alteration of the 11p15 region.[<a class="bk_pop" href="#CDR0000062789_rl_1_94">94</a>]</p><p id="CDR0000062789__sm_CDR0000777841_1228">The following four main molecular subtypes of Beckwith-Wiedemann syndrome are characterized by specific genotype-phenotype correlations:</p><ol id="CDR0000062789__sm_CDR0000777841_1250"><li class="half_rhythm"><div><b>ICR1 gain of methylation (ICR1-GoM).</b> Five percent to 10% of cases are caused by telomeric ICR1-GoM, which causes both biallelic expression of the <i>IGF2</i> gene (normally expressed by the paternal allele only) and reduced expression of the oncosuppressor <i>H19</i> gene. The incidence of Wilms tumor is 22.8%.[<a class="bk_pop" href="#CDR0000062789_rl_1_95">95</a>]</div></li><li class="half_rhythm"><div><b>ICR2 loss of methylation (ICR2-LoM).</b> Fifty percent of cases with Beckwith-Wiedemann syndrome are caused by ICR2-LoM, resulting in reduced expression of the <i>CDKN1C</i> gene, normally expressed by the maternal chromosome only. Tumor incidence is very low (2.5%).[<a class="bk_pop" href="#CDR0000062789_rl_1_95">95</a>]</div></li><li class="half_rhythm"><div><b>Uniparental disomy (UPD).</b> Altered expression at both imprinted gene clusters is observed in mosaic UPD of chromosome 11p15.5, accounting for 20% to 25% of the cases. The incidence of Wilms tumor is 6.2%, followed by hepatoblastoma (4.7%) and adrenal carcinoma (1.5%).[<a class="bk_pop" href="#CDR0000062789_rl_1_95">95</a>] Fewer than 1% of cases with Beckwith-Wiedemann syndrome are caused by chromosomal rearrangements involving the 11p15 region.</div></li><li class="half_rhythm"><div><b><i>CDKN1C</i> mutations.</b> Maternally inheritable <i>CDKN1C</i> loss-of-function mutations account for approximately 5% of the cases. This type is associated with a 4.3% incidence of neuroblastoma.[<a class="bk_pop" href="#CDR0000062789_rl_1_95">95</a>]</div></li></ol><p id="CDR0000062789__sm_CDR0000777841_1252">Other tumors such as neuroblastoma or hepatoblastoma were reported in patients with paternal 11p15 isodisomy.[<a class="bk_pop" href="#CDR0000062789_rl_1_22">22</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_26">26</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_96">96</a>] For patients with Beckwith-Wiedemann syndrome, the relative risk of developing hepatoblastoma is 2,280 times that of the general population.[<a class="bk_pop" href="#CDR0000062789_rl_1_30">30</a>]</p><p id="CDR0000062789__sm_CDR0000777841_42">Loss of imprinting or gene methylation is rarely found at other loci, supporting the specificity of loss of imprinting at 11p15.5.[<a class="bk_pop" href="#CDR0000062789_rl_1_97">97</a>] Interestingly, Wilms tumor in Asian children, which occurs at a lower incidence than in European children, is not associated with either nephrogenic rests or <i>IGF2</i> loss of imprinting.[<a class="bk_pop" href="#CDR0000062789_rl_1_98">98</a>]</p></div><div id="CDR0000062789__sm_CDR0000777841_44"><h4>Other genes and chromosomal alterations</h4><p id="CDR0000062789__sm_CDR0000777841_45">Additional genes and chromosomal alterations that have been implicated in the pathogenesis and biology of Wilms tumor include the following:</p><ul id="CDR0000062789__sm_CDR0000777841_46"><li class="half_rhythm"><div class="half_rhythm"><b>1q.</b> Gain of chromosome 1q is associated with an inferior outcome and is the single most powerful predictor of outcome.[<a class="bk_pop" href="#CDR0000062789_rl_1_99">99</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_100">100</a>] Gain of chromosome 1q is one of the most common cytogenetic abnormalities in Wilms tumor and is observed in approximately 30% of tumors. </div><div class="half_rhythm">In an analysis of FH Wilms tumor from 1,114 patients from <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5 (COG-Q9401/NCT00002611)</a>, 28% of the tumors displayed 1q gain.[<a class="bk_pop" href="#CDR0000062789_rl_1_99">99</a>] <ul id="CDR0000062789__sm_CDR0000777841_64"><li class="half_rhythm"><div>The 8-year event-free survival (EFS) rate was 77% for patients with 1q gain and 90% for those lacking 1q gain (<i>P</i> < .001). Within each disease stage, 1q gain was associated with inferior EFS. </div></li><li class="half_rhythm"><div>The 8-year overall survival (OS) rate was 88% for those with 1q gain and 96% for those lacking 1q gain (<i>P</i> < .001). OS was significantly inferior in cases with stage I disease (<i>P</i> < .0015) and stage IV disease (<i>P</i> = .011).</div></li></ul></div></li><li class="half_rhythm"><div class="half_rhythm"><b>16q and 1p.</b> Additional tumor-suppressor or tumor-progression genes may lie on chromosomes 16q and 1p, as evidenced by LOH for these regions in 17% and 11% of Wilms tumor cases, respectively.[<a class="bk_pop" href="#CDR0000062789_rl_1_101">101</a>]<dl id="CDR0000062789__sm_CDR0000777841_51" class="temp-labeled-list"><dt>-</dt><dd><p class="no_top_margin"> In large NWTS studies, patients with tumor-specific loss of these loci had significantly worse relapse-free survival and OS rates. Combined loss of 1p and 16q are used to select FH Wilms tumor patients for more aggressive therapy in the current Children's Oncology Group (COG) study. However, a U.K. study of more than 400 patients found no significant association between 1p deletion and poor prognosis, but a poor prognosis was associated with 16q LOH.[<a class="bk_pop" href="#CDR0000062789_rl_1_102">102</a>] </p></dd><dt>-</dt><dd><p class="no_top_margin">An Italian study of 125 patients, using treatment quite similar to that in the COG study, found significantly worse prognosis in those with 1p deletions but not 16q deletions.[<a class="bk_pop" href="#CDR0000062789_rl_1_103">103</a>] </p></dd></dl></div><div class="half_rhythm">These conflicting results may arise from the greater prognostic significance of 1q gain described above. LOH of 16q and 1p loses significance as independent prognostic markers in the presence of 1q gain. However, in the absence of 1q gain, LOH of 16q and 1p retains their adverse prognostic impact.[<a class="bk_pop" href="#CDR0000062789_rl_1_99">99</a>] The LOH of 16q and 1p appears to arise from complex chromosomal events that result in 1q LOH or 1q gain. The change in 1q appears to be the critical tumorigenic genetic event.[<a class="bk_pop" href="#CDR0000062789_rl_1_104">104</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>miRNAPG.</b> Mutations in selected miRNAPG are observed in approximately 20% of Wilms tumor cases and appear to perpetuate the progenitor state.[<a class="bk_pop" href="#CDR0000062789_rl_1_62">62</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_65">65</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_68">68</a>] The products of these genes direct the maturation of miRNAs from the initial pri-miRNA transcripts to functional cytoplasmic miRNAs (refer to Figure 1).[<a class="bk_pop" href="#CDR0000062789_rl_1_105">105</a>] The most commonly mutated miRNAPG is <i>DROSHA</i>, with a recurrent mutation (E1147K) affecting a metal-binding residue of the RNase IIIb domain, representing about 80% of <i>DROSHA</i>-mutated tumors. Other miRNAPG that are mutated in Wilms tumor include <i>DGCR8</i>, <i>DICER1</i>, <i>TARBP2</i>, <i>DIS3L2</i>, and <i>XPO5</i>. These mutations are generally mutually exclusive, and they appear to be deleterious and result in impaired expression of tumor-suppressing miRNAs. A striking sex bias was noted in mutations for <i>DGCR8</i> (located on chromosome 22q11), with 38 of 43 cases (88%) arising in girls.[<a class="bk_pop" href="#CDR0000062789_rl_1_65">65</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_66">66</a>]</div><div class="half_rhythm">Germline mutations in miRNAPG are observed for <i>DICER1</i> and <i>DIS3L2</i>, with mutations in the former causing DICER1 syndrome and mutations in the latter causing Perlman syndrome. <ul id="CDR0000062789__sm_CDR0000777841_72"><li class="half_rhythm"><div class="half_rhythm">DICER1 syndrome is typically caused by inherited truncating mutations in <i>DICER1</i>, with tumor formation following acquisition of a missense mutation in a domain of the remaining allele of <i>DICER1</i> (the RNase IIIb domain) responsible for processing miRNAs derived from the 5p arms of pre-miRNAs.[<a class="bk_pop" href="#CDR0000062789_rl_1_106">106</a>] Tumors associated with DICER1 syndrome include pleuropulmonary blastoma, cystic nephroma, ovarian sex cord–stromal tumors, multinodular goiter, and embryonal rhabdomyosarcoma.[<a class="bk_pop" href="#CDR0000062789_rl_1_106">106</a>] Wilms tumor is an uncommon presentation of the DICER1 syndrome. In one study, three families with DICER1 syndrome included children with Wilms tumor, with two of the Wilms tumor cases showing the typical second <i>DICER1</i> mutation in the RNase IIIb domain.[<a class="bk_pop" href="#CDR0000062789_rl_1_107">107</a>] Another study identified <i>DICER1</i> mutations in 2 of 48 familial Wilms tumor families.[<a class="bk_pop" href="#CDR0000062789_rl_1_108">108</a>] Large sequencing studies of Wilms tumor cohorts have also observed occasional cases with <i>DICER1</i> mutations.[<a class="bk_pop" href="#CDR0000062789_rl_1_66">66</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_67">67</a>]</div></li><li class="half_rhythm"><div class="half_rhythm">Perlman syndrome is a rare overgrowth disorder caused by mutations in <i>DIS3L2</i>, which encodes a ribonuclease that is responsible for degrading pre-let-7 miRNA.[<a class="bk_pop" href="#CDR0000062789_rl_1_33">33</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_109">109</a>] The prognosis of Perlman syndrome is poor, with a high neonatal mortality rate. In a survey of published cases of Perlman syndrome (N = 28), in infants who survived beyond the neonatal period, approximately two-thirds developed Wilms tumor, and all patients showed developmental delay. Fetal macrosomia, ascites, and polyhydramnios are frequent manifestations.[<a class="bk_pop" href="#CDR0000062789_rl_1_110">110</a>]</div><div class="half_rhythm"><div id="CDR0000062789__sm_CDR0000777841_55" class="figure bk_fig"><div class="graphic"><img src="/books/NBK65842.23/bin/CDR0000777941.jpg" alt="Diagram showing the miRNA processing pathway, which is commonly mutated in Wilms' tumor." /></div><div class="caption"><p>Figure 1. The miRNA processing pathway is commonly mutated in Wilms tumor. Expression of mature miRNA is initiated by RNA polymerase–mediated transcription of DNA-encoded sequences into pri-miRNA, which form a long double-stranded hairpin. This structure is then cleaved by a complex of Drosha and DGCR8 into a smaller pre-miRNA hairpin, which is exported from the nucleus and then cleaved by Dicer (an RNase) and TRBP (with specificity for dsRNA) to remove the hairpin loop and leave two single-stranded miRNAs. The functional strand binds to Argonaute (Ago2) proteins into the RNA-induced silencing complex (RISC), where it guides the complex to its target mRNA, while the nonfunctional strand is degraded. Targeting of mRNAs by this method results in mRNA silencing by mRNA cleavage, translational repression, or deadenylation. Let-7 miRNAs are a family of miRNAs highly expressed in ESCs with tumor suppressor properties. In cases in which LIN28 is overexpressed, LIN28 binds to pre-Let-7 miRNA, preventing DICER from binding and resulting in LIN28-activated polyuridylation by TUT4 or TUT7, causing reciprocal DIS3L2-mediated degradation of Let-7 pre-miRNAs. Genes involved in miRNA processing that have been associated with Wilms tumor are highlighted in blue (inactivating) and green (activating) and include DROSHA, DGCR8, XPO5 (encoding exportin-5), DICER1, TARBP2, DIS3L2, and LIN28. Copyright © 2015 <a href="http://genesdev.cshlp.org/content/29/5/467.full" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Hohenstein et al.; Published by Cold Spring Harbor Laboratory Press. Genes Dev. 2015 Mar 1; 29(5): 467–482. doi: 10.1101/gad.256396.114</a>. This article is distributed exclusively by Cold Spring Harbor Laboratory Press under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at <a href="http://creativecommons.org/licenses/by-nc/4.0/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">http://creativecommons.org/licenses/by-nc/4.0/</a>.
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</p></div></div></div></li></ul></div></li><li class="half_rhythm"><div class="half_rhythm"><b><i>SIX1</i> and <i>SIX2</i>.</b>
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<i>SIX1</i> and <i>SIX2</i> are highly homologous transcription factors that play key roles in early renal development and are expressed in the metanephric mesenchyme, where they maintain the mesenchymal progenitor population. The frequency of <i>SIX1</i> mutations is 3% to 4% in Wilms tumor, and the frequency of <i>SIX2</i> mutations in Wilms tumor is 1% to 3%.[<a class="bk_pop" href="#CDR0000062789_rl_1_65">65</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_66">66</a>] Virtually all <i>SIX1</i> and <i>SIX2</i> mutations are in exon 1 and result in a glutamine-to-arginine mutation at position 177. Mutations in <i>WT1</i>, <i>WTX</i>, and <i>CTNNB1</i> are infrequent in cases with <i>SIX1/SIX2</i> or miRNAPG mutations. Conversely, <i>SIX1/SIX2</i> mutations and miRNAPG mutations tend to occur together. In Wilms tumor, <i>SIX1</i> and <i>SIX2</i> mutations are associated with the high-risk blastemal subtype and with the presence of undifferentiated blastema in chemotherapy-naïve samples.[<a class="bk_pop" href="#CDR0000062789_rl_1_65">65</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_66">66</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b><i>MLLT1</i>.</b> Approximately 4% of Wilms tumor cases have mutations in the highly conserved YEATS domain of <i>MLLT1</i> (<i>ENL</i>), a gene known to be involved in transcriptional elongation by RNA polymerase II during early development.[<a class="bk_pop" href="#CDR0000062789_rl_1_78">78</a>] The mutant MLLT1 protein shows altered binding to acetylated histone tails. Patients with <i>MLLT1</i>-mutant tumors present at a younger age and have a high prevalence of precursor intralobar nephrogenic rests, supporting a model whereby activating <i>MLLT1</i> mutations early in renal development result in the development of Wilms tumor.</div></li><li class="half_rhythm"><div class="half_rhythm"><b><i>TP53</i> (tumor suppressor gene).</b> Most anaplastic Wilms tumor cases show mutations in the <i>TP53</i> tumor suppressor gene.[<a class="bk_pop" href="#CDR0000062789_rl_1_111">111</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_113">113</a>] <i>TP53</i> may be useful as an unfavorable prognostic marker.[<a class="bk_pop" href="#CDR0000062789_rl_1_111">111</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_112">112</a>] </div><div class="half_rhythm">In a study of 118 prospectively identified patients with diffuse anaplastic Wilms tumor registered on the NWTS-5 trial, 57 patients (48%) demonstrated <i>TP53</i> mutations, 13 patients (11%) demonstrated <i>TP53</i> segmental copy number loss without mutation, and 48 patients (41%) lacked both (wild-type <i>TP53</i> [wt<i>TP53</i>]). All <i>TP53</i> mutations were detected by sequencing alone. Patients with stage III or stage IV disease with wt<i>TP53</i> had a significantly lower relapse rate and mortality rate than did patients with <i>TP53</i> abnormalities (<i>P</i> = .00006 and <i>P</i> = .00007, respectively). The TP53 status had no effect on patients with stage I or stage II tumors.[<a class="bk_pop" href="#CDR0000062789_rl_1_114">114</a>]<ul id="CDR0000062789__sm_CDR0000777841_1258"><li class="half_rhythm"><div> In-depth analysis of a subset of 39 patients with diffuse anaplastic Wilms tumor showed that 7 patients (18%) were wt<i>TP53</i>. These wt<i>TP53</i> tumors demonstrated gene expression evidence of p53 pathway activation. Retrospective pathology review of wt<i>TP53</i> tumors revealed no or very low volume of anaplasia in six of seven tumors. These data support the key role of TP53 loss in the development of anaplasia in Wilms tumor and support its significant clinical influence in patients who have residual anaplastic disease after surgery.[<a class="bk_pop" href="#CDR0000062789_rl_1_114">114</a>]</div></li></ul></div></li><li class="half_rhythm"><div class="half_rhythm"><b><i>FBXW7</i>.</b>
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<i>FBXW7</i>, a ubiquitin ligase component, is a gene that has been identified as recurrently mutated at low rates in Wilms tumor. Mutations of this gene have been associated with epithelial-type tumor histology.[<a class="bk_pop" href="#CDR0000062789_rl_1_115">115</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>9q22.3 microdeletion syndrome.</b> Patients with 9q22.3 microdeletion syndrome have an increased risk of Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_37">37</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_116">116</a>] The chromosomal region with germline deletion includes <i>PTCH1</i>, the gene that is mutated in Gorlin syndrome (nevoid basal cell carcinoma syndrome associated with osteosarcoma). 9q22.3 microdeletion syndrome is characterized by the clinical findings of Gorlin syndrome, as well as developmental delay and/or intellectual disability, metopic craniosynostosis, obstructive hydrocephalus, prenatal and postnatal macrosomia, and seizures.[<a class="bk_pop" href="#CDR0000062789_rl_1_116">116</a>] Five patients who presented with Wilms tumor in the context of a constitutional 9q22.3 microdeletion have been reported.[<a class="bk_pop" href="#CDR0000062789_rl_1_37">37</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_117">117</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_118">118</a>] </div></li><li class="half_rhythm"><div class="half_rhythm"><b><i>MYCN</i>.</b>
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<i>MYCN</i> copy number gain was observed in approximately 13% of Wilms tumor cases, and it was more common in anaplastic cases (7 of 23 cases, 30%) than in nonanaplastic cases (11.2%).[<a class="bk_pop" href="#CDR0000062789_rl_1_119">119</a>] Activating mutations at codon 44 (p.P44L) were identified in approximately 4% of Wilms tumor cases.[<a class="bk_pop" href="#CDR0000062789_rl_1_119">119</a>] Germline copy number gain at <i>MYCN</i> has been reported in a bilateral Wilms tumor case, and germline <i>MYCN</i> duplication was also reported for a child with prenatal bilateral nephroblastomatosis and a family history of nephroblastoma.[<a class="bk_pop" href="#CDR0000062789_rl_1_120">120</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b><i>CTR9</i>.</b> Inactivating <i>CTR9</i> germline mutations were identified in 4 of 36 familial Wilms tumor pedigrees.[<a class="bk_pop" href="#CDR0000062789_rl_1_52">52</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_121">121</a>] <i>CTR9</i>, which is located at chromosome 11p15.3, is a key component of the polymerase-associated factor 1 complex (PAF1c), which has multiple roles in RNA polymerase II regulation and is implicated in embryonic organogenesis and maintenance of embryonic stem cell pluripotency.</div></li><li class="half_rhythm"><div class="half_rhythm"><b><i>REST</i>.</b> Inactivating germline mutations in <i>REST</i> (encoding RE1-silencing transcription factor) were identified in four familial Wilms tumor pedigrees.[<a class="bk_pop" href="#CDR0000062789_rl_1_70">70</a>] REST is a transcriptional repressor that functions in cellular differentiation and embryonic development. Most <i>REST</i> mutations clustered within the portion of REST encoding the DNA-binding domain, and functional analyses showed that these mutations compromise REST transcriptional repression. When screened for <i>REST</i> mutations, 9 of 519 individuals with Wilms tumor who had no history of relatives with the disease tested positive for the mutation; some had parents who also tested positive.[<a class="bk_pop" href="#CDR0000062789_rl_1_70">70</a>] These observations indicate that <i>REST</i> is a Wilms tumor predisposition gene associated with approximately 2% of Wilms tumor.</div></li></ul><p id="CDR0000062789__sm_CDR0000777841_53">Figure 2 summarizes the genomic landscape of a selected cohort of Wilms tumor patients selected because they experienced relapse despite showing favorable histology (FH).[<a class="bk_pop" href="#CDR0000062789_rl_1_78">78</a>] The 75 FH Wilms tumor cases were clustered by unsupervised analysis of gene expression data, resulting in six clusters. Five of six <i>MLLT1</i>-mutant tumors with available gene expression data were in cluster 3, and two were accompanied by <i>CTNNB1</i> mutations. This cluster also contained four tumors with a mutation or small segment deletion of <i>WT1</i>, all of which also had either a mutation of <i>CTNNB1</i> or small segment deletion or mutation of <i>WTX</i>. It also contained a substantial number of tumors with retention of imprinting of 11p15 (including all <i>MLLT1</i>-mutant tumors). The miRNAPG-mutated cases clustered together and were mutually exclusive with both <i>MLLT1</i> and with <i>WT1</i>/<i>WTX</i>/<i>CTNNB1</i>-mutated cases.</p><a id="CDR0000062789__sm_CDR0000777841_56"></a><div id="CDR0000062789__sm_CDR0000777841_57" class="figure bk_fig"><div class="graphic"><img src="/books/NBK65842.23/bin/CDR0000777942.jpg" alt="Chart showing unsupervised analysis of gene expression data for clinically distinctive favorable histology Wilms tumor." /></div><div class="caption"><p>Figure 2. Unsupervised analysis of gene expression data. Non-negative Matrix Factorization (NMF) analysis of 75 FH Wilms tumor resulted in six clusters. Five of six <i>MLLT1</i> mutant tumors with available gene expression data occurred in NMF cluster 3, and two were accompanied by <i>CTNNB1</i> mutations. This cluster also contained a substantial number of tumors with retention of imprinting of 11p15 (including all <i>MLLT1</i>-mutant tumors), in contrast to other clusters, where most cases showed 11p15 loss of heterozygosity or retention of imprinting. Almost all miRNAPG-mutated cases were in NMF cluster 2, and most <i>WT1</i>, <i>WTX</i>, and <i>CTNNB1</i> mutations were in NMF clusters 3 and 4. Copyright © 2015 <a href="http://www.nature.com/ncomms/2015/151204/ncomms10013/full/ncomms10013.html" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Perlman, E. J. et al. MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology wilms tumours. Nat. Commun. 6:10013 doi: 10.1038/ncomms10013 (2015).</a> This article is distributed by Nature Publishing Group, a division of Macmillan Publishers Limited under a Creative Commons Attribution 4.0 International License, as described at <a href="http://creativecommons.org/licenses/by/4.0/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">http://creativecommons.org/licenses/by/4.0/</a>. </p></div></div></div></div><div id="CDR0000062789__583"><h3>Bilateral Wilms Tumor</h3><p id="CDR0000062789__997">Approximately 5% to 10% of individuals with Wilms tumor have bilateral or multicentric tumors. The prevalence of bilateral involvement is higher in individuals with genetic predisposition syndromes than in those without predisposition syndromes. For example, in 545 cases of bilateral Wilms tumors, bona fide pathogenic germline variants were found in 22% of patients.[<a class="bk_pop" href="#CDR0000062789_rl_1_122">122</a>] The most common predisposition variants are mutations of <i>WT1</i> and 11p15 loss of imprinting.[<a class="bk_pop" href="#CDR0000062789_rl_1_21">21</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_71">71</a>]</p><p id="CDR0000062789__999">Bilateral Wilms tumor with <i>WT1</i> mutations are associated with early presentation in pediatric patients (age 10 months vs. age 39 months for those without a mutation) and a high frequency of <i>WT1</i> nonsense mutations in exon 8. Three percent of patients with bilateral Wilms tumor have affected family members.[<a class="bk_pop" href="#CDR0000062789_rl_1_123">123</a>]</p><p id="CDR0000062789__1978">Genomic analysis of kidney tissue in bilateral Wilms tumor indicates that a clonal expansion early in the nephrogenesis of normal-appearing but genetically aberrant precursor lesions occurred before the divergence of left and right kidney primordia.[<a class="bk_pop" href="#CDR0000062789_rl_1_61">61</a>]</p></div><div id="CDR0000062789__558"><h3>Screening Children Predisposed to Wilms Tumor</h3><p id="CDR0000062789__559">Children with a significant increased predisposition to develop Wilms tumor (e.g.,
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most children with Beckwith-Wiedemann syndrome or other overgrowth syndromes, WAGR syndrome, Denys-Drash syndrome, sporadic aniridia, or isolated hemihyperplasia) are usually screened with ultrasonography every 3
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months until they reach at least age 8 years.[<a class="bk_pop" href="#CDR0000062789_rl_1_84">84</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_124">124</a>] Early-stage, asymptomatic, small Wilms tumors may be discovered and potentially removed with renal-sparing surgery.[<a class="bk_pop" href="#CDR0000062789_rl_1_124">124</a>]</p><p id="CDR0000062789__675">Tumor screening programs for each overgrowth syndrome have been suggested. These programs were based on published age, incidence of tumor type, and recommendations from the 2016 American Association for Cancer Research (AACR) Childhood Cancer Predisposition Workshop. Although data about different cancer risks based on genetic or epigenetic subgroups for certain syndromes are emerging, and subgroup-specific recommendations have been developed in Europe, these practices have not been adopted in the United States. The AACR workshop committee proposed a uniform screening approach for all syndromes associated with a greater-than-1% risk of Wilms tumor. Additional screening for hepatoblastoma by serum alpha-fetoprotein (AFP) measurement and ultrasonography is also recommended for patients with Beckwith-Wiedemann syndrome, trisomy 18, and Simpson-Golabi-Behmel syndrome.[<a class="bk_pop" href="#CDR0000062789_rl_1_125">125</a>]</p><p id="CDR0000062789__1994">On the basis of a literature search of patients with Beckwith-Wiedemann spectrum and Wilms tumor where the age at diagnosis was compared against data collected through the Surveillance, Epidemiology, and End Results (SEER) program, screening patients with Beckwith-Wiedemann spectrum seems to significantly decrease the age and stage at the time of diagnosis in this population. Screening until age 7 years is effective in detecting close to 95% of all Wilms tumors in Beckwith-Wiedemann spectrum. Screening until age 30 months may also prove useful for patients with IC2 LoM, consistent with the recommendations for hepatoblastoma screening in this population.[<a class="bk_pop" href="#CDR0000062789_rl_1_126">126</a>]</p><ul id="CDR0000062789__1271"><li class="half_rhythm"><div class="half_rhythm"><b>Beckwith-Wiedemann syndrome.</b> Approximately 8% of patients with Beckwith-Wiedemann syndrome will develop a malignancy, with the most common being either Wilms tumor or hepatoblastoma, although adrenal tumors can also occur.[<a class="bk_pop" href="#CDR0000062789_rl_1_95">95</a>] </div><div class="half_rhythm"> Screening for hepatoblastoma or adrenal tumors with abdominal ultrasonography and serum AFP usually begins at birth or when the syndrome is diagnosed and continues until age 4 years. After age 4 years, most hepatoblastomas will have occurred, and imaging may be limited to renal ultrasonography, which is quicker and does not require fasting before the exam.[<a class="bk_pop" href="#CDR0000062789_rl_1_127">127</a>]</div><div class="half_rhythm"> Screening for Wilms tumor usually continues until age 7 years. Physical examination by a specialist (geneticist or pediatric oncologist) is recommended twice per year, and ongoing education regarding tumor manifestations, reinforcing the rationale for screening and compliance with the screening regimen, is discussed.[<a class="bk_pop" href="#CDR0000062789_rl_1_125">125</a>]</div><div class="half_rhythm">Proposed screening guidelines for Wilms tumor are available for patients with Beckwith-Wiedemann syndrome who have undergone molecular subtyping [<a class="bk_pop" href="#CDR0000062789_rl_1_95">95</a>] (refer to the <a href="#CDR0000062789__1203">Genomics of Wilms Tumor</a> section of this summary for more information about the molecular subtypes). The four main molecular subtypes of Beckwith-Wiedemann syndrome (ICR1-GoM, ICR2-LoM, UPD, and <i>CDKN1C</i> mutation) are characterized by specific genotype-phenotype correlations, including tumor risk.</div><div class="half_rhythm">Proposed screening for specific molecular subtypes of Beckwith-Wiedemann syndrome is as follows:<dl id="CDR0000062789__1274" class="temp-labeled-list"><dt>-</dt><dd><p class="no_top_margin">Patients with a defect of the ICR1 region (ICR1-GoM) and UPD should undergo abdominal ultrasonography every 3 months until age 8 to 10 years; a clinical examination of the abdomen and muscle mass occurs monthly for the first year and then at 3-month intervals, between ultrasonography scans, until age 6 years. </p></dd><dt>-</dt><dd><p class="no_top_margin">For patients with loss of imprinting at ICR2 (ICR2-LoM), an abdominal ultrasonography is performed at the time of clinical or molecular diagnosis; only patients with organomegaly or severe hemihyperplasia require surveillance by ultrasonography scans. Monthly clinical examinations are performed for the first 2 years, followed by clinical examinations every 3 to 6 months until age 6 years.</p></dd><dt>-</dt><dd><p class="no_top_margin">Patients with a <i>CDKN1C</i> mutation are not at high risk of developing Wilms tumor. There are no data to support routine screening.</p></dd></dl></div></li><li class="half_rhythm"><div class="half_rhythm"><b>Hemihyperplasia.</b> Children with hemihyperplasia are also at risk of developing liver tumors, adrenal tumors, and Wilms tumor (risk, 3%–4%). Screening with abdominal ultrasonography and serum AFP is suggested until age 4 years. After age 4 years, most hepatoblastomas will have occurred, and imaging may be limited to renal ultrasonography, which is quicker and does not require fasting before the exam.[<a class="bk_pop" href="#CDR0000062789_rl_1_125">125</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Sporadic aniridia.</b> Newborns born with sporadic aniridia should undergo molecular testing for deletion analysis of <i>PAX6</i> and <i>WT1</i>. If a deletion of <i>WT1</i> is observed, the child should be screened with ultrasonography every 3 months until age 8 years, and the parents should be educated about the need for early identification and treatment of Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_84">84</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_128">128</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_129">129</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Children of survivors of bilateral Wilms tumor.</b> Although the risk of Wilms tumor in the children of survivors of bilateral Wilms tumor is unknown and likely varies with the gene in which the mutation occurred, some experts recommend screening such children with serial ultrasonography examinations every 3 months until age 8 years.[<a class="bk_pop" href="#CDR0000062789_rl_1_69">69</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Bohring-Opitz syndrome.</b> Bohring-Opitz syndrome is a rare genetic condition associated with <i>ASXL1</i> mutations. Screening with abdominal ultrasonography every 3 to 4 months in the first 8 years of life has been suggested because of the 7% incidence of a renal neoplastic process in patients with Bohring-Opitz syndrome.[<a class="bk_pop" href="#CDR0000062789_rl_1_42">42</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Simpson-Golabi-Behmel syndrome.</b> Affected males with Simpson-Golabi-Behmel syndrome with <i>GPC3</i> mutations or deletions have an approximate 10% risk of Wilms tumor. Regular age-dependent screening for tumors, including abdominal ultrasonography, urinalysis, and biochemical markers, is recommended for males with Simpson-Golabi-Behmel syndrome, although the true benefit has not been determined. Carrier females are not at increased risk of Wilms tumor and do not require surveillance.[<a class="bk_pop" href="#CDR0000062789_rl_1_84">84</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Klippel-Trénaunay syndrome.</b> The risk of Wilms tumor in children with Klippel-Trénaunay syndrome (a unilateral limb overgrowth syndrome) was no different than the risk in the general population when assessed using the NWTS database. Routine ultrasonography surveillance is not recommended.[<a class="bk_pop" href="#CDR0000062789_rl_1_130">130</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Perlman syndrome.</b> Perlman syndrome is a rare congenital overgrowth syndrome that has an autosomal recessive inheritance pattern. A molecular diagnosis can be made by the presence of inactivating mutations in <i>DIS3L2</i> on chromosome 2q37.1. Fifty-three percent of children will die in the neonatal period. The kidneys show nephroblastomatosis in about 75% of cases. It is recommended that patients who survive the neonatal period be offered regular surveillance similar to that offered to patients with Beckwith-Wiedemann syndrome.[<a class="bk_pop" href="#CDR0000062789_rl_1_125">125</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>DICER1 syndrome.</b> Cystic nephroma is seen in 10% of families presenting with pleuropulmonary blastoma, typically occurring before age 4 years. Rare progression to anaplastic sarcoma of the kidney may occur. DICER1 syndrome includes an elevated risk of Wilms tumor, which is not a consequence of a prior cystic nephroma. Surveillance with abdominal ultrasonography, similar to Beckwith-Wiedemann syndrome, may be offered, but the age at which this should be stopped or reduced in frequency has not been established.[<a class="bk_pop" href="#CDR0000062789_rl_1_131">131</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_132">132</a>] Thirteen years is the oldest reported age of a Wilms tumor diagnosis in a <i>DICER1</i> mutation carrier.[<a class="bk_pop" href="#CDR0000062789_rl_1_108">108</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_133">133</a>]</div></li></ul><div id="CDR0000062789__1099"><h4>Genetic counseling</h4><p id="CDR0000062789__1100">The frequency of malformations observed in patients with Wilms tumor underlines the need for genetic counseling, molecular and genetic explorations, and follow-up. </p><p id="CDR0000062789__1114">A French study concluded that patients need to be referred for genetic counseling if they have one of the following:[<a class="bk_pop" href="#CDR0000062789_rl_1_8">8</a>]</p><ul id="CDR0000062789__1115"><li class="half_rhythm"><div>One major abnormality such as:<dl id="CDR0000062789__1116" class="temp-labeled-list"><dt>-</dt><dd><p class="no_top_margin">Beckwith-Wiedemann symptoms (macroglossia, neonatal or postnatal macrosomia, abdominal wall defects, or visceromegaly); or</p></dd></dl></div></li><li class="half_rhythm"><div>One condition such as:<dl id="CDR0000062789__1117" class="temp-labeled-list"><dt>-</dt><dd><p class="no_top_margin">Hemihyperplasia.</p></dd><dt>-</dt><dd><p class="no_top_margin">Overgrowth syndrome.</p></dd><dt>-</dt><dd><p class="no_top_margin">Mental retardation.</p></dd><dt>-</dt><dd><p class="no_top_margin">Aniridia.</p></dd><dt>-</dt><dd><p class="no_top_margin">Diffuse mesangial sclerosis.</p></dd></dl></div></li><li class="half_rhythm"><div>Two or more minor malformations such as:<dl id="CDR0000062789__1118" class="temp-labeled-list"><dt>-</dt><dd><p class="no_top_margin">Inguinal or umbilical hernia.</p></dd><dt>-</dt><dd><p class="no_top_margin">Hypospadias.</p></dd><dt>-</dt><dd><p class="no_top_margin">Renal abnormalities.</p></dd><dt>-</dt><dd><p class="no_top_margin">Ectopic testis.</p></dd></dl></div></li></ul><p id="CDR0000062789__1119">Simple oncological follow-up is indicated when there is no malformation or when there is only one minor malformation.[<a class="bk_pop" href="#CDR0000062789_rl_1_8">8</a>]</p><p id="CDR0000062789__1120">After genetic counseling occurs, testing for <i>WT1</i> mutations should be considered for patients who have the following:</p><ul id="CDR0000062789__1121"><li class="half_rhythm"><div>Bilateral Wilms tumor.</div></li><li class="half_rhythm"><div>Familial Wilms tumor.</div></li><li class="half_rhythm"><div>Wilms tumor and age younger than 6 months.</div></li><li class="half_rhythm"><div>Genitourinary abnormality.</div></li><li class="half_rhythm"><div>Mental retardation association.</div></li></ul><p id="CDR0000062789__1122">Testing for an 11p15 abnormality should be considered for patients exhibiting any symptoms of Beckwith-Wiedemann syndrome, hemihyperplasia, or bilateral or familial Wilms tumor.</p></div></div><div id="CDR0000062789__898"><h3>Clinical Features of Wilms Tumor</h3><p id="CDR0000062789__904">Most Wilms tumor patients present asymptomatically with an abdominal mass noticed by a parent or pediatrician on a well-child visit. In children with known predisposing clinical syndromes, renal tumors can be found during routine screening. Clinical findings may include the following:</p><ul id="CDR0000062789__905"><li class="half_rhythm"><div>A lump, swelling, or pain in the abdomen. Most children present with an asymptomatic mass that is noted when they are bathed or dressed. Abdominal pain is present in 40% of children.</div></li><li class="half_rhythm"><div>Blood in the urine. Gross hematuria occurs in about 18% of children with Wilms tumor at presentation, and microscopic hematuria is seen in 24% of patients.[<a class="bk_pop" href="#CDR0000062789_rl_1_134">134</a>]</div></li><li class="half_rhythm"><div>Hypertension. About 25% of children have hypertension at presentation, which is attributed to activation of the renin-angiotensin system.</div></li><li class="half_rhythm"><div>Hypercalcemia. Symptomatic hypercalcemia can sometimes be seen at presentation of rhabdoid tumors.</div></li><li class="half_rhythm"><div>Constitutional symptoms such as fever, anorexia, and weight loss occur in 10% of cases.</div></li></ul><p id="CDR0000062789__936">Children with Wilms tumor or other renal malignancies may also come to medical attention as a result of the following:</p><ul id="CDR0000062789__1068"><li class="half_rhythm"><div>Vascular obstruction or metastasis, including pulmonary symptoms caused by lung metastasis.</div></li><li class="half_rhythm"><div>Abdominal pain caused by liver metastasis, prominent abdominal wall vessels, or varicocele due to inferior vena cava obstruction.</div></li><li class="half_rhythm"><div>Pulmonary embolus (rare).</div></li></ul></div><div id="CDR0000062789__900"><h3>Diagnostic and Staging Evaluation for Wilms Tumor</h3><p id="CDR0000062789__901">Tests and procedures used to diagnose and stage Wilms tumor and other childhood kidney tumors include the following:</p><ol id="CDR0000062789__1004"><li class="half_rhythm"><div class="half_rhythm">Physical examination and history. Children with a renal mass are carefully assessed for signs of associated syndromes such as aniridia, developmental delay, hypospadias, cryptorchidism, pseudohermaphrodism, overgrowth, and hemihyperplasia.</div></li><li class="half_rhythm"><div class="half_rhythm">Complete blood
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count (CBC).</div></li><li class="half_rhythm"><div class="half_rhythm">Liver function test.</div></li><li class="half_rhythm"><div class="half_rhythm">Renal function test.</div></li><li class="half_rhythm"><div class="half_rhythm">Urinalysis.</div></li><li class="half_rhythm"><div class="half_rhythm">Abdominal imaging.<ul id="CDR0000062789__966"><li class="half_rhythm"><div>Abdominal x-ray.</div></li><li class="half_rhythm"><div>Ultrasonography exam of the abdomen. Ultrasonography exam of the abdomen is often performed before a more definitive computed tomography (CT) scan with contrast or magnetic resonance imaging (MRI) with contrast of the abdomen. This procedure is unnecessary after the definitive diagnostic study has been performed. </div></li><li class="half_rhythm"><div>CT scan with contrast or MRI of abdomen.[<a class="bk_pop" href="#CDR0000062789_rl_1_135">135</a>]<dl id="CDR0000062789__1232" class="temp-labeled-list"><dt>-</dt><dd><p class="no_top_margin">CT scan of the abdomen will confirm the renal origin of the mass and determine whether there are bilateral tumors.[<a class="bk_pop" href="#CDR0000062789_rl_1_136">136</a>] About 5% of renal masses thought to be Wilms tumor on the basis of clinical and radiological findings are diagnosed as another condition.[<a class="bk_pop" href="#CDR0000062789_rl_1_137">137</a>] </p></dd><dt>-</dt><dd><p class="no_top_margin">A review of children with bilateral Wilms tumor demonstrated that only 0.25% of bilateral tumors were missed with modern helical CT scans, all of which were small tumors.[<a class="bk_pop" href="#CDR0000062789_rl_1_138">138</a>]</p></dd><dt>-</dt><dd><p class="no_top_margin">Preoperative assessment by imaging of intravascular extension of Wilms tumor is essential to guide management. Four percent of Wilms tumor patients present with inferior vena cava or atrial involvement and 11% with renal vein involvement, which may lead to differences in management. Embolization of a caval thrombus to the pulmonary artery is rare but can be lethal, and the presence of a thrombus must be identified preoperatively to prevent this occurrence and guide treatment. A report from the COG shows that CT can accurately identify cavoatrial thrombus, obviating the need for ultrasonography if CT has already been performed.[<a class="bk_pop" href="#CDR0000062789_rl_1_139">139</a>]</p></dd><dt>-</dt><dd><p class="no_top_margin">Ascites beyond the cul-de-sac is most predictive of preoperative Wilms tumor rupture, regardless of attenuation. In the presence of ascites, fat stranding around the tumor and the presence of retroperitoneal fluid are highly predictive of rupture.[<a class="bk_pop" href="#CDR0000062789_rl_1_136">136</a>]</p></dd></dl></div></li></ul></div></li><li class="half_rhythm"><div class="half_rhythm">CT scan of chest. The common sites of metastases for Wilms tumor are the lung and liver. Approximately 15% of patients will present with pulmonary metastases. CT scanning provides the most sensitive method of detecting metastatic lung nodules.</div></li><li class="half_rhythm"><div class="half_rhythm">Chest x-ray is unnecessary if chest CT is performed initially.</div></li><li class="half_rhythm"><div class="half_rhythm">Fluorine F 18-fludeoxyglucose (18F-FDG) positron emission tomography (PET)-CT. Wilms tumor is 18F-FDG avid, and 18F-FDG PET-CT imaging adds clinically applicable information to conventional CT scan imaging. PET-CT may be particularly helpful in patients with bilateral disease or those receiving preoperative chemotherapy. 18F-FDG PET-CT highlights FDG-avid areas in the tumor and metastases, which corresponds to histologically confirmed active disease.[<a class="bk_pop" href="#CDR0000062789_rl_1_140">140</a>]</div></li><li class="half_rhythm"><div class="half_rhythm">von Willebrand disease work-up. About 1% to 8% of patients presenting with Wilms tumor have an acquired form of von Willebrand disease, although many are asymptomatic. von Willebrand multimers bind to Wilms tumor, reducing the plasma concentration to low levels.[<a class="bk_pop" href="#CDR0000062789_rl_1_141">141</a>] Some clinicians recommend evaluation for von Willebrand disease before surgery. </div></li><li class="half_rhythm"><div class="half_rhythm">Biopsy or resection. In children with a renal mass that clinically appears to be resectable or stage I or stage II Wilms tumor, a biopsy is not performed so that tumor cells are not spread during the biopsy. A biopsy would upstage such a patient to stage III. Nephrectomy (in North America) or chemotherapy (in Europe) is performed instead. Therefore, the diagnostic pathology is first seen when the nephrectomy specimen is examined.</div><div class="half_rhythm">Biopsy of a renal mass may be indicated if the mass is atypical by radiographic appearance for Wilms tumor, and the patient is not going to undergo immediate nephrectomy. If a primary nephrectomy cannot be performed, a biopsy, either open or with multiple cores, is required. The contraindications to primary nephrectomy are the following: <ul id="CDR0000062789__1928"><li class="half_rhythm"><div>Extension of tumor thrombus to the level of the hepatic veins. These patients should be considered for tumor resection after neoadjuvant chemotherapy when there is evidence of regression of the vena caval thrombus regardless of the degree of response of the primary tumor.</div></li><li class="half_rhythm"><div>The tumor involves contiguous structures whereby the only means of removing the kidney tumor requires removal of the other structure (e.g., spleen, pancreas, colon but excluding the adrenal gland and diaphragm). While Wilms tumors are frequently adherent to adjacent organs, in most cases, there is not frank invasion by the tumor and the organs can be dissected freely from the tumor. Radical en bloc resection (e.g., partial hepatectomy) is not generally warranted. If removal of a small section of diaphragm, psoas muscle, or tip of the pancreas allows the tumor to be removed intact, this is considered safe and appropriate.</div></li><li class="half_rhythm"><div>The surgeon's judgment that nephrectomy would result in significant or unnecessary morbidity/mortality, significant tumor spill, or residual tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_142">142</a>]</div></li><li class="half_rhythm"><div>If there is pulmonary compromise because of extensive pulmonary metastases or, in rare cases, hepatic disease.</div></li></ul></div><div class="half_rhythm">If a child undergoes a biopsy as the first procedure, they are considered stage III because they have gross residual tumors.</div><div class="half_rhythm">Biopsy tissue from inoperable Wilms tumor obtained before chemotherapy may be used for histologic review and initial treatment decisions. However, the use of biopsy to determine histology in an inoperable tumor remains controversial because biopsy may cause local tumor spread and the histologic classification of the Wilms tumor cannot be determined by biopsy.[<a class="bk_pop" href="#CDR0000062789_rl_1_142">142</a>]</div><div class="half_rhythm">Anaplastic histology can be difficult to detect in any biopsy sample because of tumor heterogeneity. Data from NWTS-4 and <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5 (COG-Q9401/NCT00002611)</a> demonstrated that, because of the histologic heterogeneity of Wilms tumor, a significant number of patients have anaplastic histology that is missed during an upfront biopsy whether it be a core needle biopsy or an incisional biopsy [<a class="bk_pop" href="#CDR0000062789_rl_1_143">143</a>] but revealed at the time of definitive surgery after chemotherapy.</div><div class="half_rhythm">Detection of a contralateral renal lesion in a child with Wilms tumor can change the stage and initial management of the patient, indicating a role for a renal-sparing approach without up-front surgery. The detection of contralateral renal lesions is important at baseline imaging because routine intraoperative exploration of the contralateral kidney is no longer recommended on the basis of the results of the NWTS-4 study.[<a class="bk_pop" href="#CDR0000062789_rl_1_135">135</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_138">138</a>] Treatment as a bilateral Wilms tumor should be considered if the initial imaging studies suggests a bilateral process. If the origin of the other lesion is indeterminate, a pathological assessment of that lesion should be considered before proceeding with a nephrectomy.[<a class="bk_pop" href="#CDR0000062789_rl_1_135">135</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_138">138</a>]</div><div class="half_rhythm">Children who have bilateral Wilms tumor are often treated without a biopsy.[<a class="bk_pop" href="#CDR0000062789_rl_1_144">144</a>] Biopsy can be avoided if the child is of typical age and the tumor has the usual radiographic appearance. This was assessed on the COG <a href="https://www.cancer.gov/clinicaltrials/NCT00945009" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0534 (NCT00945009)</a> study where 187 of 189 patients with Wilms tumor were treated initially without a biopsy. If after 6 weeks of therapy, response was less then 30% by RECIST1.1 criteria, bilateral biopsies were performed to assess for anaplasia, stromal differentiation, and rhabdomyomatous changes. If anaplasia was detected, the chemotherapy treatment was changed. If stromal differentiation or rhabdomyomatous changes were detected, further chemotherapy was unlikely to result in tumor shrinkage and definitive surgery was the suggested approach.[<a class="bk_pop" href="#CDR0000062789_rl_1_144">144</a>]</div></li></ol><p id="CDR0000062789__694">For patients with suspected Wilms tumor, additional preoperative staging studies are performed to assess lymph node status, intravascular extension, and rupture of Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_137">137</a>] </p><ul id="CDR0000062789__1002"><li class="half_rhythm"><div class="half_rhythm">Lymph node sampling is required to locally stage all Wilms tumor patients. Lymph nodes have shown to be of major prognostic value for both short-term and long-term survival. Gross inspection is notoriously inaccurate, with a false-negative rate of 31.3% and a false-positive rate of 18.1%.[<a class="bk_pop" href="#CDR0000062789_rl_1_145">145</a>]</div></li><li class="half_rhythm"><div class="half_rhythm">Intravascular extension of the Wilms tumor. Preoperative assessment of intravascular extension of Wilms tumor is essential to guide management. The presence of intravenous tumor thrombus in the lumen of the renal vein, inferior vena cava, and right atrium has been reported in up to 11.3% of Wilms tumor patients and may lead to differences in management. </div><div class="half_rhythm">In North America, local staging of Wilms tumor is performed with CT or MRI of the abdomen and pelvis. Contrast-enhanced CT for Wilms tumor patients has high sensitivity and specificity for detection of cavoatrial tumor thrombus that may impact surgical approach. Routine Doppler evaluation after CT has been performed but is not necessarily required.[<a class="bk_pop" href="#CDR0000062789_rl_1_139">139</a>] If the tumor is at or above the hepatic veins, a biopsy with preoperative chemotherapy is suggested because of the lower rate of serious intraoperative complications. Before surgical approach to the renal mass is performed, large tumor thrombi need to be controlled, especially when they extend above the hepatic vein, to avoid embolization of the tumor. In some cases, cardiopulmonary bypass is required.[<a class="bk_pop" href="#CDR0000062789_rl_1_146">146</a>]</div></li><li class="half_rhythm"><div class="half_rhythm">Wilms tumors can rupture before surgery. The term <i>rupture</i> is used to imply a break in the tumor capsule before surgery, whereas the term <i>spill</i> refers to a break in the tumor during surgery. Based on their similar diagnostic performances, either CT or MRI can be used to detect rupture. Although imaging findings of rupture have high specificity (88%), the diagnosis of rupture has to be confirmed at surgery. Imaging alone cannot be used for initial staging because of the low sensitivity and specificity for preoperative rupture and lymph node status.[<a class="bk_pop" href="#CDR0000062789_rl_1_147">147</a>]</div></li></ul></div><div id="CDR0000062789__551"><h3>Prognosis and Prognostic Factors for Wilms Tumor</h3><p id="CDR0000062789__552">Wilms tumor is a curable disease in most affected children.
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Since the 1980s, the 5-year survival rate for Wilms tumor with favorable histology (FH) has been consistently greater than 90%.[<a class="bk_pop" href="#CDR0000062789_rl_1_148">148</a>] This favorable outcome occurred with changes in therapy that included reductions in the length of therapy, dose of radiation, extent of fields irradiated, and the percentage of patients receiving radiation therapy.[<a class="bk_pop" href="#CDR0000062789_rl_1_149">149</a>]</p><p id="CDR0000062789__725">The prognosis for patients with Wilms tumor depends on the following:[<a class="bk_pop" href="#CDR0000062789_rl_1_150">150</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_153">153</a>]</p><ul id="CDR0000062789__726"><li class="half_rhythm"><div>Histopathologic features of the tumor (<a href="#CDR0000062789__587">FH</a> vs. <a href="#CDR0000062789__589">anaplastic histology</a>). (Refer to the <a href="#CDR0000062789__11">Histologic Findings in Wilms Tumor</a> section of this summary for more information.)</div></li><li class="half_rhythm"><div>Stage of disease at diagnosis.</div></li><li class="half_rhythm"><div>Molecular features of the tumor such as 1q gain and loss of heterozygosity of 1p and 16q. 1q gain, affecting 28% of Wilms tumors, is the most powerful predictor of outcome and is associated with an adverse outcome.[<a class="bk_pop" href="#CDR0000062789_rl_1_99">99</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_101">101</a>] (Refer to the <a href="#CDR0000062789__1203">Genomics of Wilms Tumor</a> section of this summary for more information.)</div></li><li class="half_rhythm"><div>Age. Older age is associated with an adverse prognosis.[<a class="bk_pop" href="#CDR0000062789_rl_1_154">154</a>]</div></li></ul></div><div id="CDR0000062789__968"><h3>Older Adolescents and Adults With Wilms Tumor</h3><p id="CDR0000062789__1900">Wilms tumor in patients older than 16 years is rare, with an incidence rate of less than 0.2 cases per 1 million per year.[<a class="bk_pop" href="#CDR0000062789_rl_1_155">155</a>] In Europe, the median age at diagnosis for adult patients with Wilms tumor (defined as age >15 years) is 34 years; however, patients older than 60 years have been reported.[<a class="bk_pop" href="#CDR0000062789_rl_1_155">155</a>] Three percent of Wilms tumors occur in adults. Wilms tumor represents less than 1% of all renal tumors in adults and may be an unexpected finding after nephrectomy for presumed renal cell carcinoma, which is the most common adult renal cancer.</p><p id="CDR0000062789__941">The outcomes for adolescent and young adult (AYA) patients (aged 15 to 39 years) and adult patients are inferior to the outcomes for children.</p><ul id="CDR0000062789__1958"><li class="half_rhythm"><div> In an analysis of patients with Wilms tumor in the Surveillance, Epidemiology, and End Results (SEER) database, AYA patients (n = 104) had a statistically worse 5-year OS rate (69% vs. 94%; <i>P</i> < .001) than did pediatric patients (n = 2,574).[<a class="bk_pop" href="#CDR0000062789_rl_1_156">156</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335138/" class="def">Level of evidence: 3iA</a>]</div></li></ul><p id="CDR0000062789__1959">The inferior outcome of the adult patients may be multifactorial, including differences in tumor biology between children and adults, incorrect diagnosis, inadequate staging (e.g., more likely to be staged as localized disease or to not receive lymph node sampling), undertreatment/poor compliance (e.g., not receiving radiation therapy), unfamiliarity of medical oncologists and pathologists with Wilms tumors in adults (possibly leading to diagnostic error and delay), delays in initiating the appropriate risk-adapted therapy, and lack of specific treatment protocols for adults.[<a class="bk_pop" href="#CDR0000062789_rl_1_157">157</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000561227/" class="def">Level of evidence: 3iii</a>]</p><div id="CDR0000062789__1961"><h4>Treatment of adults with Wilms tumor</h4><p id="CDR0000062789__1962"> Better results have been reported for adults when they are treated in pediatric trials. </p><p id="CDR0000062789__2016">The National Wilms Tumor Study (NWTS) Group reported the outcomes for adult patients with Wilms tumor from the NWTS-1, -2, and -3 trials.[<a class="bk_pop" href="#CDR0000062789_rl_1_158">158</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_160">160</a>] </p><ul id="CDR0000062789__2017"><li class="half_rhythm"><div>The 3-year OS rate for adults on the NWTS-1 trial was 24% (compared with 74% in children) and improved to a 5-year OS rate of 82.6% on the NWTS-3 trial, although the number of adult patients treated on each trial was 31 or fewer.</div></li><li class="half_rhythm"><div>These data suggest that many adults with Wilms tumor, if treated appropriately, can expect to be cured, especially if the tumor has not spread and/or is completely resected.</div></li></ul><p id="CDR0000062789__1963">For adults with refractory or recurrent disease, screening for potential therapeutic targets in the tumor should be considered.[<a class="bk_pop" href="#CDR0000062789_rl_1_161">161</a>]</p><p id="CDR0000062789__1901">The following recommendations from the renal tumor committees of the International Society of Pediatric Oncology (SIOP) and COG encourage a uniform approach to improve outcome for adults with Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_162">162</a>]</p><ul id="CDR0000062789__1902"><li class="half_rhythm"><div>Consult with a pediatric oncologist who has experience with the treatment of Wilms tumor as soon as a histological diagnosis is suspected.</div></li><li class="half_rhythm"><div>Avoid delaying the start of chemotherapy. Ideally, chemotherapy, and radiation therapy if necessary, should be started by day 14 postnephrectomy, although delaying the start until day 30 is acceptable.</div></li><li class="half_rhythm"><div>Be alert for toxicity of vincristine (neurotoxicity) and dactinomycin (hepatic toxicity) in adults.</div></li><li class="half_rhythm"><div>Register patients in pediatric renal tumor trials if studies are available and the patients are eligible.</div></li></ul></div></div><div id="CDR0000062789__11"><h3>Histologic Findings in Wilms Tumor</h3><p id="CDR0000062789__12">Although most patients with a histologic diagnosis of Wilms tumor do well
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with current treatment, approximately 10% of patients have histopathologic
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features that are associated with a worse prognosis, and in some types, with
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a high incidence of relapse and death. Wilms tumor can be separated into the following two
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prognostic groups on the basis of tumor and kidney histopathology:</p><ul id="CDR0000062789__734"><li class="half_rhythm"><div><a href="#CDR0000062789__587">Favorable histology (FH)</a>.</div></li><li class="half_rhythm"><div><a href="#CDR0000062789__589">Anaplastic histology</a>.</div></li></ul><div id="CDR0000062789__587"><h4>Favorable histology (FH)</h4><p id="CDR0000062789__588">Histologically, Wilms tumor mimics the triphasic development of a normal kidney
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consisting of blastemal, epithelial (tubules), and stromal cell types. Not all tumors are triphasic, and monophasic patterns may present diagnostic difficulties. </p><p id="CDR0000062789__1017">While associations between histologic features and prognosis or responsiveness to therapy have been suggested, with the exception of anaplasia, none of these features have reached statistical significance in North American treatment algorithms, and therefore, do not direct the initial therapy.[<a class="bk_pop" href="#CDR0000062789_rl_1_163">163</a>]</p></div><div id="CDR0000062789__589"><h4>Anaplastic histology</h4><p id="CDR0000062789__590">Anaplastic histology accounts for about 10% of Wilms tumor cases. Anaplastic histology is the single most important histologic predictor of response and survival in patients with Wilms tumor. Tumors occurring in older patients (aged 10–16 years) have a higher incidence of anaplastic histology.[<a class="bk_pop" href="#CDR0000062789_rl_1_164">164</a>] In bilateral tumors, 12% to 14% have been reported to have anaplastic histology in one kidney.[<a class="bk_pop" href="#CDR0000062789_rl_1_165">165</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_166">166</a>] </p><p id="CDR0000062789__1018">The following two histologic criteria must be present to confirm the diagnosis of anaplasia: </p><ul id="CDR0000062789__735"><li class="half_rhythm"><div>Presence of multipolar polyploid mitotic figures with marked nuclear enlargement.</div></li><li class="half_rhythm"><div>Hyperchromasia. </div></li></ul><p id="CDR0000062789__736">Changes on 17p consistent with mutations in the <i>TP53</i> gene have been associated with foci of anaplastic histology.[<a class="bk_pop" href="#CDR0000062789_rl_1_111">111</a>] Focal anaplasia is defined as the presence of one or more sharply localized regions of anaplasia in a primary tumor. All of these factors lend support to the hypothesis that anaplasia evolves as a late event from a subpopulation of Wilms tumor cells that have acquired additional genomic lesions.[<a class="bk_pop" href="#CDR0000062789_rl_1_167">167</a>] Focal anaplasia does not confer as poor a prognosis as does diffuse anaplasia.[<a class="bk_pop" href="#CDR0000062789_rl_1_152">152</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_168">168</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_169">169</a>]</p><p id="CDR0000062789__737">Anaplasia correlates best with responsiveness to therapy rather than to tumor aggressiveness. It is most consistently associated with poor prognosis when it is diffusely distributed and when
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identified at advanced stages. These tumors are more resistant to the chemotherapy traditionally used in children with FH Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_152">152</a>] </p></div><div id="CDR0000062789__591"><h4>Nephrogenic rests</h4><p id="CDR0000062789__592">Nephrogenic rests are abnormally retained embryonic kidney precursor cells arranged in clusters. Nephrogenic rests are found in about 1% of unselected pediatric autopsies, 35% of kidneys with unilateral Wilms tumor, and nearly 100% of kidneys with bilateral Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_170">170</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_171">171</a>]
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Preoperative chemotherapy does not appear to affect the overall prevalence of nephrogenic rests. Congenital anomalies have been reported in 12% of patients with nephrogenic rests, including in 9% of patients with unilateral Wilms tumor and in 33% of patients with bilateral disease.[<a class="bk_pop" href="#CDR0000062789_rl_1_7">7</a>]</p><p id="CDR0000062789__1019">The term <i>nephroblastomatosis</i> is defined as the presence of diffuse or multifocal nephrogenic rests. Nephrogenic rests can be subclassified according to the category of rest (intralobar or perilobar nephrogenic rests) and their growth phase (incipient or dormant nephrogenic rests, hyperplastic nephrogenic rests, and regressing or sclerosing nephrogenic rests). <i>Diffuse hyperplastic perilobar nephroblastomatosis</i> represents one unique category of nephroblastomatosis that forms a thick rind around one or both kidneys and is considered a preneoplastic condition. Distinguishing between Wilms tumor and diffuse hyperplastic perilobar nephrogenic rests may be a challenge, and it is critical to examine the juncture between the lesion and the surrounding renal parenchyma. Incisional biopsies are of no diagnostic value unless they include the margin between the lesion and the normal renal parenchyma.[<a class="bk_pop" href="#CDR0000062789_rl_1_172">172</a>] </p><p id="CDR0000062789__1020">The type and percentage of nephrogenic rests vary in patients with unilateral or bilateral disease. Patients with bilateral Wilms tumor have a higher proportion of perilobar rests (52%)
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than of intralobar or combined rests (32%) and higher relative proportions of rests, compared with patients with unilateral tumors (18% perilobar and 20% intralobar or both).[<a class="bk_pop" href="#CDR0000062789_rl_1_173">173</a>] Intralobar nephrogenic rests have been associated with stromal-type Wilms tumor and younger age at diagnosis.[<a class="bk_pop" href="#CDR0000062789_rl_1_7">7</a>]</p><p id="CDR0000062789__1000">Patients with any type of nephrogenic rest in a kidney removed for nephroblastoma are considered at increased risk for tumor formation in the remaining kidney. This risk decreases with patient age.[<a class="bk_pop" href="#CDR0000062789_rl_1_49">49</a>]</p><p id="CDR0000062789__1148">Bilateral diffuse hyperplastic perilobar nephroblastomatosis is generally treated with chemotherapy to reduce the risk of developing Wilms tumor. However, the risk of developing Wilms tumor remains high for patients who received chemotherapy (55% in one series) and for those who have been treated with chemotherapy for a prolonged period of time.[<a class="bk_pop" href="#CDR0000062789_rl_1_172">172</a>] If these patients develop Wilms tumor, they have a poorer prognosis than do other bilateral Wilms tumor patients, presumably because of the increased incidence of anaplasia in these cases (more than one-third of cases), and perhaps as a result of the development and selection of anaplasia in the surviving abnormal kidney cells.[<a class="bk_pop" href="#CDR0000062789_rl_1_172">172</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_174">174</a>]
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</p><p id="CDR0000062789__738">Extrarenal nephrogenic rests are rare and may develop into extrarenal Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_175">175</a>]</p></div></div><div id="CDR0000062789__23"><h3>Stage Information for Wilms Tumor</h3><p id="CDR0000062789__24"> Both the results of the imaging studies and the surgical and pathologic findings at nephrectomy are used to determine the stage of disease. The stage is the same for tumors with FH or anaplastic histology. Thus, the stage
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information is characterized by a statement of both criteria (for example, stage II,
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FH or stage II, anaplastic histology).[<a class="bk_pop" href="#CDR0000062789_rl_1_163">163</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_176">176</a>]</p><p id="CDR0000062789__25"> The staging system was originally developed by the NWTS Group and is still used by the COG. The staging system used in North America and incidence by stage are outlined below.[<a class="bk_pop" href="#CDR0000062789_rl_1_163">163</a>] Lymph node sampling is strongly recommended for all patients, even in the absence of clinically abnormal nodes, to achieve the most accurate stage.</p><div id="CDR0000062789__26"><h4>Stage I </h4><p id="CDR0000062789__160">In stage I Wilms tumor (43% of patients), all of the following criteria must be met: </p><ul id="CDR0000062789__161"><li class="half_rhythm"><div>Tumor is limited to the kidney and is completely resected.</div></li><li class="half_rhythm"><div>The renal capsule is intact.</div></li><li class="half_rhythm"><div>The tumor is not ruptured or biopsied before being removed.</div></li><li class="half_rhythm"><div>No involvement of renal sinus vessels.</div></li><li class="half_rhythm"><div>No evidence of the tumor at or beyond the margins of resection. </div></li><li class="half_rhythm"><div>All lymph nodes sampled are negative.</div></li></ul><p id="CDR0000062789__1233">For a tumor to qualify for certain therapeutic protocols such as very low-risk stage I, regional lymph nodes must be examined microscopically. </p></div><div id="CDR0000062789__28"><h4>Stage II </h4><p id="CDR0000062789__162"> In stage II Wilms tumor (20% of patients), the tumor is completely resected, and there is no evidence of tumor at or beyond the margins of resection. The tumor extends beyond the kidney as evidenced by any one of the following criteria: </p><ul id="CDR0000062789__165"><li class="half_rhythm"><div>There is regional extension of the tumor (i.e., penetration of the renal capsule, or extensive invasion of the soft tissue of the renal sinus, as discussed below).</div></li><li class="half_rhythm"><div>Blood vessels in the nephrectomy specimen outside the renal parenchyma, including those of the renal sinus, contain tumor cells. Margins are clear.</div></li><li class="half_rhythm"><div>Vascular extension of tumor is considered stage II only if it is completely removed en bloc in the nephrectomy specimen.</div></li></ul><p id="CDR0000062789__1143">All lymph nodes sampled are negative.</p><p id="CDR0000062789__1234">Rupture or spillage confined to the flank, including biopsy of the tumor, is now included in stage III by the COG Renal Tumor Committee (COG RTC); however, data to support this approach are controversial.[<a class="bk_pop" href="#CDR0000062789_rl_1_142">142</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_177">177</a>]</p></div><div id="CDR0000062789__33"><h4>Stage III </h4><p id="CDR0000062789__166">In stage III Wilms tumor (21% of patients), there is postsurgical residual nonhematogenous tumor that is confined to the abdomen. Any one of the following may occur: </p><ul id="CDR0000062789__167"><li class="half_rhythm"><div>Lymph nodes in the abdomen or pelvis are involved by tumor. (Lymph node involvement in the thorax or other extra-abdominal sites is a criterion for stage IV.)</div></li><li class="half_rhythm"><div>The tumor has penetrated through the peritoneal surface. </div></li><li class="half_rhythm"><div>Tumor implants are found on the peritoneal surface. </div></li><li class="half_rhythm"><div>Gross or microscopic tumor remains postoperatively (e.g., tumor cells are found at the margin of surgical resection on microscopic examination). </div></li><li class="half_rhythm"><div>The tumor is not completely resectable because of local infiltration into vital structures.</div></li><li class="half_rhythm"><div>Tumor rupture before surgery or any spill during surgery is considered stage III.</div></li><li class="half_rhythm"><div>Any biopsy is performed, regardless of type—Tru-cut biopsy, open biopsy, or fine-needle aspiration—before the tumor is removed.</div></li><li class="half_rhythm"><div>The tumor is removed in more than one piece (e.g., tumor cells are found in a separately excised adrenal gland; a tumor thrombus in the renal vein is removed separately from the nephrectomy specimen). Extension of the primary tumor in the vena cava into the thoracic vena cava and heart is considered stage III, rather than stage IV, even though outside the abdomen—and it can even be stage II if completely resected en bloc with the nephrectomy specimen.</div></li></ul><p id="CDR0000062789__923">Lymph node involvement and microscopic residual disease are reported as highly predictive of outcome in patients with stage III FH Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_178">178</a>]</p></div><div id="CDR0000062789__40"><h4>Stage IV </h4><p id="CDR0000062789__41"> In stage IV Wilms tumor (11% of patients), one of the following is present:</p><ul id="CDR0000062789__1275"><li class="half_rhythm"><div>Hematogenous metastases (lung, liver, bone, brain).</div></li><li class="half_rhythm"><div>Lymph node metastases outside the abdominopelvic region. </div></li></ul><p id="CDR0000062789__1276">The presence of tumor within the adrenal gland is not interpreted as metastasis and staging depends on all other staging parameters present. According to the criteria described above, the primary tumor is assigned a local stage, which determines local therapy. For example, a patient may have stage IV, local stage III disease.</p></div><div id="CDR0000062789__42"><h4>Stage V (bilateral)</h4><p id="CDR0000062789__43"> In stage V Wilms tumor (5% of patients), bilateral involvement by tumor is present at diagnosis. The current paradigm treats all patients with bilateral Wilms tumor the same for the first 6 or 12 weeks. After definitive surgery, the treatment is based on the highest stage of the remaining kidneys and the posttreatment pathology.[<a class="bk_pop" href="#CDR0000062789_rl_1_144">144</a>]</p></div></div><div id="CDR0000062789__386"><h3>Treatment of Wilms Tumor</h3><div id="CDR0000062789__48"><h4>Treatment option overview for Wilms tumor</h4><p id="CDR0000062789__49">Because of the relative rarity of Wilms tumor, all patients with this tumor
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should be considered for entry into a clinical trial. Treatment planning by a
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multidisciplinary team of cancer specialists (pediatric surgeon and/or pediatric
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urologist, pediatric radiation oncologist, and pediatric oncologist) who have
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experience treating children with Wilms tumor is necessary to determine and implement optimal
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treatment.
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</p><div id="CDR0000062789__1996"><h5>COG and SIOP approaches to Wilms tumor treatment</h5><p id="CDR0000062789__50">Most randomized clinical studies for treatment of children with Wilms tumor have been conducted by two large clinical groups (COG RTC and SIOP). Differences between the two groups affect staging and classification. There are two standard approaches to Wilms tumor treatment: the COG RTC uses immediate surgery for all unilateral tumors and the SIOP uses preoperative chemotherapy as the first step in treatment. Both groups use postoperative chemotherapy, except for selected cases who do not receive chemotherapy, and in advanced stages, radiation therapy is used in a risk-adapted approach. </p><ul id="CDR0000062789__790"><li class="half_rhythm"><div><b>COG RTC (includes the previous NWTS group):</b> The NWTS group established standard treatment for Wilms tumor in
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North America, consisting of initial nephrectomy (when feasible) followed by chemotherapy and, in some
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patients, radiation therapy.[<a class="bk_pop" href="#CDR0000062789_rl_1_179">179</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_181">181</a>] This approach allows for early and accurate histologic diagnosis, collection of biologic materials unaltered by therapy, and staging information, such as the presence of tumor spill or tumor involvement in lymph nodes, before chemotherapy is administered.</div></li><li class="half_rhythm"><div><b>SIOP:</b> SIOP is a European consortium whose trials provide preoperative chemotherapy before definitive resection for patients with renal tumors. This results in fewer tumor spills during surgery and lower postoperative stage.[<a class="bk_pop" href="#CDR0000062789_rl_1_182">182</a>] When the histological features of Wilms tumors from patients who underwent immediate surgery were compared with the histological features of patients who received preoperative chemotherapy, preoperative chemotherapy was shown to significantly alter the histology, with fewer blastemal and mixed histology types in the tumors. Additionally, there were fewer stage III tumors in the preoperative chemotherapy group.[<a class="bk_pop" href="#CDR0000062789_rl_1_183">183</a>]</div></li><li class="half_rhythm"><div>Both SIOP and COG treat infants younger than 6 months with a primary nephrectomy.[<a class="bk_pop" href="#CDR0000062789_rl_1_184">184</a>]</div></li></ul><p id="CDR0000062789__762">This summary focuses on the NWTS (now COG RTC) results and studies. </p><p id="CDR0000062789__1021">The major treatment and study conclusions of
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NWTS-1, NWTS-2, NWTS-3, NWTS-4, and <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5</a> are as follows:
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</p><ol id="CDR0000062789__116"><li class="half_rhythm"><div>Routine, postoperative radiation therapy of the flank is not necessary for
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children with stage I tumors or stage II tumors with FH
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when postnephrectomy combination chemotherapy consisting of vincristine and
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dactinomycin is administered.[<a class="bk_pop" href="#CDR0000062789_rl_1_181">181</a>]
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</div></li><li class="half_rhythm"><div> The prognosis for patients with stage III FH is best when treatment includes either
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(a) dactinomycin, vincristine, doxorubicin, and 10.8 Gy of radiation therapy to
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the flank; or (b) dactinomycin, vincristine, and 20 Gy of radiation therapy
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to the flank.
|
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Whole-abdominal radiation is indicated for extensive intraperitoneal disease or widespread intraperitoneal tumor spill with possible boost to gross residual disease.[<a class="bk_pop" href="#CDR0000062789_rl_1_181">181</a>]</div></li><li class="half_rhythm"><div> The addition of cyclophosphamide at the protocol dose (10 mg/kg/d for 3 days every 6 weeks) to the combination of vincristine,
|
|
dactinomycin, and doxorubicin does not improve prognosis for patients with
|
|
stage IV FH tumors.[<a class="bk_pop" href="#CDR0000062789_rl_1_181">181</a>]
|
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</div></li><li class="half_rhythm"><div>A single dose of dactinomycin per course (stages I–II FH,
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|
stage I anaplastic histology, stage III FH, stages III–IV, or stages
|
|
I–IV clear cell sarcoma of the kidney) is equivalent to the divided-dose
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|
courses, results in the same EFS, achieves greater dose intensity,
|
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and is associated with less toxicity and expense.[<a class="bk_pop" href="#CDR0000062789_rl_1_185">185</a>]
|
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</div></li><li class="half_rhythm"><div> Eighteen weeks of therapy is adequate for patients with stage I and stage II FH, and stage III and IV
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|
patients can be treated with 6 months of therapy instead of 15 months.[<a class="bk_pop" href="#CDR0000062789_rl_1_149">149</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_179">179</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_185">185</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_187">187</a>]
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</div></li><li class="half_rhythm"><div>Gain of 1q is associated with inferior survival in unilateral FH Wilms tumor. It is the single most powerful predictor of outcome, and in the presence of 1q gain, neither 1p nor 16q loss is significant. In the absence of 1q gain in unilateral FH Wilms tumor, 1p and/or 16q loss retain some prognostic significance and are associated with a higher risk of recurrence.[<a class="bk_pop" href="#CDR0000062789_rl_1_99">99</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_101">101</a>]</div></li></ol></div><div id="CDR0000062789__763"><h5>Surgery</h5><p id="CDR0000062789__764">The following operative principles have also evolved from NWTS (COG) trials: </p><ol id="CDR0000062789__791"><li class="half_rhythm"><div class="half_rhythm">The most important role
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for the surgeon is to ensure complete tumor removal without rupture and assess the extent of disease. Radical nephrectomy and lymph node
|
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sampling via a transabdominal or thoracoabdominal incision is the procedure
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|
of choice.[<a class="bk_pop" href="#CDR0000062789_rl_1_188">188</a>] A flank incision is not performed because it provides limited exposure to the kidney. </div><div class="half_rhythm">For patients with resectable tumors, preoperative biopsy or intraoperative biopsy is not performed because either would upstage the tumor in the current COG staging system.[<a class="bk_pop" href="#CDR0000062789_rl_1_188">188</a>]</div></li><li class="half_rhythm"><div class="half_rhythm">Routine exploration of the contralateral kidney is not necessary if technically adequate imaging studies do not suggest a bilateral process. If the initial imaging studies suggest bilateral kidney involvement, treatment approaches should facilitate renal-sparing surgery.[<a class="bk_pop" href="#CDR0000062789_rl_1_138">138</a>]</div></li><li class="half_rhythm"><div class="half_rhythm">About 2% of Wilms tumor cases have ureteral involvement. The presence of gross hematuria, nonfunctioning kidney, or hydronephrosis suggests the tumor may extend into the ureter, and cystoscopy is recommended. En bloc resection to avoid tumor spill is recommended.[<a class="bk_pop" href="#CDR0000062789_rl_1_189">189</a>]</div></li><li class="half_rhythm"><div class="half_rhythm">The surgeon needs to be aware of the risk of intraoperative spill, especially in patients who have right-sided and large tumors, as noted in a review of cases of intraoperative spill among 1,131 patients registered on COG study <a href="https://www.cancer.gov/clinicaltrials/NCT00898365" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN03B2</a> (<a href="https://clinicaltrials.gov/show/NCT00898365" title="Study NCT00898365" ref="pagearea=body&targetsite=external&targetcat=link&targettype=clinical-trial">NCT00898365</a>).[<a class="bk_pop" href="#CDR0000062789_rl_1_190">190</a>]</div></li><li class="half_rhythm"><div class="half_rhythm">Even if stage IV disease (e.g., pulmonary metastases) is evident on imaging, resection of the renal tumor should be considered. Treatment of local stage I or II Wilms tumor in the setting of distant metastasis does not require local radiation therapy.</div></li></ol><p id="CDR0000062789__765">Renal-sparing surgery remains controversial and is not supported by the data, except for children with the following:[<a class="bk_pop" href="#CDR0000062789_rl_1_191">191</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_192">192</a>]; [<a class="bk_pop" href="#CDR0000062789_rl_1_193">193</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335145/" class="def">Level of evidence: 3iiB</a>]</p><ul id="CDR0000062789__766"><li class="half_rhythm"><div>A solitary kidney.</div></li><li class="half_rhythm"><div>Predisposition to bilateral tumors. Some children who are predisposed to bilateral tumors and who have very small tumors detected by screening ultrasonography may be considered for renal-sparing surgery to preserve renal tissue.[<a class="bk_pop" href="#CDR0000062789_rl_1_191">191</a>] </div></li><li class="half_rhythm"><div>Horseshoe kidney. Wilms tumor arising in a horseshoe kidney is rare, and accurate preoperative diagnosis is important for planning the operative approach. Primary resection is possible in most cases. Inoperable cases can usually be resected after chemotherapy.[<a class="bk_pop" href="#CDR0000062789_rl_1_194">194</a>]</div></li><li class="half_rhythm"><div>Wilms tumor in infants with Denys-Drash or Frasier syndrome (to delay the need for dialysis). </div></li></ul><p id="CDR0000062789__767"> Renal-sparing surgery does not appear to be feasible for most patients at the time of diagnosis because of the location of the tumor within the kidney, even in patients with very low-risk tumors.[<a class="bk_pop" href="#CDR0000062789_rl_1_195">195</a>] In North America, renal-sparing surgery (partial nephrectomy) of unilateral Wilms tumor after administration of chemotherapy to shrink the tumor mass is considered investigational.[<a class="bk_pop" href="#CDR0000062789_rl_1_196">196</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_197">197</a>]</p><p id="CDR0000062789__768">Hilar and periaortic lymph node sampling is appropriate even if the nodes appear normal.[<a class="bk_pop" href="#CDR0000062789_rl_1_188">188</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_198">198</a>] Furthermore, any suspicious node basin is sampled. Margins of
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resection, residual tumor, and any suspicious node basins are marked with
|
|
titanium clips.
|
|
</p><p id="CDR0000062789__784">Wilms tumor rarely invades adjacent organs; therefore, resection of contiguous organs is seldom indicated. There is an increased incidence of complications occurring in more extensive resections that involve removal of additional organs beyond the diaphragm and adrenal gland. This finding has led to the recommendation in current COG protocols that patients in whom nephrectomy will require removal of additional organs should be considered for initial biopsy, neoadjuvant chemotherapy, and then secondary resection.[<a class="bk_pop" href="#CDR0000062789_rl_1_199">199</a>] Primary resection of liver metastasis is not recommended.[<a class="bk_pop" href="#CDR0000062789_rl_1_200">200</a>]</p></div><div id="CDR0000062789__769"><h5>Chemotherapy</h5><p id="CDR0000062789__770">Preoperative chemotherapy before nephrectomy is indicated in the following situations, which have been listed previously under situations requiring a biopsy (refer to the <a href="#CDR0000062789__900">Diagnostic and Staging Evaluation for Wilms Tumor</a> section of this summary for more information):[<a class="bk_pop" href="#CDR0000062789_rl_1_188">188</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_199">199</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_201">201</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_204">204</a>]</p><ul id="CDR0000062789__519"><li class="half_rhythm"><div>Wilms tumor in a solitary kidney.</div></li><li class="half_rhythm"><div>Synchronous bilateral Wilms tumor.</div></li><li class="half_rhythm"><div>Extension of tumor thrombus in the inferior vena cava above the level of the hepatic veins. About 4% of Wilms tumor patients present with inferior vena cava or atrial involvement, and 11% of patients present with renal vein involvement. Embolization of a caval thrombus to the pulmonary artery is rare but can be lethal, and the presence of a thrombus must be identified preoperatively to prevent this occurrence and guide treatment.[<a class="bk_pop" href="#CDR0000062789_rl_1_139">139</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_146">146</a>]</div></li><li class="half_rhythm"><div>Tumor involves contiguous structures whereby the only means of removing the kidney tumor requires removal of the other structures (e.g., spleen, pancreas, or colon but excluding the adrenal gland).</div></li><li class="half_rhythm"><div>Inoperable Wilms tumor.</div></li><li class="half_rhythm"><div>Pulmonary compromise resulting from extensive pulmonary metastases.</div></li></ul><p id="CDR0000062789__1022">Preoperative chemotherapy follows a biopsy. The biopsy may be
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performed through a flank approach.[<a class="bk_pop" href="#CDR0000062789_rl_1_146">146</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_205">205</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_209">209</a>] Adequate tissue is essential for accurate histological assessment and molecular studies. Preoperative chemotherapy includes doxorubicin in addition to vincristine and dactinomycin unless anaplastic histology is present; in such cases, chemotherapy then includes treatment with regimen I (refer to <a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__388/?report=objectonly" target="object" rid-figpopup="figCDR0000062789388" rid-ob="figobCDR0000062789388">Table 2</a>). The chemotherapy generally makes tumor
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removal easier by decreasing the size and vascular supply of the tumor; it may also reduce the frequency of surgical
|
|
complications.[<a class="bk_pop" href="#CDR0000062789_rl_1_142">142</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_146">146</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_199">199</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_201">201</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_210">210</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_211">211</a>]</p><p id="CDR0000062789__957">In North America, the use of preoperative chemotherapy in patients with evidence of a contained preoperative rupture has been suggested to avoid intraoperative spill, but this is controversial.[<a class="bk_pop" href="#CDR0000062789_rl_1_212">212</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_213">213</a>] The preoperative diagnosis of a contained retroperitoneal rupture on CT is difficult, even for experienced pediatric radiologists.[<a class="bk_pop" href="#CDR0000062789_rl_1_136">136</a>]</p><p id="CDR0000062789__772">All infants younger than 12 months (including newborns) who will be treated with chemotherapy require a 50% reduction in
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|
chemotherapy dose compared with the dose given to older children.[<a class="bk_pop" href="#CDR0000062789_rl_1_214">214</a>] Dosing for infants (younger than 12 months) is calculated per kilogram of weight, not body surface area. This reduction
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|
diminishes the toxic effects reported in children in this age group enrolled in
|
|
NWTS studies while maintaining an excellent overall outcome.[<a class="bk_pop" href="#CDR0000062789_rl_1_215">215</a>] </p><p id="CDR0000062789__792">Liver
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|
function tests in children with Wilms tumor are monitored closely during
|
|
the early course of therapy because hepatic toxic effects (sinusoidal obstructive syndrome, previously called veno-occlusive
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|
disease) have been reported in these patients.[<a class="bk_pop" href="#CDR0000062789_rl_1_216">216</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_217">217</a>] Dactinomycin or doxorubicin should not be
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|
administered during radiation therapy. Patients who develop renal failure while undergoing therapy can continue receiving chemotherapy with vincristine, dactinomycin, and doxorubicin. Vincristine and doxorubicin can be given at full doses; however, dactinomycin is associated with severe neutropenia. Reductions in dosing these agents may not be necessary, but accurate pharmacologic and pharmacokinetic studies are needed while the patient is receiving therapy.[<a class="bk_pop" href="#CDR0000062789_rl_1_218">218</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_219">219</a>]</p><p id="CDR0000062789__1925">Augmentation of therapy improves EFS for patients with FH Wilms tumor and loss of heterozygosity of 1p/16q. In the <a href="https://www.cancer.gov/clinicaltrials/NCT00352534" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0532 (NCT00352534)</a> and <a href="https://www.cancer.gov/clinicaltrials/NCT00379340" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0533 (NCT00379340)</a> trials, patients with stage I and stage II FH Wilms tumor who were treated with the DD-4A regimen (dactinomycin, vincristine, and doxorubicin) demonstrated a 4-year EFS rate of 87.3%, compared with the 4-year EFS rate of 68.8% (<i>P</i> = .042) for stage I and stage II patients treated on the <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5</a> trial. Patients with stage III and stage IV disease had a 4-year EFS rate of 90.2% when treated with regimen M (refer to <a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__388/?report=objectonly" target="object" rid-figpopup="figCDR0000062789388" rid-ob="figobCDR0000062789388">Table 2</a>), compared with a 61.3% 4-year EFS rate (<i>P</i> = .001) for stage III and stage IV patients treated on the NWTS-5 trial. Trends toward improved 4-year OS rates were seen in stage I and II patients and in stage III and IV patients.[<a class="bk_pop" href="#CDR0000062789_rl_1_220">220</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335153/" class="def">Level of evidence: 3iiiDi</a>]</p><p id="CDR0000062789__793">Postoperative radiation therapy to the tumor bed is required when a biopsy is performed or in the setting of local tumor stage III. In a study of 1,488 patients with Wilms tumors who underwent surgery and radiation therapy, delay in starting radiation therapy after surgery of greater than 14 days was associated with an increased risk of mortality for patients with nonmetastatic Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_221">221</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335150/" class="def">Level of evidence: 3iiiA</a>]</p><p id="CDR0000062789__794"><a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__388/?report=objectonly" target="object" rid-figpopup="figCDR0000062789388" rid-ob="figobCDR0000062789388">Table 2</a> describes the accepted chemotherapy regimens used to treat Wilms tumor.</p><div id="CDR0000062789__388" class="table"><h3><span class="title">Table 2. Accepted Chemotherapy Regimens for Wilms Tumor</span></h3><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK65842.23/table/CDR0000062789__388/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__CDR0000062789__388_lrgtbl__"><table class="no_top_margin"><thead><tr><th colspan="1" rowspan="1" style="vertical-align:top;">Regimen Name</th><th colspan="1" rowspan="1" style="vertical-align:top;">Regimen Description</th></tr></thead><tbody><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Regimen EE-4A [<a class="bk_pop" href="#CDR0000062789_rl_1_101">101</a>]</td><td colspan="1" rowspan="1" style="vertical-align:top;">Vincristine, dactinomycin × 18 weeks postnephrectomy</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Regimen DD-4A [<a class="bk_pop" href="#CDR0000062789_rl_1_101">101</a>]</td><td colspan="1" rowspan="1" style="vertical-align:top;">Vincristine, dactinomycin, doxorubicin × 24 weeks; baseline nephrectomy or biopsy with subsequent nephrectomy</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Regimen I [<a class="bk_pop" href="#CDR0000062789_rl_1_152">152</a>]</td><td colspan="1" rowspan="1" style="vertical-align:top;">Vincristine, doxorubicin, cyclophosphamide, etoposide × 24 weeks postnephrectomy</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Regimen M [<a class="bk_pop" href="#CDR0000062789_rl_1_222">222</a>]</td><td colspan="1" rowspan="1" style="vertical-align:top;">Vincristine, dactinomycin, doxorubicin, cyclophosphamide, and etoposide with subsequent radiation therapy</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Regimen UH1 [<a class="bk_pop" href="#CDR0000062789_rl_1_223">223</a>]</td><td colspan="1" rowspan="1" style="vertical-align:top;">Vincristine, doxorubicin, cyclophosphamide, carboplatin, and etoposide × 30 weeks + radiation therapy</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Regimen UH2 [<a class="bk_pop" href="#CDR0000062789_rl_1_223">223</a>]</td><td colspan="1" rowspan="1" style="vertical-align:top;">Vincristine, doxorubicin, cyclophosphamide, carboplatin, etoposide, vincristine, and irinotecan × 36 weeks + radiation therapy</td></tr></tbody></table></div></div></div><div id="CDR0000062789__1935"><h5>Radiation therapy</h5><p id="CDR0000062789__1936">Radiation therapy is used to improve local control and treat sites of metastatic disease. Radiation therapy has historically been dependent on stage and histology, but more recently is also guided by the tumor molecular signature.[<a class="bk_pop" href="#CDR0000062789_rl_1_224">224</a>]</p><div id="CDR0000062789__1997"><h5>COG approach</h5><p id="CDR0000062789__1938">Upfront surgery provides histologic confirmation and tumor extent, providing the rationale for adjuvant therapy, including radiation therapy. Besides histology, postoperative risk factors for worse local control include: (1) incomplete resection, (2) positive margins, and (3) nodal involvement. Radiation therapy is not used in patients with stage I or stage II FH Wilms tumor. For patients with FH stage III Wilms tumor, flank or abdominal radiation therapy is used for treatment. In cases of unfavorable histology (focal or diffuse anaplasia), flank or abdominal radiation therapy is indicated for all patients. (Refer to <a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__1948/?report=objectonly" target="object" rid-figpopup="figCDR00000627891948" rid-ob="figobCDR00000627891948">Table 3</a> for more information.)</p><p id="CDR0000062789__1998">Results of NWTS (COG RTS) trials have shown the following:</p><ul id="CDR0000062789__1939"><li class="half_rhythm"><div>Flank radiation therapy covers the tumor bed, involved nodal region, and entire adjacent vertebral bodies at 10.8 Gy in 1.8-Gy fractions. The dose of radiation therapy is based on the results of the NWTS-3 study in which there was no increase in abdominal relapse for stage III FH patients receiving 10 Gy versus 20 Gy with DD-4A chemotherapy.[<a class="bk_pop" href="#CDR0000062789_rl_1_225">225</a>]</div></li><li class="half_rhythm"><div>Whole-abdominal radiation therapy is 10.5 Gy in 1.5-Gy fractions and is used to treat diffuse spill or peritoneal metastasis.[<a class="bk_pop" href="#CDR0000062789_rl_1_220">220</a>]</div></li><li class="half_rhythm"><div>In the closed COG <a href="https://www.cancer.gov/clinicaltrials/NCT00335556" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0321 (NCT00335556)</a> study, the radiation therapy dose to the tumor bed was 10.8 Gy in 1.8-Gy fractions, with the exception of patients with stage III diffuse anaplasia, where a dose of 19.8 Gy in 1.8-Gy fractions was used. This remains the current standard of treatment.[<a class="bk_pop" href="#CDR0000062789_rl_1_223">223</a>]</div></li><li class="half_rhythm"><div>Results of the early NWTS studies (1 and 2) suggested that a radiation therapy delay of more than 10 days after surgery resulted in worse local control, particularly in unfavorable histology Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_226">226</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_227">227</a>] However, no difference in local control was found if radiation therapy was delayed more than 10 days after surgery for patients with stages II to IV FH tumors treated on the NWTS-3 or NWTS-4 trials.[<a class="bk_pop" href="#CDR0000062789_rl_1_95">95</a>] More recent data from the National Cancer Database confirmed improved survival in patients with nonmetastatic Wilms tumor who received adjuvant radiation therapy less than or equal to 14 days postoperatively.[<a class="bk_pop" href="#CDR0000062789_rl_1_221">221</a>] </div></li><li class="half_rhythm"><div>Results from the NWTS-3 and NWTS-4 trials indicated that there was no survival benefit of whole-lung irradiation in the setting of lung metastases seen on CT scan only.[<a class="bk_pop" href="#CDR0000062789_rl_1_228">228</a>] Current COG guidelines allow for omission of whole-lung irradiation in cases of FH disease without extrapulmonary metastases, loss of heterozygosity at 1p and 16q, and complete response at 6 weeks after vincristine, dactinomycin, and doxorubicin.[<a class="bk_pop" href="#CDR0000062789_rl_1_224">224</a>] When whole-lung irradiation is given, a dose of 12 Gy in 1.5-Gy fractions is indicated for children older than 12 months and 10.5 Gy in 1.5-Gy fractions for patients younger than 12 months with pulmonary metastasis.</div></li><li class="half_rhythm"><div>Other sites of metastatic disease in Wilms tumor are uncommon and may include liver, extra-abdominal nodes, brain, and bone. In the COG <a href="https://www.cancer.gov/clinicaltrials/NCT00379340" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0533 (NCT00379340)</a> study, the radiation therapy doses being used for patients younger than 16 years are 19.8 Gy in 1.8-Gy fractions to liver and gross residual nodes, 21.6 Gy in 1.8-Gy fractions to the whole brain with a boost of 10.8 Gy in 1.8-Gy fractions to gross metastatic disease in the brain, and 25.2 Gy in 14 fractions for bone metastasis. For patients older than 16 years, the radiation therapy dose to the whole brain and bone is increased to 30.6 Gy in 1.8-Gy fractions.</div></li></ul><div id="CDR0000062789__1948" class="table"><h3><span class="title">Table 3. Radiation Therapy Regimens used in Children’s Oncology Group AREN0532, AREN0533, and AREN0321 Protocols</span></h3><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK65842.23/table/CDR0000062789__1948/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__CDR0000062789__1948_lrgtbl__"><table class="no_margin"><thead><tr><th colspan="5" rowspan="1" style="text-align:center;vertical-align:top;">Local/Locoregional Disease</th></tr></thead><tbody><tr><td colspan="1" rowspan="1" style="vertical-align:top;"></td><td colspan="1" rowspan="1" style="vertical-align:top;"><b>Stage I</b></td><td colspan="1" rowspan="1" style="vertical-align:top;"><b>Stage II</b></td><td colspan="1" rowspan="1" style="vertical-align:top;"><b>Stage III</b></td><td colspan="1" rowspan="1" style="vertical-align:top;"><b>Stage III
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(diffuse spill, peritoneal metastasis, preoperative rupture)<sup>a</sup></b>
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</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Favorable histology</td><td colspan="1" rowspan="1" style="vertical-align:top;">No XRT </td><td colspan="1" rowspan="1" style="vertical-align:top;">No XRT</td><td colspan="1" rowspan="1" style="vertical-align:top;">10.8 Gy</td><td colspan="1" rowspan="1" style="vertical-align:top;">10.5 Gy</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Focal anaplasia</td><td colspan="1" rowspan="1" style="vertical-align:top;">10.8 Gy</td><td colspan="1" rowspan="1" style="vertical-align:top;">10.8 Gy</td><td colspan="1" rowspan="1" style="vertical-align:top;">10.8 Gy</td><td colspan="1" rowspan="1" style="vertical-align:top;">10.5 Gy</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Diffuse anaplasia</td><td colspan="1" rowspan="1" style="vertical-align:top;">10.8 Gy</td><td colspan="1" rowspan="1" style="vertical-align:top;">10.8 Gy</td><td colspan="1" rowspan="1" style="vertical-align:top;">19.8 Gy</td><td colspan="1" rowspan="1" style="vertical-align:top;">10.5 Gy + 9 Gy boost</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;"></td><td colspan="4" rowspan="1" style="text-align:center;vertical-align:top;"><b>Metastatic Disease</b></td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;"></td><td colspan="1" rowspan="1" style="vertical-align:top;"><b>Stage IV
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Lung</b>
|
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</td><td colspan="1" rowspan="1" style="vertical-align:top;"><b>Stage IV
|
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Liver
|
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</b></td><td colspan="1" rowspan="1" style="vertical-align:top;"><b>Stage IV
|
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Brain
|
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</b></td><td colspan="1" rowspan="1" style="vertical-align:top;"><b>Stage IV
|
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Bone
|
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</b></td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Favorable histology</td><td colspan="1" rowspan="1" style="vertical-align:top;">10.5 Gy for age <12 months<sup>b,c</sup>;
|
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12 Gy for age >12 months<sup>b,c</sup>
|
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</td><td colspan="1" rowspan="1" style="vertical-align:top;">19.8 Gy +/- 5.4 to 10.8 Gy boost<sup>d</sup></td><td colspan="1" rowspan="1" style="vertical-align:top;">21.6 Gy + 10.8 Gy boost for age <16 years;
|
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30.6 Gy for age >16 years
|
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</td><td colspan="1" rowspan="1" style="vertical-align:top;">25.2 Gy for age <16 years;
|
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30.6 Gy for age >16 years
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</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Focal or diffuse anaplasia</td><td colspan="1" rowspan="1" style="vertical-align:top;">10.5 Gy for age <12 months<sup>b</sup>;
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12 Gy for age >12 months<sup>b</sup>
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</td><td colspan="1" rowspan="1" style="vertical-align:top;">19.8 Gy +/- 5.4 to 10.8 Gy boost<sup>d</sup></td><td colspan="1" rowspan="1" style="vertical-align:top;">21.6 Gy + 10.8 Gy boost for age <16 years;
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30.6 Gy for age >16 years
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</td><td colspan="1" rowspan="1" style="vertical-align:top;">25.2 Gy for age <16 years;
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30.6 Gy for age >16 years
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</td></tr></tbody></table></div><div><div><dl class="temp-labeled-list small"><dt></dt><dd><div><p class="no_margin">XRT = radiation therapy.</p></div></dd><dt></dt><dd><div><p class="no_margin"><sup>a</sup>Requires whole-abdominal XRT in 1.5 Gy daily fractions. Patients with diffuse unresectable peritoneal implants receive 21 Gy.</p></div></dd><dt></dt><dd><div><p class="no_margin"><sup>b</sup>Whole-lung irradiation is given in 1.5 Gy daily fractions.</p></div></dd><dt></dt><dd><div><p class="no_margin"><sup>c</sup>Not all patients receive radiation therapy.</p></div></dd><dt></dt><dd><div><p class="no_margin"><sup>d</sup>A boost is given for macroscopic disease.</p></div></dd></dl></div></div></div></div><div id="CDR0000062789__1999"><h5>SIOP approach</h5><p id="CDR0000062789__1940">Based on the experience of previous SIOP trials, children who need radiation therapy undergo postoperative treatment to the flank and/or metastatic sites. The SIOP 1 to 9 trials demonstrated that preoperative radiation therapy or preoperative chemotherapy decreased the proportion of patients who developed tumor spillage, from more than 20% to 5%. The noninferiority of preoperative chemotherapy to preoperative radiation therapy in the SIOP 5 trial, and the concern over secondary malignancies with preoperative radiation therapy, led SIOP to recommend preoperative chemotherapy as the standard initial treatment.[<a class="bk_pop" href="#CDR0000062789_rl_1_182">182</a>] Over time, the percentage of children who were treated with postoperative radiation therapy decreased, from more than 90% to 15% and 25% in SIOP trials 6 to 9, SIOP 93-01, and SIOP-2001, respectively.[<a class="bk_pop" href="#CDR0000062789_rl_1_180">180</a>]</p></div></div></div><div id="CDR0000062789__973"><h4>Treatment of stage I Wilms tumor</h4><p id="CDR0000062789__974">
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<a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__951/?report=objectonly" target="object" rid-figpopup="figCDR0000062789951" rid-ob="figobCDR0000062789951">Table 4</a> provides an overview of the standard treatment options and survival data for patients with <a href="#CDR0000062789__26">stage I Wilms tumor</a>, based on published results. </p><div id="CDR0000062789__951" class="table"><h3><span class="title">Table 4. Overview of Standard Treatment Options for Stage I Wilms Tumor<sup>a</sup></span></h3><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK65842.23/table/CDR0000062789__951/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__CDR0000062789__951_lrgtbl__"><table class="no_margin"><thead><tr><th colspan="1" rowspan="1" style="vertical-align:top;">Histology</th><th colspan="1" rowspan="1" style="vertical-align:top;">4-Year RFS or EFS</th><th colspan="1" rowspan="1" style="vertical-align:top;">4-Year OS</th><th colspan="1" rowspan="1" style="vertical-align:top;">Treatment (refer to <a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__388/?report=objectonly" target="object" rid-figpopup="figCDR0000062789388" rid-ob="figobCDR0000062789388">Table 2</a> for chemotherapy regimen descriptions)</th></tr></thead><tbody><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FH <24 mo/tumor weight <550g</td><td colspan="1" rowspan="1" style="vertical-align:top;">90%</td><td colspan="1" rowspan="1" style="vertical-align:top;">100%</td><td colspan="1" rowspan="1" style="vertical-align:top;">Surgery, including lymph node biopsy only</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FH >24 mo/tumor weight >550g</td><td colspan="1" rowspan="1" style="vertical-align:top;">94% RFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">98%</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling followed by regimen EE-4A </td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FH with LOH 1p/16q (n = 8)</td><td colspan="1" rowspan="1" style="vertical-align:top;">100% EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">100%</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling followed by regimen DD-4A</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FA</td><td colspan="1" rowspan="1" style="vertical-align:top;">100%</td><td colspan="1" rowspan="1" style="vertical-align:top;">100% (n = 8)</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling followed by regimen DD-4A and XRT</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">DA </td><td colspan="1" rowspan="1" style="vertical-align:top;">100%<sup>b</sup></td><td colspan="1" rowspan="1" style="vertical-align:top;"> 100% (n = 10)</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling followed by regimen DD-4A and XRT </td></tr></tbody></table></div><div><div><dl class="temp-labeled-list small"><dt></dt><dd><div><p class="no_margin">DA = diffuse anaplastic; EFS = event-free survival; FA = focal anaplastic; FH = favorable histology; LOH = loss of heterozygosity; OS = overall survival; RFS = relapse-free survival; XRT = radiation therapy.</p></div></dd><dt></dt><dd><div><p class="no_margin"><sup>a</sup>Source: Grundy et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_101">101</a>] Shamberger et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_153">153</a>] Fernandez et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_224">224</a>] Dix et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_220">220</a>] and Daw et al.[<a class="bk_pop" href="#CDR0000062789_rl_1_229">229</a>]</p></div></dd><dt></dt><dd><div><p class="no_margin"><sup>b</sup>One patient with a pulmonary relapse 4.12 years after diagnosis.</p></div></dd></dl></div></div></div><p id="CDR0000062789__976">Evidence (surgery only for children younger than 2 years at diagnosis with stage I FH tumor that weighed <550 g):</p><p id="CDR0000062789__975">In the <a href="https://www.cancer.gov/clinicaltrials/NCT00352534" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0532 (NCT00352534)</a> trial, the COG validated the findings from the <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5</a> trial that nephrectomy only is appropriate therapy for patients younger than 2 years at diagnosis with stage I FH Wilms tumor that weighed less than 550 g.</p><ol id="CDR0000062789__977"><li class="half_rhythm"><div>The <a href="https://www.cancer.gov/clinicaltrials/NCT00352534" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0532 (NCT00352534)</a> trial was designed to confirm the findings from NWTS-5 that adjuvant chemotherapy could be omitted for children younger than 2 years at diagnosis with stage I FH Wilms tumor that weighed less than 550 g. A total of 116 patients met the criteria for very low-risk Wilms tumor and were enrolled on the study.[<a class="bk_pop" href="#CDR0000062789_rl_1_153">153</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_224">224</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_230">230</a>]<ul id="CDR0000062789__1306"><li class="half_rhythm"><div>Twelve patients relapsed.</div></li><li class="half_rhythm"><div>The estimated 4-year EFS rate was 89.7%, and the OS rate was 100%.</div></li><li class="half_rhythm"><div>11p15 methylation status was associated with relapse (20% relapse with loss of heterozygosity, 25% relapse with loss of imprinting, and 3.3% relapse with retention of the normal imprinting [<i>P</i> = .011]).</div></li><li class="half_rhythm"><div>Risk of developing metachronous Wilms tumor is very low in patients with very low-risk Wilms tumor who lack evidence of an underlying syndrome.</div></li></ul></div></li></ol><p id="CDR0000062789__2000">Evidence (treatment of stage I epithelial-predominant favorable-histology Wilms tumor):</p><ol id="CDR0000062789__2001"><li class="half_rhythm"><div>The COG reported the outcomes for patients of all ages with stage I FH Wilms tumors showing epithelial-predominant histology. Approximately 20% of stage I FH Wilms tumors registered on AREN03B2 were epithelial predominant. In this group of 177 patients with stage I epithelial-predominant FH Wilms tumors, 117 patients were treated with EE4A, and 57 patients were classified as having a very low-risk Wilms tumor and were treated with observation only.[<a class="bk_pop" href="#CDR0000062789_rl_1_231">231</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335150/" class="def">Level of evidence: 3iiiA</a>]<ul id="CDR0000062789__1968"><li class="half_rhythm"><div>The 4-year EFS rate was 96.2%, and the OS rate was 100%.</div></li><li class="half_rhythm"><div>There was no statistical difference in EFS and OS based on age at diagnosis (<48 months and >48 months) or treatment (EE4A vs. observation only).</div></li><li class="half_rhythm"><div>There were six events: three patients developed contralateral tumors after their initial diagnosis, and two of these patients had received adjuvant chemotherapy for their initial tumors. Three patients developed metastatic disease, and all of these patients had previously received EE4A as their primary therapy.</div></li></ul></div></li></ol><p id="CDR0000062789__2002">Evidence (treatment of anaplastic stage I Wilms tumor):</p><ol id="CDR0000062789__2003"><li class="half_rhythm"><div>The <a href="https://www.cancer.gov/clinicaltrials/NCT00335556" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0321 (NCT00335556)</a> study demonstrated that outcomes for patients with stage I anaplastic Wilms tumor were improved with the addition of doxorubicin and flank radiation therapy to vincristine/dactinomycin therapy.[<a class="bk_pop" href="#CDR0000062789_rl_1_229">229</a>]<ul id="CDR0000062789__1943"><li class="half_rhythm"><div>Four-year EFS and OS rate estimates were 100% in AREN0321, compared with 70% and 81.5%, respectively, in an updated analysis of 27 patients from <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5</a> (median follow up, 13.3 years). One patient with diffuse anaplasia relapsed 4.12 years after diagnosis on the AREN0321 trial.</div></li><li class="half_rhythm"><div>The addition of doxorubicin and radiation therapy to AREN0321 was on the basis of the pattern of relapse observed in stage I anaplastic Wilms tumor in the abdomen and distant sites in the NWTS-5 trial.</div></li><li class="half_rhythm"><div>Retrospective analysis of all patients with stage I anaplastic Wilms tumor treated on NWTS-1 through NWTS-5 and AREN0321 showed a significant improvement in EFS for patients treated with doxorubicin (4-year EFS rate, 97.2% vs. 77.5%; <i>P</i> = .01), but no difference in EFS according to flank radiation therapy was shown (4-year EFS rate, 91.7% vs. 80.2%; <i>P</i> = .15).</div></li><li class="half_rhythm"><div>The rate of local recurrence was low (3.6%) and appeared to be similar for patients who received flank radiation therapy (4%) and patients who did not receive flank radiation therapy (6.2%). Local relapse occurred only in patients with diffuse anaplasia.</div></li></ul></div></li></ol><div id="CDR0000062789__TrialSearch_973_sid_3"><h5>Current Clinical Trials</h5><p id="CDR0000062789__TrialSearch_973_22">Use our <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/advanced-search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">advanced clinical trial search</a> to find NCI-supported cancer clinical trials that are now enrolling patients. The search can be narrowed by location of the trial, type of treatment, name of the drug, and other criteria. <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">General information</a> about clinical trials is also available.</p></div></div><div id="CDR0000062789__978"><h4>Treatment of stage II Wilms tumor</h4><p id="CDR0000062789__979"><a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__931/?report=objectonly" target="object" rid-figpopup="figCDR0000062789931" rid-ob="figobCDR0000062789931"> Table 5</a> provides an overview of the standard treatment options and survival data for patients with <a href="#CDR0000062789__28">stage II Wilms tumor</a>, based on published results.</p><div id="CDR0000062789__931" class="table"><h3><span class="title">Table 5. Overview of Standard Treatment Options for Stage II Wilms Tumor<sup>a</sup></span></h3><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK65842.23/table/CDR0000062789__931/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__CDR0000062789__931_lrgtbl__"><table class="no_margin"><thead><tr><th colspan="1" rowspan="1" style="vertical-align:top;">Histology</th><th colspan="1" rowspan="1" style="vertical-align:top;">4-Year RFS or EFS</th><th colspan="1" rowspan="1" style="vertical-align:top;">4-Year OS</th><th colspan="1" rowspan="1" style="vertical-align:top;">Treatment (refer to <a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__388/?report=objectonly" target="object" rid-figpopup="figCDR0000062789388" rid-ob="figobCDR0000062789388">Table 2</a> for chemotherapy regimen descriptions)</th></tr></thead><tbody><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FH</td><td colspan="1" rowspan="1" style="vertical-align:top;">86% RFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">98%</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling followed by regimen EE-4A</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FH LOH 1p/16q (n = 24)</td><td colspan="1" rowspan="1" style="vertical-align:top;">83% EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">100%</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling followed by regimen DD-4A</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FA </td><td colspan="1" rowspan="1" style="vertical-align:top;">80% EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">80% (n = 5)</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling followed by abdominal XRT and regimen DD-4A</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">DA</td><td colspan="1" rowspan="1" style="vertical-align:top;">84% EFS </td><td colspan="1" rowspan="1" style="vertical-align:top;">84% (n = 19)</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling followed by abdominal XRT and regimen UH1</td></tr></tbody></table></div><div><div><dl class="temp-labeled-list small"><dt></dt><dd><div><p class="no_margin">DA = diffuse anaplastic; EFS = event-free survival; FA = focal anaplastic; FH = favorable histology; LOH = loss of heterozygosity; OS = overall survival; RFS = relapse-free survival; XRT = radiation therapy.</p></div></dd><dt></dt><dd><div><p class="no_margin"><sup>a</sup>Source: Grundy et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_101">101</a>] Dome et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_152">152</a>] Dix et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_220">220</a>] and Daw et al.[<a class="bk_pop" href="#CDR0000062789_rl_1_223">223</a>]</p></div></dd></dl></div></div></div><div id="CDR0000062789__2004"><h5>Treatment of stage II patients with intraoperative spill</h5><p id="CDR0000062789__981">In a review of 499 patients from NWTS-4 with stage II FH Wilms tumor, 95 of the patients experienced tumor spill. The 8-year RFS and OS rates for patients who experienced intraoperative tumor spill and were treated with vincristine and dactinomycin without flank radiation therapy were lower, at 75.7% and 90.3%, than the 85% and 95.6% rates for those who did not experience tumor spill. None of these differences achieved statistical significance.[<a class="bk_pop" href="#CDR0000062789_rl_1_177">177</a>]</p><p id="CDR0000062789__980">On NWTS-3, NWTS-4, and <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5</a>, patients with intraoperative spill were divided into two groups: (1) those with diffuse spillage involving the whole abdominal cavity; and (2) those with local spillage confined to the flank. Patients with diffuse spillage were treated with radiation therapy to the entire abdomen and three-drug chemotherapy (vincristine, dactinomycin, and doxorubicin), whereas patients with local spillage were treated with vincristine and dactinomycin only. On the basis of an analysis of patients treated on NWTS-3 and NWTS-4 indicating that patients with stage II disease and local spillage had inferior OS compared with patients with stage II disease without local spillage, COG studies treat patients with local spillage with doxorubicin and flank radiation.[<a class="bk_pop" href="#CDR0000062789_rl_1_232">232</a>] This approach is controversial and has not been tested; therefore, it should not be considered standard. </p></div><div id="CDR0000062789__TrialSearch_978_sid_4"><h5>Current Clinical Trials</h5><p id="CDR0000062789__TrialSearch_978_22">Use our <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/advanced-search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">advanced clinical trial search</a> to find NCI-supported cancer clinical trials that are now enrolling patients. The search can be narrowed by location of the trial, type of treatment, name of the drug, and other criteria. <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">General information</a> about clinical trials is also available.</p></div></div><div id="CDR0000062789__982"><h4>Treatment of stage III Wilms tumor</h4><p id="CDR0000062789__983">
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<a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__932/?report=objectonly" target="object" rid-figpopup="figCDR0000062789932" rid-ob="figobCDR0000062789932">Table 6</a> provides an overview of the standard treatment options and survival data for patients with <a href="#CDR0000062789__33">stage III Wilms tumor</a>, based on published results. </p><p id="CDR0000062789__985">For patients classified as stage III purely on the basis of local spill, refer to the <a href="#CDR0000062789__978">Treatment of stage II Wilms tumor</a> section of this summary.</p><div id="CDR0000062789__932" class="table"><h3><span class="title">Table 6. Overview of Standard Treatment Options for Stage III Wilms Tumor<sup>a</sup></span></h3><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK65842.23/table/CDR0000062789__932/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__CDR0000062789__932_lrgtbl__"><table class="no_margin"><thead><tr><th colspan="1" rowspan="1" style="vertical-align:top;">Histology</th><th colspan="1" rowspan="1" style="vertical-align:top;">4-Year RFS or EFS</th><th colspan="1" rowspan="1" style="vertical-align:top;">4-Year OS</th><th colspan="1" rowspan="1" style="vertical-align:top;">Treatment (refer to <a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__388/?report=objectonly" target="object" rid-figpopup="figCDR0000062789388" rid-ob="figobCDR0000062789388">Table 2</a> for chemotherapy regimen descriptions)</th></tr></thead><tbody><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FH (all patients)</td><td colspan="1" rowspan="1" style="vertical-align:top;">88% EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">97%</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling followed by abdominal XRT and regimen DD-4A</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FH (without LOH of 1p and/or 16q) and positive lymph nodes</td><td colspan="1" rowspan="1" style="vertical-align:top;">85%
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EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">97%</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling followed by abdominal XRT and regimen DD-4A</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FH (without LOH of 1p and/or 16q) and negative lymph nodes</td><td colspan="1" rowspan="1" style="vertical-align:top;">97% EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">99%</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling followed by abdominal XRT and regimen DD-4A</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FH (with LOH of 1p and 16q) (n = 31)</td><td colspan="1" rowspan="1" style="vertical-align:top;">87% EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">94%</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling followed by abdominal XRT and regimen M</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FA</td><td colspan="1" rowspan="1" style="vertical-align:top;">88% RFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">100% (n = 8)</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling followed by abdominal XRT and regimen DD-4A</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FA (preoperative treatment)</td><td colspan="1" rowspan="1" style="vertical-align:top;">71% RFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">71% (n = 7)</td><td colspan="1" rowspan="1" style="vertical-align:top;">Preoperative treatment with regimen DD-4A followed by nephrectomy + lymph node sampling and abdominal XRT</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">DA </td><td colspan="1" rowspan="1" style="vertical-align:top;">46% EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">53% (n = 16)</td><td colspan="1" rowspan="1" style="vertical-align:top;">Preoperative treatment with regimen I followed by nephrectomy + lymph node sampling and abdominal XRT</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">DA</td><td colspan="1" rowspan="1" style="vertical-align:top;">82% EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">91% (n = 23)</td><td colspan="1" rowspan="1" style="vertical-align:top;">Immediate nephrectomy + lymph node sampling followed by abdominal XRT and regimen UH1</td></tr></tbody></table></div><div><div><dl class="temp-labeled-list small"><dt></dt><dd><div><p class="no_margin">DA = diffuse anaplastic; EFS = event-free survival; FA = focal anaplastic; FH = favorable histology; LOH = loss of heterozygosity; OS = overall survival; RFS = relapse-free survival; XRT = radiation therapy.</p></div></dd><dt></dt><dd><div><p class="no_margin"><sup>a</sup>Source: Grundy et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_101">101</a>] Dome et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_152">152</a>] Fernandez et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_233">233</a>] Dix et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_220">220</a>] and Daw et al.[<a class="bk_pop" href="#CDR0000062789_rl_1_223">223</a>]</p></div></dd></dl></div></div></div><div id="CDR0000062789__2005"><h5>Radiation therapy</h5><p id="CDR0000062789__1924">Early initiation of radiation therapy is a critical component of multimodal therapy for patients with nonmetastatic Wilms tumor. In a review of 1,488 patients with Wilms tumor who underwent surgery and radiation therapy, a surgery-to-radiation therapy interval of greater than 14 days was associated with an increased risk of mortality (hazard ratio, 2.13; <i>P</i> = .013). This underscores the importance of initiating radiation therapy within 14 days of surgery, which is specified in Wilms tumor treatment protocols.[<a class="bk_pop" href="#CDR0000062789_rl_1_221">221</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335150/" class="def">Level of evidence: 3iiiA</a>]</p></div><div id="CDR0000062789__2006"><h5>Loss of heterozygosity of 1p or 16q</h5><p id="CDR0000062789__984">Loss of heterozygosity of 1p or 16q was shown to influence EFS but not OS in 588 patients with stage III FH Wilms tumor treated on the COG AREN0532 protocol. When combined, lymph node status and loss of heterozygosity status provided a strong predictor of excellent EFS and OS when both were absent, with a 4-year EFS rate of 97%, and an OS rate of 99%.[<a class="bk_pop" href="#CDR0000062789_rl_1_233">233</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335135/" class="def">Level of evidence: 2Di</a>] The outcome was poorer for patients having both positive lymph nodes and loss of heterozygosity of 1p or 16q, with a 4-year EFS rate of 74%. However, the 4-year OS rate was not influenced, at 92%.[<a class="bk_pop" href="#CDR0000062789_rl_1_233">233</a>] On the basis of these results, therapy was augmented for patients with loss of heterozygosity of 1p/16q for patients enrolled on the AREN0533 trial. Patients with stage III and stage IV Wilms tumor with loss of heterozygosity were treated with regimen M. The 4-year EFS rate was 90.2%, and the OS rate was 96.1%, compared with a 4-year EFS rate of 61.3% (<i>P</i> = .001) and a 4-year OS rate of 86.0% (<i>P</i> = .087) for patients in the NWTS-5 trial. There was a suggestion of improvement in survival; however, the study was not powered to detect differences in survival.[<a class="bk_pop" href="#CDR0000062789_rl_1_220">220</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335153/" class="def">Level of evidence: 3iiiDi</a>]</p></div><div id="CDR0000062789__TrialSearch_982_sid_5"><h5>Current Clinical Trials</h5><p id="CDR0000062789__TrialSearch_982_22">Use our <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/advanced-search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">advanced clinical trial search</a> to find NCI-supported cancer clinical trials that are now enrolling patients. The search can be narrowed by location of the trial, type of treatment, name of the drug, and other criteria. <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">General information</a> about clinical trials is also available.</p></div></div><div id="CDR0000062789__986"><h4>Treatment of stage IV Wilms tumor</h4><p id="CDR0000062789__987"><a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__933/?report=objectonly" target="object" rid-figpopup="figCDR0000062789933" rid-ob="figobCDR0000062789933"> Table 7</a> provides an overview of the standard treatment options and survival data for patients with <a href="#CDR0000062789__40">stage IV Wilms tumor</a>, based on published results. </p><div id="CDR0000062789__933" class="table"><h3><span class="title">Table 7. Overview of Standard Treatment Options for Stage IV Wilms Tumor<sup>a</sup></span></h3><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK65842.23/table/CDR0000062789__933/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__CDR0000062789__933_lrgtbl__"><table class="no_margin"><thead><tr><th colspan="1" rowspan="1" style="vertical-align:top;">Histology</th><th colspan="1" rowspan="1" style="vertical-align:top;">4-Year RFS or EFS</th><th colspan="1" rowspan="1" style="vertical-align:top;">4-Year OS</th><th colspan="1" rowspan="1" style="vertical-align:top;">Treatment (refer to <a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__388/?report=objectonly" target="object" rid-figpopup="figCDR0000062789388" rid-ob="figobCDR0000062789388">Table 2</a> for chemotherapy regimen descriptions)</th></tr></thead><tbody><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FH</td><td colspan="1" rowspan="1" style="vertical-align:top;">76% RFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">86%</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling, followed by abdominal XRT,<sup>b</sup> radiation to sites of metastases, bilateral pulmonary XRT,<sup>c</sup> and regimen DD-4A</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FH (with isolated lung nodules)</td><td colspan="1" rowspan="1" style="vertical-align:top;">85%
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EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">96%</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling, followed by abdominal XRT,<sup>b</sup> +/- bilateral pulmonary XRT,<sup>c</sup> and regimen DD-4A or regimen M<sup>d</sup></td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FH (with isolated lung nodules with CR to DD-4A)</td><td colspan="1" rowspan="1" style="vertical-align:top;">83% EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">94%</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling, followed by abdominal XRT<sup>b</sup> and regimen DD-4A</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FH (with isolated lung nodules with incomplete response to DD-4A)</td><td colspan="1" rowspan="1" style="vertical-align:top;">92% EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">96%</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling, followed by abdominal XRT<sup>b</sup> and bilateral pulmonary XRT<sup>c</sup> and regimen M</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FH (with LOH of 1p and/or 16q) (n = 20)</td><td colspan="1" rowspan="1" style="vertical-align:top;">95% EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">100%</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling, abdominal XRT<sup>b</sup> radiation to sites of metastases<sup>b</sup>, and regimen M</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">FA</td><td colspan="1" rowspan="1" style="vertical-align:top;">61%
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EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">72% (n = 11)</td><td colspan="1" rowspan="1" style="vertical-align:top;">Nephrectomy + lymph node sampling, followed by abdominal XRT,<sup>b</sup> radiation to sites of metastases, bilateral pulmonary XRT,<sup>c</sup> and regimen DD-4A</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">DA</td><td colspan="1" rowspan="1" style="vertical-align:top;">33% EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">33% (n = 10)</td><td colspan="1" rowspan="1" style="vertical-align:top;">Immediate nephrectomy + lymph node sampling followed by abdominal XRT,<sup>b</sup> radiation to sites of metastases, whole-lung XRT,<sup>c</sup> and regimen I</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">DA (preoperative treatment)</td><td colspan="1" rowspan="1" style="vertical-align:top;">60% EFS</td><td colspan="1" rowspan="1" style="vertical-align:top;">70% (n = 10)</td><td colspan="1" rowspan="1" style="vertical-align:top;">Preoperative treatment with regimen UH2 followed by nephrectomy + lymph node sampling, followed by abdominal XRT,<sup>b</sup> radiation to sites of metastases, and whole-lung XRT<sup>c</sup>
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</td></tr></tbody></table></div><div><div><dl class="temp-labeled-list small"><dt></dt><dd><div><p class="no_margin">CR = complete response; DA = diffuse anaplasia; EFS = event-free survival; FA = focal anaplasia; FH = favorable histology; LOH = loss of heterozygosity; OS = overall survival; RFS = relapse-free survival; XRT = radiation therapy.</p></div></dd><dt></dt><dd><div><p class="no_margin"><sup>a</sup>Source: Grundy et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_101">101</a>] Dome et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_152">152</a>] Dix et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_222">222</a>] Dix et al.,[<a class="bk_pop" href="#CDR0000062789_rl_1_220">220</a>] and Daw et al.[<a class="bk_pop" href="#CDR0000062789_rl_1_223">223</a>]</p></div></dd><dt></dt><dd><div><p class="no_margin"><sup>b</sup>Abdominal XRT is planned according to local stage of renal tumor. </p></div></dd><dt></dt><dd><div><p class="no_margin"><sup>c</sup>Pulmonary XRT is reserved for patients with chest x-ray/chest computed tomography evidence of pulmonary metastases.</p></div></dd><dt></dt><dd><div><p class="no_margin"><sup>d</sup>Refer to the <a href="https://www.cancer.gov/clinicaltrials/NCT00379340" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0533 (NCT00379340)</a> study for more information.</p></div></dd></dl></div></div></div><p id="CDR0000062789__988">Stage IV disease is defined by the presence of hematogenous metastases to the lung, liver, bone, brain, or other sites, with the lung being the most common site. The presence of liver metastases at diagnosis is not an independent adverse prognostic factor in patients with stage IV Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_200">200</a>]</p><div id="CDR0000062789__2007"><h5>Treatment of pulmonary nodules and metastases</h5><p id="CDR0000062789__2008">Historically, chest x-rays were used to detect pulmonary metastases. The introduction of CT created controversy because many patients had lung nodules detected by chest CT scans that were not seen on chest x-rays. Management of newly diagnosed patients with FH Wilms tumor who have lung nodules detected only by CT scans (with negative chest x-ray) has elicited controversy as to whether they need to be treated with additional intensive treatment that is accompanied by acute and late toxicities.</p><p id="CDR0000062789__989">Evidence (treatment of pulmonary nodules detected by chest CT scan only):</p><ol id="CDR0000062789__990"><li class="half_rhythm"><div>A retrospective review of 186 patients from NWTS-4 and <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5</a> with CT-only–detected lung nodules reported on the use of doxorubicin, vincristine, and dactinomycin versus the use of two drugs.[<a class="bk_pop" href="#CDR0000062789_rl_1_234">234</a>]<ul id="CDR0000062789__800"><li class="half_rhythm"><div>Patients who received doxorubicin, vincristine, and dactinomycin with or without lung irradiation had a 5-year EFS rate of 80% versus an EFS rate of 56% for patients receiving only two drugs (<i>P</i> = .004). </div></li><li class="half_rhythm"><div>There was no difference in EFS according to whether the lung was irradiated.</div></li><li class="half_rhythm"><div>There was no difference in the 5-year OS rate (87% vs. 86%).</div></li></ul></div></li></ol><p id="CDR0000062789__992">Retrospective studies from Europe have examined the impact of omitting pulmonary radiation in patients with pulmonary metastases diagnosed by chest x-ray. European investigators omitted radiation from the treatment of most patients with Wilms tumor and pulmonary metastases as identified on chest x-ray who were treated on the <a href="https://www.cancer.gov/clinicaltrials/NCT00003804" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">SIOP-93-01 (NCT00003804)</a> trial. The European approach to renal tumors differs from the approach used in North America. All patients who were shown to have a renal tumor by imaging underwent 9 weeks of prenephrectomy chemotherapy consisting of vincristine, dactinomycin, and doxorubicin. </p><p id="CDR0000062789__993">Evidence (omission of pulmonary irradiation):</p><ol id="CDR0000062789__994"><li class="half_rhythm"><div>In a retrospective SIOP study, 234 newly diagnosed patients with Wilms tumor presenting with pulmonary metastases were treated according to the response of the pulmonary metastases to the prenephrectomy chemotherapy.[<a class="bk_pop" href="#CDR0000062789_rl_1_235">235</a>] <ol id="CDR0000062789__1023" class="lower-alpha"><li class="half_rhythm"><div>Patients who were in complete remission (67%) after 6 weeks of therapy continued with the same chemotherapy and did not require radiation to their lungs. <ul id="CDR0000062789__1024"><li class="half_rhythm"><div>The 5-year EFS rate was 77%, and the OS rate was 88%.</div></li></ul></div></li><li class="half_rhythm"><div>Patients who had residual pulmonary metastases were evaluated for metastasectomy.<ul id="CDR0000062789__1025"><li class="half_rhythm"><div>Thirty-seven patients (17%) obtained complete remission with surgery, and their outcome was similar to that of the group of patients who were treated with chemotherapy. Tumor viability in the resected pulmonary metastases was not a factor for omitting radiation therapy.</div></li><li class="half_rhythm"><div> The 5-year EFS rate was 84%, and the OS rate was 92%.</div></li></ul></div></li><li class="half_rhythm"><div>Patients with residual pulmonary metastases that were incompletely resected or inoperable received more aggressive chemotherapy consisting of ifosfamide/anthracycline alternating with carboplatin/etoposide for 9 weeks. <ul id="CDR0000062789__1026"><li class="half_rhythm"><div>Patients showing a complete remission at that time were spared pulmonary radiation and continued with chemotherapy, whereas patients with residual pulmonary metastases continued with additional chemotherapy (to complete 34 weeks) and pulmonary irradiation. The 5-year OS rate was 48%, compared with the OS rates for patients who responded to chemotherapy alone (88%) and those who underwent metastasectomy (92%) (<i>P</i> < .001).</div></li><li class="half_rhythm"><div>Patients with high-risk histologies, such as anaplastic Wilms tumor, were treated with more aggressive chemotherapy but had a poorer outcome, compared with that of patients with nonanaplastic histologies (5-year OS rate, 33% vs. 87%; <i>P</i> < .001).</div></li></ul></div></li></ol></div></li><li class="half_rhythm"><div>Based on the European experience, the COG <a href="https://www.cancer.gov/clinicaltrials/NCT00379340" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0533 (NCT00379340)</a> study applied a new strategy for patients with FH Wilms tumor and isolated lung metastases to improve EFS while reducing exposure to lung irradiation. Therapy was adjusted on the basis of lung nodule response and tumor-specific loss of heterozygosity at 1p and 16q.[<a class="bk_pop" href="#CDR0000062789_rl_1_222">222</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335153/" class="def">Level of evidence: 3iiiDi</a>]<ul id="CDR0000062789__1868"><li class="half_rhythm"><div>Of the 292 patients enrolled in the study, 133 patients (42%) showed a complete lung nodule response after 6 weeks of DD-4A (vincristine, dactinomycin, doxorubicin) and continued receiving the same chemotherapy without lung radiation therapy. The 4-year EFS rate was 80%, and OS rate was 96%.</div></li><li class="half_rhythm"><div>Patients who had an incomplete lung nodule response (n = 145) or loss of heterozygosity at 1p/16q (n = 18) received lung radiation therapy and four cycles of cyclophosphamide/etoposide in addition to the DD-4A drugs (regimen M). The 4-year EFS rate was 89%, and the OS rate was 95% for the incomplete lung nodule response group without loss of heterozygosity. Of the patients with pulmonary metastases only and loss of heterozygosity, the 4-year EFS and OS rates were 100%.</div></li><li class="half_rhythm"><div>In a post hoc analysis of 1q gain in 212 patients enrolled in AREN0533 who had DNA available, patients with lung nodule complete remission with 1q gain had a significantly worse 4-year EFS rate (57% vs. 86%, <i>P</i> = .001) and trend toward inferior OS rates (89% vs. 97%). Relapses were predominantly pulmonary. There was no difference in outcome for patients with incomplete lung nodule response on the basis of 1q gain.</div></li><li class="half_rhythm"><div>Regimen M (refer to <a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__388/?report=objectonly" target="object" rid-figpopup="figCDR0000062789388" rid-ob="figobCDR0000062789388">Table 2</a>) has a higher potential for late effects (increased risk of secondary leukemias and risk of infertility related to a cumulative dose of cyclophosphamide of 8.8 g/m<sup>2</sup>).</div></li><li class="half_rhythm"><div>COG showed that initial lung radiation therapy could be avoided in approximately 40% of patients. OS was excellent; however, there was a trend toward more events than expected (expected, 15% and observed, 20%; <i>P</i> = .052).</div></li></ul></div></li></ol><p id="CDR0000062789__1869">Although fewer patients were spared pulmonary radiation when treated in the COG trial than in the European trials, it is important to note several differences between the studies and why the studies cannot be directly compared.[<a class="bk_pop" href="#CDR0000062789_rl_1_222">222</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_235">235</a>] Patients in Europe receive a more dose-dense regimen of dactinomycin and doxorubicin before their pulmonary metastases are reevaluated than do patients in North America (135 ug/kg dactinomycin and 100 mg/m<sup>2</sup> doxorubicin in Europe, compared with 45 ug/kg dactinomycin and 45 mg/m<sup>2</sup> of doxorubicin in North America). European studies allow lung radiation therapy to be omitted for patients with a complete remission achieved by chemotherapy or pulmonary metastasectomy, whereas radiation therapy was only omitted in the United States for patients with a complete remission with chemotherapy alone. Imaging studies were not centrally reviewed in the European studies, whereas they were in the United States, and the definition of complete remission may have been more stringent in the <a href="https://www.cancer.gov/clinicaltrials/NCT00379340" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0533 (NCT00379340)</a> trial.</p></div><div id="CDR0000062789__2009"><h5>Treatment of stage IV diffuse anaplastic Wilms tumor</h5><p id="CDR0000062789__1965">In the <a href="https://www.cancer.gov/clinicaltrials/NCT00335556" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0321 (NCT00335556)</a> study, the combination of vincristine and irinotecan (VI) was tested in an upfront window for patients with diffuse anaplastic Wilms tumor and measurable disease.[<a class="bk_pop" href="#CDR0000062789_rl_1_223">223</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335155/" class="def">Level of evidence: 3iiiDii</a>]</p><ul id="CDR0000062789__2018"><li class="half_rhythm"><div>Fourteen patients with stage IV diffuse anaplastic Wilms tumor with measurable disease received the window therapy; one patient achieved a complete response (CR), ten patients achieved partial responses (PRs), and no patients had stable disease. This resulted in a CR and PR rate of 79%.</div></li><li class="half_rhythm"><div>Patients who responded to VI in the window therapy had VI incorporated into their regimen (UH2).</div></li><li class="half_rhythm"><div>Because of the observed cardiac/pulmonary toxicities encountered in this trial, the study was interrupted and amended with reduced doses of doxorubicin, cyclophosphamide, and etoposide (when combined with carboplatin).</div></li><li class="half_rhythm"><div>Further study of the modified regimen is planned in patients with newly diagnosed diffuse anaplastic Wilms tumor.</div></li></ul></div><div id="CDR0000062789__TrialSearch_986_sid_6"><h5>Current Clinical Trials</h5><p id="CDR0000062789__TrialSearch_986_22">Use our <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/advanced-search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">advanced clinical trial search</a> to find NCI-supported cancer clinical trials that are now enrolling patients. The search can be narrowed by location of the trial, type of treatment, name of the drug, and other criteria. <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">General information</a> about clinical trials is also available.</p></div></div><div id="CDR0000062789__601"><h4>Treatment of stage V Wilms tumor and those predisposed to developing bilateral Wilms tumor</h4><p id="CDR0000062789__945">Currently, there is not a standard approach for the treatment of <a href="#CDR0000062789__42">stage V Wilms tumor</a> (bilateral Wilms tumor at diagnosis) and those predisposed to developing bilateral Wilms tumor; however, for the first time, a prospective study of the treatment of patients with bilateral Wilms tumor has been completed and provides guidance for the approach.[<a class="bk_pop" href="#CDR0000062789_rl_1_144">144</a>]</p><p id="CDR0000062789__637">Management of a child with bilateral Wilms tumor is very challenging. The goals of therapy are to eradicate all tumor and to preserve as much normal renal tissue as possible, with the hope of decreasing the risk of chronic renal failure among these children.[<a class="bk_pop" href="#CDR0000062789_rl_1_236">236</a>] </p><p id="CDR0000062789__807">Historically, based on the NWTS-4 and <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5</a> trials and trials performed in Europe, patients with bilateral Wilms tumor have had a lower EFS and OS than have patients with localized Wilms tumor. The NWTS-4 study reported that the 8-year EFS rate for patients with bilateral FH Wilms tumor was 74%, and the OS rate was 89%; for patients with anaplastic histology, the EFS rate was 40%, and the OS rate was 45%.[<a class="bk_pop" href="#CDR0000062789_rl_1_166">166</a>] The NWTS-5 study reported that the 4-year EFS rate for all bilateral Wilms tumor patients was 56%, and the OS rate was 81%; the 4-year EFS rates for patients with FH (65%), focal anaplastic histology (76%), and diffuse anaplastic histology (25%) were also reported.[<a class="bk_pop" href="#CDR0000062789_rl_1_101">101</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_152">152</a>] Similar outcomes for patients with bilateral Wilms tumor have been reported in Europe.[<a class="bk_pop" href="#CDR0000062789_rl_1_165">165</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_237">237</a>] In a single-institution experience in the Netherlands (N = 41), there was significant morbidity in terms of renal failure (32%) and secondary tumors (20%).[<a class="bk_pop" href="#CDR0000062789_rl_1_237">237</a>] The incidence of end-stage renal failure in the Dutch study may be a reflection of a longer follow-up period.</p><p id="CDR0000062789__1299">Treatment options for stage V (bilateral) Wilms tumor include the following:</p><ol id="CDR0000062789__1300"><li class="half_rhythm"><div><a href="#CDR0000062789__774">Preoperative chemotherapy and resection</a>.</div></li><li class="half_rhythm"><div><a href="#CDR0000062789__778">Renal transplant</a>.</div></li></ol><div id="CDR0000062789__774"><h5>Preoperative chemotherapy and resection</h5><p id="CDR0000062789__1872">For patients with bilateral Wilms tumor, the goal of therapy is to preserve as much renal tissue as possible without compromising overall outcome. This approach is used to avoid the late effect of end-stage renal disease, which can be caused by underlying germline genetic aberrations and treatment-related loss of functional renal tissue. End-stage renal disease occurs more frequently in patients with bilateral Wilms tumor (12% nonsyndromic) than in patients with unilateral Wilms tumor (<1%). Functional renal outcome is considerably better after bilateral nephron-sparing surgery than after other types of surgery.[<a class="bk_pop" href="#CDR0000062789_rl_1_144">144</a>]</p><p id="CDR0000062789__1278">Traditionally, patients have undergone bilateral renal biopsies, with staging of each kidney followed by preoperative chemotherapy. In the first prospective multi-institutional treatment trial (COG <a href="https://www.cancer.gov/clinicaltrials/NCT00945009" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0534 [NCT00945009]</a>), pretreatment biopsies were not required if results of imaging tests were consistent with Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_144">144</a>] This approach was taken because the bilateral occurrence of non-Wilms renal tumors is very low. Also, core-needle and wedge biopsies are not highly successful in identifying anaplasia in Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_143">143</a>] In the setting of an unusual clinical situation, such as age older than 10 years or atypical imaging features, when a diagnosis other than Wilms should be considered, a tissue diagnosis is obtained.[<a class="bk_pop" href="#CDR0000062789_rl_1_144">144</a>]</p><p id="CDR0000062789__1279">For patients who are treated with preoperative chemotherapy, the tumor pathology needs to be evaluated after 4 to 8 weeks. For patients not treated in a clinical trial, the ideal time to perform a biopsy or resection is unknown because minimal shrinkage may reflect chemotherapy-induced differentiation or anaplastic histology. A planned attempt at resection or biopsy of apparently unresectable tumor is undertaken no later than 12 weeks from diagnosis. Continuing therapy without evaluating tumor pathology in a patient with bilateral Wilms tumor may miss anaplastic histology or chemotherapy-induced differentiation (including rhabdomyomatous differentiation) and thus increase toxicity for the patient without providing additional benefit for tumor control. Anaplastic histology occurs in 10% of patients with bilateral Wilms tumor, and these tumors respond poorly to chemotherapy.[<a class="bk_pop" href="#CDR0000062789_rl_1_166">166</a>]</p><p id="CDR0000062789__1280">Once the diagnosis is confirmed, a complete resection is performed. Histologic confirmation of the diagnosis is not straightforward. In a series of 27 patients from NWTS-4, discordant pathology (unilateral anaplastic tumor) was seen in 20 cases (74%), which highlights the need to obtain tissue from both kidneys. Seven children who were later diagnosed with diffuse anaplastic tumors had core biopsies performed to establish the diagnosis; however, anaplasia was not found. Anaplasia was identified in only three of the nine patients when an open-wedge biopsy was performed and in seven of nine patients who had a partial or complete nephrectomy.[<a class="bk_pop" href="#CDR0000062789_rl_1_166">166</a>]</p><p id="CDR0000062789__1281">The decision to administer chemotherapy and/or radiation therapy after biopsy or a second-look
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operation is dependent on the tumor's response to initial therapy. More aggressive
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therapy is required for patients with inadequate response to initial therapy
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observed at the second procedure or in the setting of anaplasia.[<a class="bk_pop" href="#CDR0000062789_rl_1_176">176</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_238">238</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_239">239</a>]</p><p id="CDR0000062789__1840">End-stage renal disease is the most clinically significant morbidity in patients with bilateral Wilms tumor and can be caused by underlying germline genetic aberrations, as well as treatment-related loss of functional renal tissue. Long-term monitoring of renal function is required after treatment for bilateral disease.</p><p id="CDR0000062789__808">Evidence (preoperative chemotherapy and resection for bilateral Wilms tumor):</p><ol id="CDR0000062789__809"><li class="half_rhythm"><div>The first prospective study in bilateral Wilms tumor (<a href="https://www.cancer.gov/clinicaltrials/NCT00945009" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0534 [NCT00945009]</a>) aimed to improve EFS and OS while preserving renal tissue by intensifying preoperative chemotherapy (utilizing three drugs—vincristine, dactinomycin, and doxorubicin), completing definitive surgery by 12 weeks from diagnosis, and modifying postoperative chemotherapy on the basis of histologic response.[<a class="bk_pop" href="#CDR0000062789_rl_1_144">144</a>]<ul id="CDR0000062789__1841"><li class="half_rhythm"><div>For the arm that treated children with bilateral Wilms tumor, results showed that central review of imaging, surgical resection within 12 weeks of diagnosis, and response-based and histology-based postoperative therapy improved EFS and OS, when compared with the historical outcomes of children with bilateral Wilms tumor.</div></li><li class="half_rhythm"><div>For the 189 patients with bilateral Wilms tumor, 4-year EFS rate was 82.1% (95% confidence interval [CI], 73.5%–90.8%), and the OS rate was 94.9% (95% CI, 90.1%–99.7%). Because biopsy was not performed before treatment in this series, some of the patients enrolled may have had only nephrogenic rests and not a true Wilms tumor. This finding may have improved these survival figures over historical controls.</div></li><li class="half_rhythm"><div>One of the aims of the study was that 75% of patients undergo definitive surgery by 12 weeks. After induction chemotherapy, 163 of 189 patients (84%) underwent definitive surgical treatment in at least one kidney by 12 weeks, and 39% of patients retained parts of both kidneys.</div></li><li class="half_rhythm"><div>Chemotherapy after surgery was tailored according to histologic response. The 4-year EFS rate was 84.1% for FH tumors, 58.2% for anaplastic histology tumors, and 82% for blastemal-type tumors.</div></li><li class="half_rhythm"><div>Because of the higher risk of renal failure in patients with bilateral Wilms tumor than in patients with unilateral Wilms tumor, one of the goals of the study was that 50% of the patients undergo bilateral nephron-sparing surgery. This threshold was not met, with only 39% of patients successfully treated with bilateral nephron-sparing surgery.</div></li><li class="half_rhythm"><div>Based on the above study, the recommendation was to continue with three-drug preoperative chemotherapy for 6 to 12 weeks followed by nephron-sparing surgery whenever possible. After resection, postoperative therapy is based on the histology of the resected specimen. The disappointing use of nephron-sparing surgery in this study may have been because of the level of experience of the surgeons in this multi-institutional study.</div></li></ul></div></li><li class="half_rhythm"><div>In a retrospective review of 93 children with bilateral Wilms tumor registered at Associazione Italiana di Ematologia e Oncologia Pediatrica (AIEOP) centers over a 21-year period, 43 patients were treated with vincristine and dactinomycin preoperatively and 37 patients were treated with vincristine, dactinomycin, and doxorubicin. The duration of preoperative chemotherapy ranged from 1 week to 40 weeks (median, 12 weeks).[<a class="bk_pop" href="#CDR0000062789_rl_1_165">165</a>]<ul id="CDR0000062789__1867"><li class="half_rhythm"><div>The 4-year DFS rate was 67%, and the OS rate was 80%.</div></li><li class="half_rhythm"><div>There was a trend toward better EFS in nonmetastatic patients receiving vincristine, dactinomycin, and doxorubicin preoperatively (4-year EFS rate, 84%) than for patients receiving vincristine and dactinomycin (4-year EFS rate, 65%), but this was not significant.</div></li><li class="half_rhythm"><div>The bilateral renal parenchyma was preserved in 48% of patients.</div></li></ul></div></li><li class="half_rhythm"><div>In a retrospective review of 49 patients with Wilms tumor who received preoperative therapy according to the <a href="https://www.cancer.gov/clinicaltrials/NCT00003804" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">SIOP-93-01 (NCT00003804)</a> guidelines, the timing of surgery was determined when there was no longer imaging evidence of tumor regression. The mean treatment duration was 80 days before renal-sparing surgery.[<a class="bk_pop" href="#CDR0000062789_rl_1_240">240</a>] <ul id="CDR0000062789__810"><li class="half_rhythm"><div>The 5-year EFS rate was 83.4%, and the OS rate was 89.5%.</div></li><li class="half_rhythm"><div>All but one of the patients had renal-sparing surgery in at least one kidney.</div></li><li class="half_rhythm"><div>Despite the good survival, 14% of the patients developed end-stage renal disease.</div></li></ul></div></li><li class="half_rhythm"><div>In a retrospective review from St. Jude Children's Research Hospital, investigators described their experience with preoperative chemotherapy followed by renal-sparing procedures in children with bilateral FH Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_241">241</a>]<ul id="CDR0000062789__811"><li class="half_rhythm"><div>In a series, 39 of 42 patients with bilateral FH Wilms tumor underwent successful bilateral renal-sparing procedures after receiving preoperative chemotherapy. Three patients underwent unilateral nephrectomy with contralateral nephron-sparing surgery. Three patients required early (within 4 months) repeat nephron-sparing surgery for residual tumor. In the long term, seven patients had local tumor recurrence, and three patients had intestinal obstruction.</div></li><li class="half_rhythm"><div>The OS rate was 86% (mean follow-up, 4.1 years). Of the six patients who died, five had diffuse anaplastic histology.</div></li><li class="half_rhythm"><div>All of the patients had an estimated glomerular filtration rate of more than 60 mL/min/1.73m<sup>2</sup> at the last follow-up; none of the patients developed end-stage renal disease.</div></li><li class="half_rhythm"><div>The authors concluded that bilateral renal-sparing surgery is almost always feasible and can be done safely with good oncologic outcomes in patients with synchronous, bilateral Wilms tumor. It should be considered even if preoperative imaging studies suggest that the lesions are unresectable. Sparing of renal parenchyma is likely to help preserve renal function in children who are at significant risk of chronic renal insufficiency. Careful long-term follow-up is required to fully assess the potential progression of renal dysfunction.</div></li><li class="half_rhythm"><div>A follow-up review of these patients revealed the following: 8 of 36 patients underwent repeat nephron-sparing surgery, and an additional two patients required a third nephron-sparing surgery. Six of these patients were alive without disease at the 4.5-year follow-up. The two patients who died had blastemal-predominant histology.[<a class="bk_pop" href="#CDR0000062789_rl_1_242">242</a>]</div></li></ul></div></li></ol><p id="CDR0000062789__1907">(Refer to the <a href="#CDR0000062789__108">Treatment of Recurrent Childhood Kidney Tumors</a> section of this summary for information about recurrent disease.)</p></div><div id="CDR0000062789__1979"><h5>Treatment of patients with multicentric or bilaterally predisposed unilateral Wilms tumors</h5><p id="CDR0000062789__1980">On the basis of an identified subpopulation of patients with Wilms tumor who are at risk for metachronous disease, coupled with an increased risk of end-stage renal disease, the COG conducted the largest prospective study (<a href="https://www.cancer.gov/clinicaltrials/NCT00945009" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN0534 [NCT00945009]</a>) of these patients. The goal of this study was to preserve renal tissue while maintaining excellent overall outcomes.[<a class="bk_pop" href="#CDR0000062789_rl_1_3">3</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_84">84</a>]</p><p id="CDR0000062789__1981">Patients were identified by the treating institution as having a predisposition syndrome. Induction chemotherapy was determined by the presence of localized or metastatic disease found on imaging (and histology if a biopsy had been performed) at the time of diagnosis. Surgery, including renal-sparing surgery, was based on the radiographic response at 6 or 12 weeks, and additional chemotherapy was determined by histology. Patients with favorable histology and stage III or IV disease or any patient with anaplasia received radiation therapy.[<a class="bk_pop" href="#CDR0000062789_rl_1_243">243</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335150/" class="def">Level of evidence: 3iiiA</a>]</p><ul id="CDR0000062789__1982"><li class="half_rhythm"><div>Thirty-four patients were enrolled with the following underlying conditions: Beckwith-Wiedemann syndrome (n = 9), hemihypertrophy (n = 9), multicentric tumors (n = 10), WAGR syndrome (n = 2), solitary kidney (n = 2), Denys-Drash syndrome (n = 1), and Simpson-Golabi-Behmel syndrome (n = 1).</div></li><li class="half_rhythm"><div>The 4-year EFS and OS rates were 94% and 100%, respectively, with a median follow-up of 4.49 years. Two patients relapsed (one in the tumor bed and one in the abdomen); none of the deaths occurred during induction.</div></li><li class="half_rhythm"><div>Prenephrectomy chemotherapy facilitated renal preservation in 22 of 34 patients (65%). Eleven partial nephrectomies were performed after two cycles of chemotherapy, and nine partial nephrectomies were performed after four cycles of chemotherapy. Two of the tumors completely resolved after treatment with chemotherapy and required no subsequent surgery.</div></li><li class="half_rhythm"><div>There were 22 patients with a known predisposition syndrome for which routine ultrasonography screening would have been expected. Sixteen of these patients had stage I disease, three had stage II disease, and three had stage III disease. Thirteen of the tumors were detected through routine ultrasonography.</div></li><li class="half_rhythm"><div>These results suggest that a standardized treatment approach that includes preoperative chemotherapy, surgical resection within 6 to 12 weeks, and histology-based postoperative chemotherapy results in excellent EFS, OS, and preservation of renal parenchyma.</div></li></ul></div><div id="CDR0000062789__778"><h5>Renal transplant</h5><p id="CDR0000062789__779">Renal transplant for children with stage V Wilms tumor is usually delayed until 1 to 2 years have passed without evidence of malignancy because most relapses occur within 2 years of diagnosis.[<a class="bk_pop" href="#CDR0000062789_rl_1_244">244</a>] Similarly, renal transplant for children with Denys-Drash syndrome and Wilms tumor, all of whom require bilateral nephrectomy, is generally delayed 1 to 2 years after completion of initial treatment.[<a class="bk_pop" href="#CDR0000062789_rl_1_244">244</a>]</p></div><div id="CDR0000062789__403"><h5>Treatment options under clinical evaluation</h5><p id="CDR0000062789__1833">Information about National Cancer Institute (NCI)–supported clinical trials can be found on the <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NCI website</a>. For information about clinical trials sponsored by other organizations, refer to the <a href="https://clinicaltrials.gov/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">ClinicalTrials.gov website</a>.</p><div id="CDR0000062789__TrialSearch_403_sid_10"><h5>Current Clinical Trials</h5><p id="CDR0000062789__TrialSearch_403_22">Use our <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/advanced-search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">advanced clinical trial search</a> to find NCI-supported cancer clinical trials that are now enrolling patients. The search can be narrowed by location of the trial, type of treatment, name of the drug, and other criteria. <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">General information</a> about clinical trials is also available.</p></div></div></div><div id="CDR0000062789__1072"><h4>Follow-up after treatment</h4><p id="CDR0000062789__1073">For patients who have completed therapy for Wilms tumor and exhibit features consistent with genetic predisposition, such as bilateral Wilms tumor, screening involves renal ultrasonography examination every 3 months for metachronous tumors during the risk period for that particular syndrome (5 years for <i>WT1</i>-related syndromes; 8 years for Beckwith-Wiedemann syndrome).</p></div><div id="CDR0000062789__760"><h4>Late effects after Wilms tumor therapy</h4><p id="CDR0000062789__761">Children treated for Wilms tumor are
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at increased risk of developing the following:</p><ul id="CDR0000062789__1028"><li class="half_rhythm"><div><b>Premature mortality after Wilms tumor diagnosis. </b> In 1,441 5-year survivors of Wilms tumor, a substantial increase in cumulative mortality from 5.4% to 22.7% was noted from 30 to 50 years after Wilms tumor diagnosis. Excess deaths after 30 years were attributed to subsequent malignant neoplasms (50%) and cardiac-related causes (25%).[<a class="bk_pop" href="#CDR0000062789_rl_1_245">245</a>] Radiation therapy was a risk factor for both outcomes.</div></li><li class="half_rhythm"><div><b>Subsequent malignant neoplasms.</b>[<a class="bk_pop" href="#CDR0000062789_rl_1_245">245</a>-<a class="bk_pop" href="#CDR0000062789_rl_1_247">247</a>] Digestive cancers and breast cancer are the most frequent subsequent neoplasms, and radiation therapy is a risk factor. Women treated with lower doses of radiation to large volumes of breast tissue for a childhood cancer have a risk of breast cancer that is higher than previously recognized. The cumulative incidence of invasive breast cancer in Wilms tumor survivors who had received pulmonary radiation for metastatic Wilms tumor is nearly 15% by age 40 years.[<a class="bk_pop" href="#CDR0000062789_rl_1_248">248</a>]</div></li><li class="half_rhythm"><div><b>Congestive heart failure.</b> The risk of congestive heart failure is influenced by dose of doxorubicin received, radiation to the heart, and female sex.[<a class="bk_pop" href="#CDR0000062789_rl_1_247">247</a>,<a class="bk_pop" href="#CDR0000062789_rl_1_249">249</a>]</div></li><li class="half_rhythm"><div><b>Complications of pregnancy.</b>[<a class="bk_pop" href="#CDR0000062789_rl_1_250">250</a>] </div></li><li class="half_rhythm"><div><b>End-stage renal disease.</b> The cumulative incidence of end-stage renal disease caused by chronic renal failure at 20 years from diagnosis of Wilms tumor is low, at 3.1% for patients with bilateral Wilms tumor and less than 1% for those with unilateral Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_1_173">173</a>] Efforts, therefore, have been aimed
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toward reducing the intensity of therapy when possible.</div></li></ul><p id="CDR0000062789__67">Late renal effects in patients with Wilms and underlying genetic abnormalities include the following:</p><ul id="CDR0000062789__68"><li class="half_rhythm"><div>Children with WAGR syndrome or other germline <i>WT1</i> mutations are monitored throughout their lives because they are at increased risk of
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developing hypertension, nephropathy, and renal failure.[<a class="bk_pop" href="#CDR0000062789_rl_1_173">173</a>]</div></li><li class="half_rhythm"><div>Patients with
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Wilms tumor and aniridia without genitourinary abnormalities are at lower
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risk but are monitored for nephropathy or renal failure.[<a class="bk_pop" href="#CDR0000062789_rl_1_251">251</a>]</div></li><li class="half_rhythm"><div>Children with Wilms tumor and any genitourinary anomalies are also at increased risk of late renal failure and are monitored. Features associated with germline <i>WT1</i> mutations that increase the risk of developing renal failure include the following:[<a class="bk_pop" href="#CDR0000062789_rl_1_173">173</a>]<ul id="CDR0000062789__69"><li class="half_rhythm"><div> Stromal predominant histology.</div></li><li class="half_rhythm"><div>Bilateral disease.</div></li><li class="half_rhythm"><div>Intralobar nephrogenic rests.</div></li><li class="half_rhythm"><div>Wilms tumor diagnosed before age 2 years.</div></li></ul></div></li></ul><p id="CDR0000062789__1030">(Refer to the PDQ summary on <a href="/books/n/pdqcis/CDR0000343584/"> Late Effects of Treatment for Childhood Cancer</a> for a full discussion of the late effects of cancer treatment in children and adolescents.) </p></div></div><div id="CDR0000062789_rl_1"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_1_1">Howlader N, Noone AM, Krapcho M, et al.: SEER Cancer Statistics Review (CSR) 1975-2016. Bethesda, Md: National Cancer Institute, 2019. <a href="https://seer.cancer.gov/csr/1975_2016/" ref="pagearea=cite-ref&targetsite=external&targetcat=link&targettype=uri">Available online</a>. Last accessed October 29, 2020.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_2">Breslow N, Olshan A, Beckwith JB, et al.: Ethnic variation in the incidence, diagnosis, prognosis, and follow-up of children with Wilms' tumor. J Natl Cancer Inst 86 (1): 49-51, 1994. [<a href="https://pubmed.ncbi.nlm.nih.gov/8271283" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 8271283</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_3">Breslow N, Olshan A, Beckwith JB, et al.: Epidemiology of Wilms tumor. Med Pediatr Oncol 21 (3): 172-81, 1993.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_4">Horner MJ, Ries LA, Krapcho M, et al.: SEER Cancer Statistics Review, 1975-2006. Bethesda, Md: National Cancer Institute, 2009. <a href="https://seer.cancer.gov/archive/csr/1975_2006/" ref="pagearea=cite-ref&targetsite=external&targetcat=link&targettype=uri">Also available online</a>. Last accessed August 27, 2020.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_5">Scott RH, Stiller CA, Walker L, et al.: Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour. J Med Genet 43 (9): 705-15, 2006.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_6">Narod SA, Hawkins MM, Robertson CM, et al.: Congenital anomalies and childhood cancer in Great Britain. Am J Hum Genet 60 (3): 474-85, 1997.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_7">Vujanić GM, Apps JR, Moroz V, et al.: Nephrogenic rests in Wilms tumors treated with preoperative chemotherapy: The UK SIOP Wilms Tumor 2001 Trial experience. 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J Clin Oncol 18 (10): 2026-31, 2000. [<a href="https://pubmed.ncbi.nlm.nih.gov/10811666" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 10811666</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_22">Rump P, Zeegers MP, van Essen AJ: Tumor risk in Beckwith-Wiedemann syndrome: A review and meta-analysis. Am J Med Genet A 136 (1): 95-104, 2005. [<a href="https://pubmed.ncbi.nlm.nih.gov/15887271" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 15887271</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_23">Choufani S, Shuman C, Weksberg R: Molecular findings in Beckwith-Wiedemann syndrome. Am J Med Genet C Semin Med Genet 163C (2): 131-40, 2013. 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J Pediatr Surg 49 (1): 149-53, 2014.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_243">Ehrlich PF, Chi YY, Chintagumpala MM, et al.: Results of Treatment for Patients With Multicentric or Bilaterally Predisposed Unilateral Wilms Tumor (AREN0534): A report from the Children's Oncology Group. Cancer 126 (15): 3516-3525, 2020.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_244">Kist-van Holthe JE, Ho PL, Stablein D, et al.: Outcome of renal transplantation for Wilms' tumor and Denys-Drash syndrome: a report of the North American Pediatric Renal Transplant Cooperative Study. Pediatr Transplant 9 (3): 305-10, 2005.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_245">Wong KF, Reulen RC, Winter DL, et al.: Risk of Adverse Health and Social Outcomes Up to 50 Years After Wilms Tumor: The British Childhood Cancer Survivor Study. J Clin Oncol 34 (15): 1772-9, 2016.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_246">Breslow NE, Lange JM, Friedman DL, et al.: Secondary malignant neoplasms after Wilms tumor: an international collaborative study. Int J Cancer 127 (3): 657-66, 2010.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_247">Termuhlen AM, Tersak JM, Liu Q, et al.: Twenty-five year follow-up of childhood Wilms tumor: a report from the Childhood Cancer Survivor Study. Pediatr Blood Cancer 57 (7): 1210-6, 2011.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_248">Lange JM, Takashima JR, Peterson SM, et al.: Breast cancer in female survivors of Wilms tumor: a report from the national Wilms tumor late effects study. Cancer 120 (23): 3722-30, 2014.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_249">Green DM, Grigoriev YA, Nan B, et al.: Congestive heart failure after treatment for Wilms' tumor: a report from the National Wilms' Tumor Study group. J Clin Oncol 19 (7): 1926-34, 2001.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_250">Green DM, Lange JM, Peabody EM, et al.: Pregnancy outcome after treatment for Wilms tumor: a report from the national Wilms tumor long-term follow-up study. J Clin Oncol 28 (17): 2824-30, 2010.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1_251">Breslow NE, Takashima JR, Ritchey ML, et al.: Renal failure in the Denys-Drash and Wilms' tumor-aniridia syndromes. Cancer Res 60 (15): 4030-2, 2000.</div></li></ol></div></div><div id="CDR0000062789__432"><h2 id="_CDR0000062789__432_">Renal Cell Carcinoma (RCC)</h2><div id="CDR0000062789__742"><h3>Incidence of RCC</h3><p id="CDR0000062789__743">Malignant epithelial tumors arising in the kidneys of children account for more than 5% of new pediatric renal tumors; therefore, they are more common than clear cell sarcoma of the kidney or rhabdoid tumors of the kidney. The annual incidence rate is approximately 4 cases per 1 million children, compared with an incidence of Wilms tumor of the kidney that is at least 29-fold higher.[<a class="bk_pop" href="#CDR0000062789_rl_432_1">1</a>] </p><p id="CDR0000062789__1283">RCC, the most common primary malignancy of the kidney in adults, is rare in children younger than 15 years. In the older age group of adolescents (aged 15–19 years), approximately two-thirds of renal malignancies are RCC.[<a class="bk_pop" href="#CDR0000062789_rl_432_2">2</a>] Children and adolescents with RCC (n = 515) present with more advanced disease than do those aged 21 to 30 years.[<a class="bk_pop" href="#CDR0000062789_rl_432_1">1</a>]</p></div><div id="CDR0000062789__744"><h3>Conditions Associated With RCC</h3><p id="CDR0000062789__745">Conditions associated with RCC include the following: </p><ul id="CDR0000062789__600"><li class="half_rhythm"><div class="half_rhythm"><b>von Hippel-Lindau (VHL) disease.</b> VHL disease is an autosomal dominant condition in which blood vessels in the retina and cerebellum grow excessively.[<a class="bk_pop" href="#CDR0000062789_rl_432_3">3</a>] The gene for VHL disease is located on chromosome 3p26 and is a tumor-suppressor gene, which is either mutated or deleted in patients with the syndrome. </div><div class="half_rhythm">Screening for the <i>VHL</i> gene is available.[<a class="bk_pop" href="#CDR0000062789_rl_432_4">4</a>] Annual screening with abdominal ultrasonography or magnetic resonance imaging (MRI) is recommended, beginning at age 8 to 11 years, to detect clear cell renal carcinoma in these individuals when the lesions are smaller than 3 cm and renal-sparing surgery can be performed.[<a class="bk_pop" href="#CDR0000062789_rl_432_5">5</a>]</div><div class="half_rhythm">(Refer to the <a href="/books/n/pdqcis/CDR0000574548/#CDR0000574548__29">Von Hippel-Lindau Disease</a> section in the PDQ summary on <a href="/books/n/pdqcis/CDR0000574548/">Genetics of Kidney Cancer [Renal Cell Cancer]</a> for more information.)</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Tuberous sclerosis.</b> In tuberous sclerosis, the renal lesions may actually be epithelioid angiomyolipoma (also called perivascular epithelioid cell tumor or PEComa), which is associated with aggressive or malignant behavior and expresses melanocyte and smooth muscle markers.[<a class="bk_pop" href="#CDR0000062789_rl_432_6">6</a>,<a class="bk_pop" href="#CDR0000062789_rl_432_7">7</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Familial RCC.</b> Familial RCC has been associated with an inherited chromosome translocation involving chromosome 3.[<a class="bk_pop" href="#CDR0000062789_rl_432_8">8</a>] A high incidence of chromosome 3 abnormalities has also been demonstrated in nonfamilial renal tumors.</div><div class="half_rhythm"><i>SDHB</i>, <i>SDHC</i>, and <i>SDHD</i> are Krebs cycle enzyme genes that have been associated with the development of familial RCC occurring with pheochromocytoma/paraganglioma. Germline mutations in a subunit of the gene have been reported in individuals with renal cancer and no history of pheochromocytoma.[<a class="bk_pop" href="#CDR0000062789_rl_432_9">9</a>,<a class="bk_pop" href="#CDR0000062789_rl_432_10">10</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Renal medullary carcinoma.</b> A rare subtype of RCC, renal medullary carcinoma may be associated with sickle cell hemoglobinopathy.[<a class="bk_pop" href="#CDR0000062789_rl_432_11">11</a>]
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Renal medullary carcinomas are highly aggressive malignancies characterized clinically by a high stage at the time of detection, with widespread metastases and lack of response to chemotherapy
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and radiation therapy.[<a class="bk_pop" href="#CDR0000062789_rl_432_12">12</a>,<a class="bk_pop" href="#CDR0000062789_rl_432_13">13</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335144/" class="def"> Level of evidence: 3iiA</a>] Survival is poor and ranges from 2 weeks to 15 months, with a mean survival of 4 months.[<a class="bk_pop" href="#CDR0000062789_rl_432_11">11</a>,<a class="bk_pop" href="#CDR0000062789_rl_432_13">13</a>-<a class="bk_pop" href="#CDR0000062789_rl_432_16">16</a>] </div></li><li class="half_rhythm"><div class="half_rhythm"><b>Hereditary leiomyomatosis.</b> Hereditary leiomyomatosis (of skin and uterus) and RCC is a distinct phenotype caused by dominant inheritance of a mutation in the <i>FH</i> gene. Screening for RCC starting as early as age 5 years has been recommended.[<a class="bk_pop" href="#CDR0000062789_rl_432_17">17</a>,<a class="bk_pop" href="#CDR0000062789_rl_432_18">18</a>]</div></li><li class="half_rhythm"><div class="half_rhythm"><b>Previous treatment for childhood cancer.</b> Survivors of childhood cancer who were treated with radiation and/or chemotherapy are at a higher risk of developing renal cancers than are the general population. Highest risk has been observed among neuroblastoma survivors, with renal-directed radiation therapy of 5 Gy or more, and with platinum-based chemotherapy.[<a class="bk_pop" href="#CDR0000062789_rl_432_19">19</a>] Renal cancers have also been reported after treatment for rhabdomyosarcoma, leiomyosarcoma, acute lymphoblastic leukemia, primitive neuroectodermal tumors (PNET), and Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_432_20">20</a>-<a class="bk_pop" href="#CDR0000062789_rl_432_25">25</a>] (Refer to the <a href="/books/n/pdqcis/CDR0000343584/#CDR0000343584__116">Subsequent Neoplasms</a> section in the PDQ summary on <a href="/books/n/pdqcis/CDR0000343584/">Late Effects of Treatment for Childhood Cancer</a> for more information.)</div></li></ul></div><div id="CDR0000062789__746"><h3>Genetic Testing for Children and Adolescents With RCC</h3><p id="CDR0000062789__747">Indications for germline genetic testing of children and adolescents with RCC to check for a related syndrome are described in <a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__642/?report=objectonly" target="object" rid-figpopup="figCDR0000062789642" rid-ob="figobCDR0000062789642">Table 8</a>. (Refer to the PDQ summary on <a href="/books/n/pdqcis/CDR0000574548/">Genetics of Kidney Cancer [Renal Cell Cancer]</a> for more information.)</p><div id="CDR0000062789__642" class="table"><h3><span class="title">Table 8. Indications for Germline Genetic Analysis (Screening) of Children and Adolescents with Renal Cell Carcinoma (RCC)<sup>a</sup></span></h3><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK65842.23/table/CDR0000062789__642/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__CDR0000062789__642_lrgtbl__"><table class="no_margin"><thead><tr><th colspan="1" rowspan="1" style="vertical-align:top;"> Indication for Testing</th><th colspan="1" rowspan="1" style="vertical-align:top;">Tumor Histology</th><th colspan="1" rowspan="1" style="vertical-align:top;">Gene Test</th><th colspan="1" rowspan="1" style="vertical-align:top;">Related Syndrome</th></tr></thead><tbody><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Multifocal RCC or VHL lesions</td><td colspan="1" rowspan="1" style="vertical-align:top;">Clear cell</td><td colspan="1" rowspan="1" style="vertical-align:top;">
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<i>VHL</i> gene</td><td colspan="1" rowspan="1" style="vertical-align:top;">von Hippel-Lindau syndrome</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Family history of clear cell RCC or multifocal RCC with absent <i>VHL</i> mutation </td><td colspan="1" rowspan="1" style="vertical-align:top;">Clear cell </td><td colspan="1" rowspan="1" style="vertical-align:top;">Chromosome 3 gene translocations</td><td colspan="1" rowspan="1" style="vertical-align:top;"> Hereditary non-VHL clear cell RCC syndrome</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Multifocal papillary RCC or family history of papillary RCC</td><td colspan="1" rowspan="1" style="vertical-align:top;">Papillary</td><td colspan="1" rowspan="1" style="vertical-align:top;"><i>MET</i> gene</td><td colspan="1" rowspan="1" style="vertical-align:top;">Hereditary papillary RCC syndrome</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Multifocal RCC or cutaneous fibrofolliculoma or pulmonary cysts or spontaneous pneumothorax</td><td colspan="1" rowspan="1" style="vertical-align:top;">Chromophobe or oncocytic or clear cell</td><td colspan="1" rowspan="1" style="vertical-align:top;">Germline sequence <i>BHD</i> gene</td><td colspan="1" rowspan="1" style="vertical-align:top;">Birt-Hogg-Dubé syndrome</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Personal or family history of early-onset uterine leiomyomata or cutaneous leiomyomata </td><td colspan="1" rowspan="1" style="vertical-align:top;"><i>Type 2 papillary</i> or <i>collecting duct carcinoma</i></td><td colspan="1" rowspan="1" style="vertical-align:top;"><i>FH</i> gene</td><td colspan="1" rowspan="1" style="vertical-align:top;">Hereditary leiomyomata/RCC syndrome</td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Multifocal RCC or early-onset RCC or presence of paraganglioma/pheochromocytoma or family history of paraganglioma/pheochromocytoma</td><td colspan="1" rowspan="1" style="vertical-align:top;">Clear cell or chromophobe</td><td colspan="1" rowspan="1" style="vertical-align:top;"><i>SDHB</i> gene, <i>SDHC</i> gene, <i>SDHD</i> gene</td><td colspan="1" rowspan="1" style="vertical-align:top;">Hereditary paraganglioma/pheochromocytoma syndrome</td></tr></tbody></table></div><div><div><dl class="temp-labeled-list small"><dt></dt><dd><div><p class="no_margin">VHL = von Hippel-Lindau.</p></div></dd><dt></dt><dd><div><p class="no_margin"><sup>a</sup>Adapted from Linehan et al.[<a class="bk_pop" href="#CDR0000062789_rl_432_26">26</a>]</p></div></dd></dl></div></div></div></div><div id="CDR0000062789__1204"><h3>Genomics of RCC</h3><div id="CDR0000062789__sm_CDR0000777844_13"><h4>Molecular features of renal cell carcinoma</h4><p id="CDR0000062789__sm_CDR0000777844_15">Translocation-positive carcinomas of the kidney are recognized as a distinct form of renal cell carcinoma (RCC) and may be the most common form of RCC in children, accounting for 40% to 50% of pediatric RCC.[<a class="bk_pop" href="#CDR0000062789_rl_432_27">27</a>] In a Children's Oncology Group (COG) prospective clinical trial of 120 childhood and adolescent patients with RCC, nearly one-half of patients had translocation-positive RCC.[<a class="bk_pop" href="#CDR0000062789_rl_432_28">28</a>,<a class="bk_pop" href="#CDR0000062789_rl_432_29">29</a>] These carcinomas are characterized by translocations involving the<i> TFE3</i> gene located on Xp11.2. The <i>TFE3</i> gene may partner with one of the following genes:</p><ul id="CDR0000062789__sm_CDR0000777844_16"><li class="half_rhythm"><div><i>ASPSCR</i> in t(X;17)(p11.2;q25).</div></li><li class="half_rhythm"><div><i>PRCC</i> in t(X;1)(p11.2;q21).</div></li><li class="half_rhythm"><div><i>SFPQ</i> in t(X;1)(p11.2;p34).</div></li><li class="half_rhythm"><div><i>NONO</i> in inv(X;p11.2;q12).</div></li><li class="half_rhythm"><div><i>CLTC</i> in t(X;17)(p11;q23).</div></li></ul><p id="CDR0000062789__sm_CDR0000777844_17">Another less-common translocation subtype, t(6;11)(p21;q12), involving a <i>TFEB</i> gene fusion, induces overexpression of TFEB. The translocations involving <i>TFE3</i> and <i>TFEB</i> induce overexpression of these proteins, which can be identified by immunohistochemistry.[<a class="bk_pop" href="#CDR0000062789_rl_432_30">30</a>]</p><p id="CDR0000062789__sm_CDR0000777844_18">Previous exposure to chemotherapy is the only known risk factor for the development of Xp11 translocation RCCs. In one study, the postchemotherapy interval ranged from 4 to 13 years. All reported patients received either a DNA topoisomerase II inhibitor and/or an alkylating agent.[<a class="bk_pop" href="#CDR0000062789_rl_432_31">31</a>,<a class="bk_pop" href="#CDR0000062789_rl_432_32">32</a>]</p><p id="CDR0000062789__sm_CDR0000777844_19">Controversy exists as to the biological behavior of translocation RCC in children and young adults. Whereas some series have suggested a good prognosis when RCC is treated with surgery alone despite presenting at a more advanced stage (III/IV) than translocation-associated RCC, a meta-analysis reported that these patients have poorer outcomes.[<a class="bk_pop" href="#CDR0000062789_rl_432_33">33</a>-<a class="bk_pop" href="#CDR0000062789_rl_432_35">35</a>] The outcomes for these patients are being studied in the ongoing COG <a href="https://www.cancer.gov/clinicaltrials/NCT00898365" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN03B2 (NCT00898365)</a> biology and classification study. Vascular endothelial growth factor receptor–targeted therapies and mammalian target of rapamycin (mTOR) inhibitors seem to be active in Xp11 translocation metastatic RCC.[<a class="bk_pop" href="#CDR0000062789_rl_432_36">36</a>] Recurrences have been reported 20 to 30 years after initial resection of the translocation-associated RCC.[<a class="bk_pop" href="#CDR0000062789_rl_432_22">22</a>] </p><p id="CDR0000062789__sm_CDR0000777844_22">Diagnosis of Xp11 translocation RCC needs to be confirmed by a molecular genetic approach, rather than using <i>TFE3</i> immunohistochemistry alone, because reported cases have lacked the translocation.</p><p id="CDR0000062789__sm_CDR0000777844_25"> There is a rare subset of RCC cases that is positive for <i>TFE3</i> and lack a <i>TFE3</i> translocation, showing an <i>ALK</i> translocation instead. This subset of cases represents a newly recognized subgroup within RCC that is estimated to involve 15% to 20% of unclassified pediatric RCC. In the eight reported cases in children aged 6 to 16 years, the following was observed:[<a class="bk_pop" href="#CDR0000062789_rl_432_37">37</a>-<a class="bk_pop" href="#CDR0000062789_rl_432_40">40</a>]</p><ul id="CDR0000062789__sm_CDR0000777844_23"><li class="half_rhythm"><div><i>ALK</i> was fused to <i>VCL</i> in a t(2;10)(p23;q22) translocation (n = 3). The <i>VCL</i> translocation cases all occurred in children with the sickle cell trait, whereas none of the <i>TPM3</i> translocation cases did.</div></li><li class="half_rhythm"><div><i>ALK</i> was fused to <i>TPM3</i> (n = 3).</div></li><li class="half_rhythm"><div><i>ALK</i> was fused to <i>HOOK1</i> on 1p32 (n = 1).</div></li><li class="half_rhythm"><div>t(1;2) translocation fusing <i>ALK</i> and <i>TPM3</i> (n = 1).</div></li></ul></div></div><div id="CDR0000062789__748"><h3>Histology of RCC</h3><p id="CDR0000062789__749">Pediatric RCC differs histologically from the adult counterpart. Although the two main morphological subgroups of papillary and clear cell can be identified, about 25% of RCCs show heterogeneous features that do not fit into either of these categories.[<a class="bk_pop" href="#CDR0000062789_rl_432_3">3</a>] Childhood RCCs are more frequently of the papillary subtype (20%–50% of pediatric RCCs) and can sometimes occur in the setting of Wilms tumor, metanephric adenoma, and metanephric adenofibroma.[<a class="bk_pop" href="#CDR0000062789_rl_432_41">41</a>] </p><p id="CDR0000062789__1078">RCC in children and young adults has a different genetic and morphologic spectrum than that seen in older adults.[<a class="bk_pop" href="#CDR0000062789_rl_432_3">3</a>,<a class="bk_pop" href="#CDR0000062789_rl_432_32">32</a>,<a class="bk_pop" href="#CDR0000062789_rl_432_41">41</a>,<a class="bk_pop" href="#CDR0000062789_rl_432_42">42</a>]</p></div><div id="CDR0000062789__753"><h3>Prognosis and Prognostic Factors for RCC</h3><p id="CDR0000062789__1284">Prognostic factors for RCC include the following:</p><ul id="CDR0000062789__1285"><li class="half_rhythm"><div>Stage of disease.</div></li><li class="half_rhythm"><div>Lymph node involvement.</div></li></ul><p id="CDR0000062789__754">The primary prognostic factor for RCC is stage of disease. In 304 children and adolescents with RCC identified in the National Cancer Database, the median age was 13 years; 39% of patients presented with localized stage I disease, 16% with stage II disease, 33% with stage III disease, and 12% with stage IV disease. The 5-year overall survival (OS) rates were 100% for patients with stage I and stage II disease, 71% for stage III disease, and 8% for stage IV disease.[<a class="bk_pop" href="#CDR0000062789_rl_432_43">43</a>] Age and sex had no significant impact on survival. Survival was negatively impacted by increasing tumor size (<i>P</i> < .001), positive nodal status (<i>P</i> = .001), and higher pathologic stage (<i>P</i> < .001).[<a class="bk_pop" href="#CDR0000062789_rl_432_43">43</a>] The data attained in this article from the National Cancer Database are limited, as some patient details are not available and follow up is incomplete. Tumor size of 4 cm or smaller may or may not impact survival and local lymph node involvement may not be as significant in children. </p><p id="CDR0000062789__834">An important difference between the outcomes in children and adults with RCC is the prognostic significance of local lymph node involvement. Adults presenting with RCC and involved lymph nodes have a 5-year OS rate of approximately 20%, but the literature suggests that 72% of children with RCC and local lymph node involvement at diagnosis (without distant metastases) survive their disease.[<a class="bk_pop" href="#CDR0000062789_rl_432_27">27</a>] In another series of 49 patients from a population-based cancer registry, the findings were similar. In this series, 33% of the patients had papillary subtype, 22% had translocation type, 6% had clear-cell subtype, and 16% were unclassified. The survival rates at 5 years were 96% for patients with localized disease, 75% for patients with positive regional lymph nodes, and 33% for patients with distant metastatic RCC.[<a class="bk_pop" href="#CDR0000062789_rl_432_44">44</a>]</p><p id="CDR0000062789__2010"> In a COG prospective clinical trial of 40 patients with small (7 cm) primary tumors whose lymph nodes were adequately sampled, 19 had positive nodes.[<a class="bk_pop" href="#CDR0000062789_rl_432_28">28</a>] Outcome results of this trial are pending. </p></div><div id="CDR0000062789__961"><h3>Clinical Features and Diagnostic Evaluation of RCC</h3><p id="CDR0000062789__1032">RCC may present with the following:</p><ul id="CDR0000062789__1079"><li class="half_rhythm"><div>Abdominal mass.</div></li><li class="half_rhythm"><div>Abdominal pain.</div></li><li class="half_rhythm"><div>Hematuria.</div></li></ul><p id="CDR0000062789__962">Refer to the <a href="#CDR0000062789__898">Clinical Features of Wilms Tumor</a> and <a href="#CDR0000062789__900">Diagnostic and Staging Evaluation for Wilms Tumor</a> sections of this summary for more information about the clinical features and diagnostic evaluation of childhood kidney tumors. (Refer to the <a href="/books/n/pdqcis/CDR0000062894/#CDR0000062894__7">Stage Information for Renal Cell Cancer</a> section in the PDQ summary on adult <a href="/books/n/pdqcis/CDR0000062894/">Renal Cell Cancer Treatment</a> summary for more information about the staging evaluation.) </p></div><div id="CDR0000062789__257"><h3>Treatment of RCC</h3><p id="CDR0000062789__835">Survival of patients with RCC is affected by stage of disease at presentation and the completeness of resection at radical nephrectomy. OS rates for all patients with RCC range from 64% to 87%. The 5-year survival rates for pediatric RCC are 90% or higher for stage I, higher than 80% for stage II, 70% for stage III, and lower than 15% for stage IV.[<a class="bk_pop" href="#CDR0000062789_rl_432_27">27</a>] Retrospective analyses and the small number of patients involved place limitations on the level of evidence for specific treatment options for childhood RCC. </p><p id="CDR0000062789__836">Standard treatment options for RCC include the following:</p><ol id="CDR0000062789__837"><li class="half_rhythm"><div><a href="#CDR0000062789__1054">Radical nephrectomy with lymph node dissection</a>.</div></li><li class="half_rhythm"><div><a href="#CDR0000062789__1056">Renal-sparing surgery with lymph node dissection</a>.</div></li></ol><div id="CDR0000062789__1054"><h4>Radical nephrectomy with lymph node dissection</h4><p id="CDR0000062789__1055">The primary treatment for RCC includes total surgical removal of the kidney and associated lymph nodes.[<a class="bk_pop" href="#CDR0000062789_rl_432_27">27</a>]</p></div><div id="CDR0000062789__1056"><h4>Renal-sparing surgery with lymph node dissection</h4><p id="CDR0000062789__1057">Renal-sparing surgery may be considered for carefully selected patients with low-volume localized disease. In two small series, patients who had partial nephrectomies seemed to have outcomes equivalent to those who had radical nephrectomies.[<a class="bk_pop" href="#CDR0000062789_rl_432_32">32</a>,<a class="bk_pop" href="#CDR0000062789_rl_432_45">45</a>]</p></div><div id="CDR0000062789__1058"><h4>Other approaches</h4><p id="CDR0000062789__1059">As with adult RCC, there is no standard treatment for unresectable metastatic disease in children. The response to radiation therapy is poor, and chemotherapy is not effective. Immunotherapy with agents such as interferon-alpha and interleukin-2 may have some effect on cancer control.[<a class="bk_pop" href="#CDR0000062789_rl_432_46">46</a>,<a class="bk_pop" href="#CDR0000062789_rl_432_47">47</a>] Spontaneous regression of pulmonary metastasis rarely occurs with resection of the primary tumor. </p><p id="CDR0000062789__1060">Several targeted therapies (e.g., sorafenib, sunitinib, bevacizumab, temsirolimus, pazopanib, axitinib, and everolimus) have been approved for use in adults with RCC; however, these agents have not been tested in pediatric patients with RCC. Case reports of pediatric and adolescent patients with <i>TFE3</i> translocation–positive RCC suggest responsiveness to multiple tyrosine kinase inhibitors.[<a class="bk_pop" href="#CDR0000062789_rl_432_29">29</a>,<a class="bk_pop" href="#CDR0000062789_rl_432_48">48</a>,<a class="bk_pop" href="#CDR0000062789_rl_432_49">49</a>] Disease regression and improvement in symptoms have been reported with the use of cabozantinib in pediatric patients with translocation-positive RCC expressing MET.[<a class="bk_pop" href="#CDR0000062789_rl_432_50">50</a>] Any RCC that is positive for <i>TFE3</i> and lacks a translocation should be tested for ALK expression and translocation. Recognition of this subtype may lead to consideration of ALK inhibitor therapy.[<a class="bk_pop" href="#CDR0000062789_rl_432_37">37</a>]</p><p id="CDR0000062789__1235">(Refer to the PDQ summary on adult <a href="/books/n/pdqcis/CDR0000062894/">Renal Cell Cancer Treatment</a> for more information about the use of targeted therapies.)</p></div></div><div id="CDR0000062789__1895"><h3>Treatment Options Under Clinical Evaluation for RCC</h3><p id="CDR0000062789__1896">Information about National Cancer Institute (NCI)–supported clinical trials can be found on the <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NCI website</a>. For information about clinical trials sponsored by other organizations, refer to the <a href="https://clinicaltrials.gov/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">ClinicalTrials.gov website</a>.</p><p id="CDR0000062789__1897">The following is an example of a national and/or institutional clinical trial that is currently being conducted:</p><ul id="CDR0000062789__1898"><li class="half_rhythm"><div><b><a href="https://www.cancer.gov/clinicaltrials/NCT03595124" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">AREN1721 (NCT03595124)</a></b> (Axitinib and Nivolumab in Treating Participants With Unresectable or Metastatic <i>TFE</i>/Translocation RCC [tRCC])<b>:</b>
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<i>TFE</i>/tRCC is a distinct, typically translocation-associated RCC with characteristic morphology and immunohistochemical expression of <i>TFE3</i> or <i>TFEB</i>. Nearly 50% of pediatric RCCs are tRCC, and it accounts for 1% to 5% of RCCs overall, typically in the adolescent and young adult population. This is the first prospective therapeutic study of patients with tRCC. Patients aged 12 months and older who have histologically confirmed unresectable <i>TFE</i>/tRCC or metastatic <i>TFE</i>/tRCC diagnosed using WHO-defined criteria are eligible. Patients may be newly diagnosed or have received previous cancer therapy and must have measurable disease. Patients will be randomly assigned at the time of enrollment to one of two therapeutic arms: nivolumab or a combination of axitinib and nivolumab.</div></li></ul></div><div id="CDR0000062789__TrialSearch_432_sid_3"><h3>Current Clinical Trials</h3><p id="CDR0000062789__TrialSearch_432_22">Use our <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/advanced-search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">advanced clinical trial search</a> to find NCI-supported cancer clinical trials that are now enrolling patients. The search can be narrowed by location of the trial, type of treatment, name of the drug, and other criteria. <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">General information</a> about clinical trials is also available.</p></div><div id="CDR0000062789_rl_432"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_432_1">Akhavan A, Richards M, Shnorhavorian M, et al.: Renal cell carcinoma in children, adolescents and young adults: a National Cancer Database study. J Urol 193 (4): 1336-41, 2015.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_2">Bernstein L, Linet M, Smith MA, et al.: Renal tumors. In: Ries LA, Smith MA, Gurney JG, et al., eds.: Cancer incidence and survival among children and adolescents: United States SEER Program 1975-1995. Bethesda, Md: National Cancer Institute, SEER Program, 1999. NIH Pub.No. 99-4649, pp 79-90. <a href="http://seer.cancer.gov/publications/childhood/renal.pdf" ref="pagearea=cite-ref&targetsite=external&targetcat=link&targettype=uri">Also available online.</a> Last accessed June 08, 2020.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_3">Bruder E, Passera O, Harms D, et al.: Morphologic and molecular characterization of renal cell carcinoma in children and young adults. Am J Surg Pathol 28 (9): 1117-32, 2004.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_4">Schimke RN, Collins DL, Stolle CA: Von Hippel-Lindau syndrome. In: Pagon RA, Adam MP, Bird TD, et al., eds.: GeneReviews. Seattle, Wash: University of Washington, 1993-2018, pp. <a href="https://www.ncbi.nlm.nih.gov/books/NBK1463/" ref="pagearea=cite-ref&targetsite=external&targetcat=link&targettype=uri">Available online</a>. Last accessed June 08, 2020.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_5">Teplick A, Kowalski M, Biegel JA, et al.: Educational paper: screening in cancer predisposition syndromes: guidelines for the general pediatrician. Eur J Pediatr 170 (3): 285-94, 2011.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_6">Park HK, Zhang S, Wong MK, et al.: Clinical presentation of epithelioid angiomyolipoma. Int J Urol 14 (1): 21-5, 2007.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_7">Pea M, Bonetti F, Martignoni G, et al.: Apparent renal cell carcinomas in tuberous sclerosis are heterogeneous: the identification of malignant epithelioid angiomyolipoma. Am J Surg Pathol 22 (2): 180-7, 1998.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_8">Wang N, Perkins KL: Involvement of band 3p14 in t(3;8) hereditary renal carcinoma. Cancer Genet Cytogenet 11 (4): 479-81, 1984.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_9">Ricketts C, Woodward ER, Killick P, et al.: Germline SDHB mutations and familial renal cell carcinoma. J Natl Cancer Inst 100 (17): 1260-2, 2008.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_10">Linehan WM, Bratslavsky G, Pinto PA, et al.: Molecular diagnosis and therapy of kidney cancer. Annu Rev Med 61: 329-43, 2010.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_11">Swartz MA, Karth J, Schneider DT, et al.: Renal medullary carcinoma: clinical, pathologic, immunohistochemical, and genetic analysis with pathogenetic implications. Urology 60 (6): 1083-9, 2002.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_12">Sandberg JK, Mullen EA, Cajaiba MM, et al.: Imaging of renal medullary carcinoma in children and young adults: a report from the Children's Oncology Group. Pediatr Radiol 47 (12): 1615-1621, 2017.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_13">Hakimi AA, Koi PT, Milhoua PM, et al.: Renal medullary carcinoma: the Bronx experience. Urology 70 (5): 878-82, 2007.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_14">Strouse JJ, Spevak M, Mack AK, et al.: Significant responses to platinum-based chemotherapy in renal medullary carcinoma. Pediatr Blood Cancer 44 (4): 407-11, 2005.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_15">Rathmell WK, Monk JP: High-dose-intensity MVAC for Advanced Renal Medullary Carcinoma: Report of Three Cases and Literature Review. Urology 72 (3): 659-63, 2008.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_16">Ezekian B, Englum B, Gilmore BF, et al.: Renal medullary carcinoma: A national analysis of 159 patients. Pediatr Blood Cancer 64 (11): , 2017.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_17">Alrashdi I, Levine S, Paterson J, et al.: Hereditary leiomyomatosis and renal cell carcinoma: very early diagnosis of renal cancer in a paediatric patient. Fam Cancer 9 (2): 239-43, 2010.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_18">Bayley JP, Launonen V, Tomlinson IP: The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency. BMC Med Genet 9: 20, 2008.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_19">Wilson CL, Ness KK, Neglia JP, et al.: Renal carcinoma after childhood cancer: a report from the childhood cancer survivor study. J Natl Cancer Inst 105 (7): 504-8, 2013.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_20">Dhall D, Al-Ahmadie HA, Dhall G, et al.: Pediatric renal cell carcinoma with oncocytoid features occurring in a child after chemotherapy for cardiac leiomyosarcoma. Urology 70 (1): 178.e13-5, 2007.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_21">Schafernak KT, Yang XJ, Hsueh W, et al.: Pediatric renal cell carcinoma as second malignancy: reports of two cases and a review of the literature. Can J Urol 14 (6): 3739-44, 2007.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_22">Rais-Bahrami S, Drabick JJ, De Marzo AM, et al.: Xp11 translocation renal cell carcinoma: delayed but massive and lethal metastases of a chemotherapy-associated secondary malignancy. Urology 70 (1): 178.e3-6, 2007.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_23">Brassesco MS, Valera ET, Bonilha TA, et al.: Secondary PSF/TFE3-associated renal cell carcinoma in a child treated for genitourinary rhabdomyosarcoma. Cancer Genet 204 (2): 108-10, 2011.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_24">Breslow NE, Lange JM, Friedman DL, et al.: Secondary malignant neoplasms after Wilms tumor: an international collaborative study. Int J Cancer 127 (3): 657-66, 2010.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_25">Falzarano SM, McKenney JK, Montironi R, et al.: Renal Cell Carcinoma Occurring in Patients With Prior Neuroblastoma: A Heterogenous Group of Neoplasms. Am J Surg Pathol 40 (7): 989-97, 2016.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_26">Linehan WM, Pinto PA, Bratslavsky G, et al.: Hereditary kidney cancer: unique opportunity for disease-based therapy. Cancer 115 (10 Suppl): 2252-61, 2009.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_27">Geller JI, Dome JS: Local lymph node involvement does not predict poor outcome in pediatric renal cell carcinoma. Cancer 101 (7): 1575-83, 2004.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_28">Geller JI, Ehrlich PF, Cost NG, et al.: Characterization of adolescent and pediatric renal cell carcinoma: A report from the Children's Oncology Group study AREN03B2. Cancer 121 (14): 2457-64, 2015.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_29">Ambalavanan M, Geller JI: Treatment of advanced pediatric renal cell carcinoma. Pediatr Blood Cancer 66 (8): e27766, 2019.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_30">Argani P, Hicks J, De Marzo AM, et al.: Xp11 translocation renal cell carcinoma (RCC): extended immunohistochemical profile emphasizing novel RCC markers. Am J Surg Pathol 34 (9): 1295-303, 2010.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_31">Argani P, Laé M, Ballard ET, et al.: Translocation carcinomas of the kidney after chemotherapy in childhood. J Clin Oncol 24 (10): 1529-34, 2006.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_32">Ramphal R, Pappo A, Zielenska M, et al.: Pediatric renal cell carcinoma: clinical, pathologic, and molecular abnormalities associated with the members of the mit transcription factor family. Am J Clin Pathol 126 (3): 349-64, 2006.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_33">Geller JI, Argani P, Adeniran A, et al.: Translocation renal cell carcinoma: lack of negative impact due to lymph node spread. Cancer 112 (7): 1607-16, 2008.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_34">Camparo P, Vasiliu V, Molinie V, et al.: Renal translocation carcinomas: clinicopathologic, immunohistochemical, and gene expression profiling analysis of 31 cases with a review of the literature. Am J Surg Pathol 32 (5): 656-70, 2008.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_35">Qiu Rao, Bing Guan, Zhou XJ: Xp11.2 Translocation renal cell carcinomas have a poorer prognosis than non-Xp11.2 translocation carcinomas in children and young adults: a meta-analysis. Int J Surg Pathol 18 (6): 458-64, 2010.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_36">Malouf GG, Camparo P, Oudard S, et al.: Targeted agents in metastatic Xp11 translocation/TFE3 gene fusion renal cell carcinoma (RCC): a report from the Juvenile RCC Network. Ann Oncol 21 (9): 1834-8, 2010.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_37">Thorner PS, Shago M, Marrano P, et al.: TFE3-positive renal cell carcinomas are not always Xp11 translocation carcinomas: Report of a case with a TPM3-ALK translocation. Pathol Res Pract 212 (10): 937-942, 2016.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_38">Cajaiba MM, Jennings LJ, Rohan SM, et al.: ALK-rearranged renal cell carcinomas in children. Genes Chromosomes Cancer 55 (5): 442-51, 2016.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_39">Smith NE, Deyrup AT, Mariño-Enriquez A, et al.: VCL-ALK renal cell carcinoma in children with sickle-cell trait: the eighth sickle-cell nephropathy? Am J Surg Pathol 38 (6): 858-63, 2014.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_40">Cajaiba MM, Jennings LJ, George D, et al.: Expanding the spectrum of ALK-rearranged renal cell carcinomas in children: Identification of a novel HOOK1-ALK fusion transcript. Genes Chromosomes Cancer 55 (10): 814-7, 2016.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_41">Estrada CR, Suthar AM, Eaton SH, et al.: Renal cell carcinoma: Children's Hospital Boston experience. Urology 66 (6): 1296-300, 2005.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_42">Carcao MD, Taylor GP, Greenberg ML, et al.: Renal-cell carcinoma in children: a different disorder from its adult counterpart? Med Pediatr Oncol 31 (3): 153-8, 1998.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_43">Rialon KL, Gulack BC, Englum BR, et al.: Factors impacting survival in children with renal cell carcinoma. J Pediatr Surg 50 (6): 1014-8, 2015.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_44">Selle B, Furtwängler R, Graf N, et al.: Population-based study of renal cell carcinoma in children in Germany, 1980-2005: more frequently localized tumors and underlying disorders compared with adult counterparts. Cancer 107 (12): 2906-14, 2006.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_45">Cook A, Lorenzo AJ, Salle JL, et al.: Pediatric renal cell carcinoma: single institution 25-year case series and initial experience with partial nephrectomy. J Urol 175 (4): 1456-60; discussion 1460, 2006.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_46">Fyfe G, Fisher RI, Rosenberg SA, et al.: Results of treatment of 255 patients with metastatic renal cell carcinoma who received high-dose recombinant interleukin-2 therapy. J Clin Oncol 13 (3): 688-96, 1995.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_47">Coppin C, Porzsolt F, Awa A, et al.: Immunotherapy for advanced renal cell cancer. Cochrane Database Syst Rev (1): CD001425, 2005.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_48">De Pasquale MD, Pessolano R, Boldrini R, et al.: Continuing response to subsequent treatment lines with tyrosine kinase inhibitors in an adolescent with metastatic renal cell carcinoma. J Pediatr Hematol Oncol 33 (5): e176-9, 2011.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_49">Chowdhury T, Prichard-Jones K, Sebire NJ, et al.: Persistent complete response after single-agent sunitinib treatment in a case of TFE translocation positive relapsed metastatic pediatric renal cell carcinoma. J Pediatr Hematol Oncol 35 (1): e1-3, 2013.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_432_50">Wedekind MF, Ranalli M, Shah N: Clinical efficacy of cabozantinib in two pediatric patients with recurrent renal cell carcinoma. Pediatr Blood Cancer 64 (11): , 2017.</div></li></ol></div></div><div id="CDR0000062789__17"><h2 id="_CDR0000062789__17_">Rhabdoid Tumors of the Kidney</h2><div id="CDR0000062789__885"><h3>General Information About Rhabdoid Tumors of the Kidney</h3><p id="CDR0000062789__373">Rhabdoid tumors are extremely aggressive malignancies that generally occur in infants and young children. The most common locations are the kidney (termed <i>malignant rhabdoid tumors</i>) and the central nervous system (CNS) (atypical teratoid/rhabdoid tumor), although rhabdoid tumors can also arise in most soft tissue sites. (Refer to the PDQ summary on <a href="/books/n/pdqcis/CDR0000587224/">Childhood Central Nervous System Atypical Teratoid/Rhabdoid Tumor Treatment</a> for information about the treatment of CNS disease.) Relapses occur early (median time from diagnosis, 8 months).[<a class="bk_pop" href="#CDR0000062789_rl_17_1">1</a>,<a class="bk_pop" href="#CDR0000062789_rl_17_2">2</a>]</p><p id="CDR0000062789__374">A distinct clinical presentation that suggests a diagnosis of rhabdoid tumor of the kidney includes the following:[<a class="bk_pop" href="#CDR0000062789_rl_17_3">3</a>] </p><ul id="CDR0000062789__1080"><li class="half_rhythm"><div>Fever.</div></li><li class="half_rhythm"><div>Hematuria.</div></li><li class="half_rhythm"><div>Young age (mean age, 11 months).</div></li><li class="half_rhythm"><div>Advanced tumor stage at presentation.</div></li></ul><p id="CDR0000062789__1123">(Refer to the <a href="#CDR0000062789__898">Clinical Features of Wilms Tumor</a> and <a href="#CDR0000062789__900">Diagnostic and Staging Evaluation for Wilms Tumor</a> sections of this summary for more information about the clinical features and diagnostic evaluation of childhood kidney tumors.) </p><p id="CDR0000062789__1081">Approximately two-thirds of patients will present with advanced-stage disease. Bilateral cases have been reported.[<a class="bk_pop" href="#CDR0000062789_rl_17_1">1</a>] Rhabdoid tumors of the kidney tend to metastasize to the lungs and the brain. As many as 10% to 15% of patients with rhabdoid tumors of the kidney also have CNS lesions.[<a class="bk_pop" href="#CDR0000062789_rl_17_4">4</a>] The staging system used for rhabdoid tumor of the kidney is the same system used for Wilms tumor. (Refer to the <a href="#CDR0000062789__23">Stage Information for Wilms Tumor</a> section of this summary for more information.)</p><p id="CDR0000062789__1082">Histologically, the most distinctive features of rhabdoid tumors of the kidney are rather large cells with large vesicular nuclei, a prominent single nucleolus, and in some cells, the presence of globular eosinophilic cytoplasmic inclusions. </p></div><div id="CDR0000062789__1205"><h3>Genomics of Rhabdoid Tumors of the Kidney</h3><div id="CDR0000062789__sm_CDR0000777847_13"><h4>Molecular features of rhabdoid tumors of the kidney</h4><p id="CDR0000062789__sm_CDR0000777847_15">Rhabdoid tumors in all anatomical locations have a common genetic abnormality—loss of function of the <i>SMARCB1 (INI1/SNF5/BAF47)</i> gene located at chromosome 22q11.2. The following text refers to rhabdoid tumors without regard to their primary site. <i>SMARCB1</i> encodes a component of the SWItch/Sucrose Non-Fermentable (SWI/SNF) chromatin remodeling complex that has an important role in controlling gene transcription.[<a class="bk_pop" href="#CDR0000062789_rl_17_5">5</a>,<a class="bk_pop" href="#CDR0000062789_rl_17_6">6</a>] Loss of function occurs by deletions that lead to loss of part or all of the <i>SMARCB1</i> gene and by mutations that are commonly frameshift or nonsense mutations that lead to premature truncation of the SMARCB1 protein.[<a class="bk_pop" href="#CDR0000062789_rl_17_6">6</a>,<a class="bk_pop" href="#CDR0000062789_rl_17_7">7</a>] A small percentage of rhabdoid tumors are caused by alterations in <i>SMARCA4</i>, which is the primary ATPase in the SWI/SNF complex.[<a class="bk_pop" href="#CDR0000062789_rl_17_8">8</a>,<a class="bk_pop" href="#CDR0000062789_rl_17_9">9</a>] Exome sequencing of 35 cases of rhabdoid tumor identified a very low mutation rate, with no genes having recurring mutations other than <i>SMARCB1</i>, which appeared to contribute to tumorigenesis.[<a class="bk_pop" href="#CDR0000062789_rl_17_10">10</a>] </p><p id="CDR0000062789__sm_CDR0000777847_16">Germline mutations of <i>SMARCB1</i> have been documented in patients with one or more primary tumors of the brain and/or kidney, consistent with a genetic predisposition to the development of rhabdoid tumors.[<a class="bk_pop" href="#CDR0000062789_rl_17_11">11</a>,<a class="bk_pop" href="#CDR0000062789_rl_17_12">12</a>] Approximately one-third of patients with rhabdoid tumors have germline <i>SMARCB1</i> alterations.[<a class="bk_pop" href="#CDR0000062789_rl_17_6">6</a>,<a class="bk_pop" href="#CDR0000062789_rl_17_13">13</a>] In most cases, the mutations are de novo and not inherited. The median age at diagnosis of children with rhabdoid tumors and a germline mutation or deletion is younger (6 months) than that of children with apparently sporadic disease (18 months).[<a class="bk_pop" href="#CDR0000062789_rl_17_14">14</a>] Early-onset, multifocal disease and familial cases with the presence of <i>SMARCB1</i> strongly support the possibility of rhabdoid tumor predisposition syndrome, type 1.</p><p id="CDR0000062789__sm_CDR0000777847_961">Thirty-five patients (N = 100) with rhabdoid tumors of the brain, kidney, or soft tissues were found to have a germline <i>SMARCB1</i> abnormality. These abnormalities included point and frameshift mutations, intragenic deletions and duplications, and larger deletions. Nine cases demonstrated parent-to-child transmission of a mutated copy of <i>SMARCB1</i>. In eight of the nine cases, one or more family members were also diagnosed with rhabdoid tumor or schwannoma; two of the eight families presented with multiple affected children, consistent with gonadal mosaicism.[<a class="bk_pop" href="#CDR0000062789_rl_17_6">6</a>] It appears that patients with germline mutations may have the worst prognosis.[<a class="bk_pop" href="#CDR0000062789_rl_17_15">15</a>,<a class="bk_pop" href="#CDR0000062789_rl_17_16">16</a>]</p><p id="CDR0000062789__sm_CDR0000777847_960">Two cases of inactivating mutations in the <i>SMARCA4</i> gene have been found in three children from two unrelated families, establishing the phenotypically similar syndrome now known as rhabdoid tumor predisposition syndrome, type 2.[<a class="bk_pop" href="#CDR0000062789_rl_17_8">8</a>,<a class="bk_pop" href="#CDR0000062789_rl_17_9">9</a>,<a class="bk_pop" href="#CDR0000062789_rl_17_17">17</a>,<a class="bk_pop" href="#CDR0000062789_rl_17_17">17</a>] In these cases, <i>SMARCA4</i> behaves as a classical tumor suppressor, with one deleterious mutation inherited in the germline and the other acquired in the tumor. Another report describes an autosomal dominant pattern of inheritance discovered through an exome sequencing project.[<a class="bk_pop" href="#CDR0000062789_rl_17_18">18</a>] </p></div></div><div id="CDR0000062789__1105"><h3>Genetic Testing and Surveillance of Rhabdoid Tumors of the Kidney</h3><p id="CDR0000062789__1106">Germline analysis is suggested for individuals of all ages with rhabdoid tumors. Genetic counseling is also part of the treatment plan, given the low-but-actual risk of familial recurrence. In cases of mutations, parental screening should be considered, although such screening carries a low probability of positivity. Prenatal diagnosis can be performed in situations in which a specific <i>SMARCB1</i> mutation or deletion has been documented in the family.[<a class="bk_pop" href="#CDR0000062789_rl_17_6">6</a>]</p><p id="CDR0000062789__1107">To date, there is little evidence regarding the effectiveness of surveillance for patients with rhabdoid tumor predisposition syndrome, type 1 caused by loss-of-function germline <i>SMARCB1</i> mutations. However, because of the aggressive nature of the tumors with significant lethality and young age of onset in <i>SMARCB1</i> carriers with truncating mutations, consensus recommendations have been developed. These recommendations were developed by a group of pediatric cancer genetic experts (including oncologists, radiologists, and geneticists). They have not been formally studied to confirm the benefit of monitoring patients with germline <i>SMARCB1</i> mutations. Given the potential survival benefit of surgically resectable disease, it is postulated that early detection might improve overall survival (OS).[<a class="bk_pop" href="#CDR0000062789_rl_17_19">19</a>-<a class="bk_pop" href="#CDR0000062789_rl_17_21">21</a>]</p><p id="CDR0000062789__1286">Surveillance for patients with germline <i>SMARCB1</i> mutations includes the following:</p><ul id="CDR0000062789__1108"><li class="half_rhythm"><div>Brain magnetic resonance imaging (MRI) every 3 months from birth (or diagnosis) until age 5 years.</div></li><li class="half_rhythm"><div> Abdominal ultrasonography with a focus on the kidneys every 3 months.</div></li></ul></div><div id="CDR0000062789__1287"><h3>Prognosis and Prognostic Factors for Rhabdoid Tumors of the Kidney</h3><p id="CDR0000062789__1288">Patients with rhabdoid tumors of the kidney have a poor prognosis.
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In a review of 142 patients from the National Wilms Tumor Studies (NWTS) (NWTS-1, NWTS-2, NWTS-3, NWTS-4, and <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5 [COG-Q9401/NCT00002611]</a>), age and stage were identified as important prognostic factors:[<a class="bk_pop" href="#CDR0000062789_rl_17_4">4</a>]</p><ul id="CDR0000062789__1289"><li class="half_rhythm"><div><b>Age at diagnosis.</b> Infants younger than 6 months at diagnosis demonstrated a 4-year OS rate of 9%, whereas the OS rate in patients aged 2 years and older was 41% (highly significant).</div></li><li class="half_rhythm"><div><b>Stage of disease.</b> Patients with stage I and stage II disease had an OS rate of 42%; higher stage was associated with a 16% OS rate.</div></li><li class="half_rhythm"><div><b>Presence of a CNS lesion.</b> All but one patient with a CNS lesion (n = 32) died.</div></li></ul></div><div id="CDR0000062789__103"><h3>Treatment of Rhabdoid Tumor of the Kidney</h3><p id="CDR0000062789__378">Because of the relative rarity of this tumor, all patients with rhabdoid tumor of the kidney should be considered for entry into a clinical trial. Treatment planning by a multidisciplinary team of cancer specialists (pediatric surgeon or pediatric urologist, pediatric radiation oncologist, and pediatric oncologist) with experience treating renal tumors is required to determine and implement optimal treatment.</p><p id="CDR0000062789__819">There are no standard treatment options for rhabdoid tumor of the kidney.[<a class="bk_pop" href="#CDR0000062789_rl_17_22">22</a>]</p><p id="CDR0000062789__1290">The following results have been observed in studies of rhabdoid tumor of the kidney:</p><ol id="CDR0000062789__1301"><li class="half_rhythm"><div>On the basis of a retrospective comparison of tumor response to preoperative treatment with vincristine/dactinomycin versus vincristine/dactinomycin/doxorubicin, doxorubicin is considered an active drug in malignant rhabdoid tumor of the kidney.[<a class="bk_pop" href="#CDR0000062789_rl_17_23">23</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000587991/" class="def">Level of evidence: 3iiiDiv</a>]</div></li><li class="half_rhythm"><div>The <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5</a> trial closed the arm for patients with rhabdoid tumor who were treated with cyclophosphamide, etoposide, and carboplatin because poor outcomes were observed. Combinations of etoposide and cisplatin;
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etoposide and ifosfamide; and ifosfamide, carboplatin, and etoposide (ICE chemotherapy) have been used.[<a class="bk_pop" href="#CDR0000062789_rl_17_24">24</a>,<a class="bk_pop" href="#CDR0000062789_rl_17_25">25</a>] </div></li><li class="half_rhythm"><div>Treatment with high-dose alkylator therapy followed by consolidation with high-dose chemotherapy and, in some cases, autologous stem cell transplant after achieving a radiographic remission has resulted in some long-term survival (5 of 13 patients). None of the patients with unresectable primary tumors survived in this small series (N = 21).[<a class="bk_pop" href="#CDR0000062789_rl_17_26">26</a>]</div></li><li class="half_rhythm"><div>A retrospective analysis of 58 patients with malignant rhabdoid tumor of the kidney from the International Society of Pediatric Oncology (SIOP), Gesellschaft für Pädiatrische Onkologie und Hämatologie (GPOH), and European Rhabdoid Tumor Registry was performed.[<a class="bk_pop" href="#CDR0000062789_rl_17_27">27</a>]<ul id="CDR0000062789__1839"><li class="half_rhythm"><div>For the entire group, the 2-year event-free survival (EFS) rate was 37%, and the OS rate was 38%.</div></li><li class="half_rhythm"><div>Patients with multifocal involvement (n = 12) had significantly inferior survival than did patients with pulmonary or mediastinal metastases or local disease.</div></li><li class="half_rhythm"><div>Patients who underwent upfront chemotherapy had a lower, but not statistically significant, 2-year EFS than did patients who underwent immediate surgical resection.</div></li><li class="half_rhythm"><div>Younger age (<12 months) and local stage III disease were associated with significantly inferior survival than were stage I and stage II disease.</div></li><li class="half_rhythm"><div>No difference was seen in 2-year EFS for patients without progression within 90 days consolidated by high-dose stem cell transplantation (SCT) (n = 10) compared with patients without consolidation by SCT (n = 21).</div></li></ul></div></li></ol></div><div id="CDR0000062789__1236"><h3>Treatment Options Under Clinical Evaluation for Rhabdoid Tumors of the Kidney</h3><p id="CDR0000062789__1834">Information about National Cancer Institute (NCI)–supported clinical trials can be found on the <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NCI website</a>. For information about clinical trials sponsored by other organizations, refer to the <a href="https://clinicaltrials.gov/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">ClinicalTrials.gov website</a>.</p><p id="CDR0000062789__1237">The following are examples of national and/or institutional clinical trials that are currently being conducted:</p><ul id="CDR0000062789__1238"><li class="half_rhythm"><div class="half_rhythm"><b><a href="https://www.cancer.gov/clinicaltrials/NCT03155620" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">APEC1621 (NCT03155620)</a></b> (Pediatric MATCH: Targeted Therapy Directed by Genetic Testing in Treating Pediatric Patients with Relapsed or Refractory Advanced Solid Tumors, Non-Hodgkin Lymphomas, or Histiocytic Disorders)<b>:</b> NCI–Children's Oncology Group Pediatric Molecular Analysis for Therapeutic Choice (MATCH), referred to as Pediatric MATCH, will match targeted agents with specific molecular changes identified using a next-generation sequencing targeted assay of more than 4,000 different mutations across more than 160 genes in refractory and recurrent solid tumors. Children and adolescents aged 1 to 21 years are eligible for the trial.</div><div class="half_rhythm">Tumor tissue from progressive or recurrent disease must be available for molecular characterization. Patients with tumors that have molecular variants addressed by treatment arms included in the trial will be offered treatment on Pediatric MATCH. Additional information can be obtained on the <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/nci-supported/pediatric-match" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NCI website</a> and <a href="https://clinicaltrials.gov/ct2/show/NCT03155620" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">ClinicalTrials.gov website</a>.
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</div></li><li class="half_rhythm"><div class="half_rhythm"><b><a href="https://www.cancer.gov/clinicaltrials/NCT02601937" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NCT02601937</a></b> (A Phase 1 Study of the EZH2 Inhibitor Tazemetostat in Pediatric Subjects With Relapsed or Refractory INI1-Negative Tumors or Synovial Sarcoma)<b>:</b> Patients with <i>INI1</i>-negative tumors are eligible for targeted treatment with an EZH2 inhibitor. This is a phase I, open-label, dose-escalation, and dose-expansion study with a twice-daily oral dose of tazemetostat.</div></li></ul></div><div id="CDR0000062789__TrialSearch_17_sid_4"><h3>Current Clinical Trials</h3><p id="CDR0000062789__TrialSearch_17_22">Use our <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/advanced-search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">advanced clinical trial search</a> to find NCI-supported cancer clinical trials that are now enrolling patients. The search can be narrowed by location of the trial, type of treatment, name of the drug, and other criteria. <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">General information</a> about clinical trials is also available.</p></div><div id="CDR0000062789_rl_17"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_17_1">van den Heuvel-Eibrink MM, van Tinteren H, Rehorst H, et al.: Malignant rhabdoid tumours of the kidney (MRTKs), registered on recent SIOP protocols from 1993 to 2005: a report of the SIOP renal tumour study group. Pediatr Blood Cancer 56 (5): 733-7, 2011. [<a href="https://pubmed.ncbi.nlm.nih.gov/21370404" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 21370404</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_2">Reinhard H, Reinert J, Beier R, et al.: Rhabdoid tumors in children: prognostic factors in 70 patients diagnosed in Germany. Oncol Rep 19 (3): 819-23, 2008. [<a href="https://pubmed.ncbi.nlm.nih.gov/18288421" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 18288421</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_3">Amar AM, Tomlinson G, Green DM, et al.: Clinical presentation of rhabdoid tumors of the kidney. J Pediatr Hematol Oncol 23 (2): 105-8, 2001. [<a href="https://pubmed.ncbi.nlm.nih.gov/11216700" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 11216700</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_4">Tomlinson GE, Breslow NE, Dome J, et al.: Rhabdoid tumor of the kidney in the National Wilms' Tumor Study: age at diagnosis as a prognostic factor. J Clin Oncol 23 (30): 7641-5, 2005. [<a href="https://pubmed.ncbi.nlm.nih.gov/16234525" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 16234525</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_5">Imbalzano AN, Jones SN: Snf5 tumor suppressor couples chromatin remodeling, checkpoint control, and chromosomal stability. Cancer Cell 7 (4): 294-5, 2005. [<a href="https://pubmed.ncbi.nlm.nih.gov/15837618" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 15837618</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_6">Eaton KW, Tooke LS, Wainwright LM, et al.: Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors. Pediatr Blood Cancer 56 (1): 7-15, 2011. [<a href="/pmc/articles/PMC3086793/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC3086793</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/21108436" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 21108436</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_7">Versteege I, Sévenet N, Lange J, et al.: Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer. Nature 394 (6689): 203-6, 1998. [<a href="https://pubmed.ncbi.nlm.nih.gov/9671307" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 9671307</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_8">Schneppenheim R, Frühwald MC, Gesk S, et al.: Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome. Am J Hum Genet 86 (2): 279-84, 2010. [<a href="/pmc/articles/PMC2820190/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC2820190</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/20137775" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 20137775</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_9">Hasselblatt M, Gesk S, Oyen F, et al.: Nonsense mutation and inactivation of SMARCA4 (BRG1) in an atypical teratoid/rhabdoid tumor showing retained SMARCB1 (INI1) expression. Am J Surg Pathol 35 (6): 933-5, 2011. [<a href="https://pubmed.ncbi.nlm.nih.gov/21566516" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 21566516</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_10">Lee RS, Stewart C, Carter SL, et al.: A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers. J Clin Invest 122 (8): 2983-8, 2012. [<a href="/pmc/articles/PMC3408754/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC3408754</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/22797305" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 22797305</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_11">Biegel JA, Zhou JY, Rorke LB, et al.: Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors. Cancer Res 59 (1): 74-9, 1999. [<a href="https://pubmed.ncbi.nlm.nih.gov/9892189" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 9892189</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_12">Biegel JA: Molecular genetics of atypical teratoid/rhabdoid tumor. Neurosurg Focus 20 (1): E11, 2006. [<a href="https://pubmed.ncbi.nlm.nih.gov/16459991" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 16459991</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_13">Bourdeaut F, Lequin D, Brugières L, et al.: Frequent hSNF5/INI1 germline mutations in patients with rhabdoid tumor. Clin Cancer Res 17 (1): 31-8, 2011. [<a href="https://pubmed.ncbi.nlm.nih.gov/21208904" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 21208904</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_14">Geller JI, Roth JJ, Biegel JA: Biology and Treatment of Rhabdoid Tumor. Crit Rev Oncog 20 (3-4): 199-216, 2015. [<a href="/pmc/articles/PMC6087667/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC6087667</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/26349416" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 26349416</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_15">Janson K, Nedzi LA, David O, et al.: Predisposition to atypical teratoid/rhabdoid tumor due to an inherited INI1 mutation. Pediatr Blood Cancer 47 (3): 279-84, 2006. [<a href="https://pubmed.ncbi.nlm.nih.gov/16261613" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 16261613</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_16">Sévenet N, Sheridan E, Amram D, et al.: Constitutional mutations of the hSNF5/INI1 gene predispose to a variety of cancers. Am J Hum Genet 65 (5): 1342-8, 1999. [<a href="/pmc/articles/PMC1288286/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC1288286</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/10521299" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 10521299</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_17">Hasselblatt M, Nagel I, Oyen F, et al.: SMARCA4-mutated atypical teratoid/rhabdoid tumors are associated with inherited germline alterations and poor prognosis. Acta Neuropathol 128 (3): 453-6, 2014. [<a href="https://pubmed.ncbi.nlm.nih.gov/25060813" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 25060813</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_18">Witkowski L, Lalonde E, Zhang J, et al.: Familial rhabdoid tumour 'avant la lettre'--from pathology review to exome sequencing and back again. J Pathol 231 (1): 35-43, 2013. [<a href="https://pubmed.ncbi.nlm.nih.gov/23775540" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 23775540</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_19">Teplick A, Kowalski M, Biegel JA, et al.: Educational paper: screening in cancer predisposition syndromes: guidelines for the general pediatrician. Eur J Pediatr 170 (3): 285-94, 2011. [<a href="/pmc/articles/PMC3086787/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC3086787</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/21210147" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 21210147</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_20">Mitchell SG, Pencheva B, Porter CC: Germline Genetics and Childhood Cancer: Emerging Cancer Predisposition Syndromes and Psychosocial Impacts. Curr Oncol Rep 21 (10): 85, 2019. [<a href="https://pubmed.ncbi.nlm.nih.gov/31414239" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 31414239</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_21">Foulkes WD, Kamihara J, Evans DGR, et al.: Cancer Surveillance in Gorlin Syndrome and Rhabdoid Tumor Predisposition Syndrome. Clin Cancer Res 23 (12): e62-e67, 2017. [<a href="/pmc/articles/PMC7309678/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC7309678</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/28620006" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 28620006</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_22">Ahmed HU, Arya M, Levitt G, et al.: Part II: Treatment of primary malignant non-Wilms' renal tumours in children. Lancet Oncol 8 (9): 842-8, 2007. [<a href="https://pubmed.ncbi.nlm.nih.gov/17765193" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 17765193</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_23">Furtwängler R, Nourkami-Tutdibi N, Leuschner I, et al.: Malignant rhabdoid tumor of the kidney: significantly improved response to pre-operative treatment intensified with doxorubicin. Cancer Genet 207 (9): 434-6, 2014. [<a href="https://pubmed.ncbi.nlm.nih.gov/25242089" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 25242089</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_24">Waldron PE, Rodgers BM, Kelly MD, et al.: Successful treatment of a patient with stage IV rhabdoid tumor of the kidney: case report and review. J Pediatr Hematol Oncol 21 (1): 53-7, 1999 Jan-Feb. [<a href="https://pubmed.ncbi.nlm.nih.gov/10029814" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 10029814</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_25">Wagner L, Hill DA, Fuller C, et al.: Treatment of metastatic rhabdoid tumor of the kidney. J Pediatr Hematol Oncol 24 (5): 385-8, 2002 Jun-Jul. [<a href="https://pubmed.ncbi.nlm.nih.gov/12142788" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 12142788</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_26">Venkatramani R, Shoureshi P, Malvar J, et al.: High dose alkylator therapy for extracranial malignant rhabdoid tumors in children. Pediatr Blood Cancer 61 (8): 1357-61, 2014. [<a href="https://pubmed.ncbi.nlm.nih.gov/24789740" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 24789740</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_17_27">Furtwängler R, Kager L, Melchior P, et al.: High-dose treatment for malignant rhabdoid tumor of the kidney: No evidence for improved survival-The Gesellschaft für Pädiatrische Onkologie und Hämatologie (GPOH) experience. Pediatr Blood Cancer 65 (1): , 2018. [<a href="https://pubmed.ncbi.nlm.nih.gov/28843054" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 28843054</span></a>]</div></li></ol></div></div><div id="CDR0000062789__10"><h2 id="_CDR0000062789__10_">Clear Cell Sarcoma of the Kidney</h2><div id="CDR0000062789__887"><h3>General Information About Clear Cell Sarcoma of the Kidney</h3><p id="CDR0000062789__2011">Clear cell sarcoma of the kidney is an uncommon renal tumor that comprises approximately 5% of all primary renal malignancies in children, accounts for approximately 20 new cases per year in the United States, and is observed most often before age 3 years.[<a class="bk_pop" href="#CDR0000062789_rl_10_1">1</a>] </p><p id="CDR0000062789__780">Clear cell sarcoma of the kidney is not a Wilms tumor variant, but it
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is an important primary renal tumor associated with a higher rate
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of relapse and death than is favorable histology (FH) Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_10_1">1</a>] The classic pattern of clear cell sarcoma of the kidney is defined by nests or cords of cells
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separated by regularly spaced fibrovascular septa. In addition to
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pulmonary metastases, clear cell sarcoma also spreads to bone, brain, and soft
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tissue.[<a class="bk_pop" href="#CDR0000062789_rl_10_1">1</a>] (Refer to the <a href="#CDR0000062789__898">Clinical Features of Wilms Tumor</a> and <a href="#CDR0000062789__900">Diagnostic and Staging Evaluation for Wilms Tumor</a> sections of this summary for more information about the clinical features and diagnostic evaluation of childhood kidney tumors.)</p><p id="CDR0000062789__953">Younger age and stage IV disease have been identified as adverse prognostic factors for event-free survival (EFS).[<a class="bk_pop" href="#CDR0000062789_rl_10_2">2</a>]</p><p id="CDR0000062789__782">Historically, relapses have occurred up to 14 years after the completion of chemotherapy; however, with current therapy, relapses after 3 years are uncommon.[<a class="bk_pop" href="#CDR0000062789_rl_10_3">3</a>] The brain is a frequent site of recurrent disease, suggesting that it is a sanctuary site for cells that are protected from the intensive chemotherapy that patients receive.[<a class="bk_pop" href="#CDR0000062789_rl_10_2">2</a>-<a class="bk_pop" href="#CDR0000062789_rl_10_5">5</a>] An awareness of the clinical signs of recurrent disease in the brain is important during regular follow-up.
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There are no standard recommendations for the frequency of brain imaging during follow-up. </p></div><div id="CDR0000062789__1206"><h3>Genomics of Clear Cell Sarcoma of the Kidney</h3><div id="CDR0000062789__sm_CDR0000777848_13"><h4>Molecular features of clear cell sarcoma of the kidney</h4><p id="CDR0000062789__sm_CDR0000777848_15">The molecular background of clear cell sarcoma of the kidney is poorly understood because of its rarity and lack of experimental models. However, several molecular features of clear cell sarcoma of the kidney have been described, including the following:</p><ul id="CDR0000062789__sm_CDR0000777848_16"><li class="half_rhythm"><div>Internal tandem duplications in exon 15 of the <i>BCOR</i> gene (BCL6 corepressor) have been reported in 90% of cases of clear cell sarcoma of the kidney, with a smaller subset harboring <i>YWHAE-NUTM2B/E</i> or <i>BCOR-CCNB3</i> gene fusions.[<a class="bk_pop" href="#CDR0000062789_rl_10_6">6</a>-<a class="bk_pop" href="#CDR0000062789_rl_10_11">11</a>] All of these genetic abnormalities result in a transcriptional signature characterized by high BCOR mRNA expression.[<a class="bk_pop" href="#CDR0000062789_rl_10_12">12</a>]</div></li><li class="half_rhythm"><div>Diffuse strong immunoreactivity for <i>BCOR</i> is highly sensitive and specific for the diagnosis of clear cell sarcoma of the kidney. In a series of 79 neoplasms—including Wilms tumors, congenital mesoblastic nephromas, clear cell sarcoma of the kidney, metanephric stromal tumors, rhabdoid tumors of the kidney, renal primitive neuroectodermal tumor (PNET), and sclerosing epithelioid fibrosarcomas—all of the clear cell sarcomas of the kidney samples that were tested demonstrated diffuse, strong nuclear labeling for <i>BCOR</i>. Most of the other pediatric renal neoplasms were completely negative for <i>BCOR</i>.[<a class="bk_pop" href="#CDR0000062789_rl_10_13">13</a>]</div></li></ul></div></div><div id="CDR0000062789__99"><h3>Treatment of Clear Cell Sarcoma of the Kidney</h3><p id="CDR0000062789__377">Because of the relative rarity of this tumor, all patients with clear cell sarcoma of the kidney should be considered for entry into a clinical trial. Treatment planning by a multidisciplinary team of cancer specialists (pediatric surgeon or pediatric urologist, pediatric radiation oncologist, and pediatric oncologist) with experience treating renal tumors is required to determine and implement optimal treatment.</p><p id="CDR0000062789__824">The approach for treating clear cell sarcoma of the kidney is different from the approach for treating
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Wilms tumor because the overall survival (OS) of children with clear cell sarcoma of the kidney remains lower than that for patients with FH Wilms tumor. All patients undergo postoperative radiation to the tumor bed and receive doxorubicin as part of their chemotherapy regimen.</p><p id="CDR0000062789__825">The standard treatment option for clear cell sarcoma of the kidney is the following:</p><ol id="CDR0000062789__826"><li class="half_rhythm"><div><a href="#CDR0000062789__1061">Surgery, chemotherapy, and radiation therapy</a>.</div></li></ol><div id="CDR0000062789__1061"><h4>Surgery, chemotherapy, and radiation therapy</h4><p id="CDR0000062789__827">Evidence (surgery, chemotherapy, and radiation therapy):</p><ol id="CDR0000062789__828"><li class="half_rhythm"><div> In the National Wilms Tumor Study (NWTS)-3 trial (NWTS-3), the addition of doxorubicin to the combination of vincristine,
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dactinomycin, and radiation therapy resulted in an improvement in disease-free
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survival for patients with clear cell sarcoma of the kidney.[<a class="bk_pop" href="#CDR0000062789_rl_10_1">1</a>]</div></li><li class="half_rhythm"><div>The NWTS-4 trial used regimen DD-4A, which consisted of vincristine, dactinomycin, and doxorubicin for 15 months, and radiation therapy.[<a class="bk_pop" href="#CDR0000062789_rl_10_14">14</a>]<ul id="CDR0000062789__817"><li class="half_rhythm"><div>Patients who were treated with vincristine, doxorubicin, and dactinomycin for 15 months had an improved relapse-free survival rate compared with patients who were treated for 6 months (88% vs. 61% at 8 years).</div></li></ul></div></li><li class="half_rhythm"><div>In the <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5 (COG-Q9401/NCT00002611)</a> trial, children with stages
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I to IV clear cell sarcoma of the kidney were treated with a new
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chemotherapeutic regimen combining vincristine, doxorubicin, cyclophosphamide,
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and etoposide in an attempt to further improve the survival of these high-risk
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groups. All patients received radiation therapy to the tumor bed.[<a class="bk_pop" href="#CDR0000062789_rl_10_3">3</a>] <ul id="CDR0000062789__818"><li class="half_rhythm"><div>With this treatment, the 5-year EFS rate was 79%, and the OS rate was 90%.</div></li><li class="half_rhythm"><div>Stage I patients had 5-year EFS and OS rates of 100%.</div></li><li class="half_rhythm"><div>Stage II patients had a 5-year EFS rate of 88% and a 5-year OS rate of 98%.</div></li><li class="half_rhythm"><div>Stage III patients had a 5-year EFS rate of 73% and a 5-year OS rate of 89%.</div></li><li class="half_rhythm"><div>Stage IV patients had a 5-year EFS rate of 29% and a 5-year OS rate of 36%.</div></li></ul></div></li><li class="half_rhythm"><div>A review of patients with stage I clear cell sarcoma of the kidney treated on the NWTS-1, NWTS-2, NWTS-3, NWTS-4, and <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5</a> trials showed an excellent OS rate of 100% with a wide variety of chemotherapy and radiation therapy regimens.[<a class="bk_pop" href="#CDR0000062789_rl_10_15">15</a>]</div></li></ol><p id="CDR0000062789__1870">(Refer to the <a href="#CDR0000062789__598">Treatment of Recurrent Clear Cell Sarcoma of the Kidney</a> section of this summary for information about recurrent disease.)</p></div></div><div id="CDR0000062789__TrialSearch_10_sid_5"><h3>Current Clinical Trials</h3><p id="CDR0000062789__TrialSearch_10_22">Use our <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/advanced-search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">advanced clinical trial search</a> to find NCI-supported cancer clinical trials that are now enrolling patients. The search can be narrowed by location of the trial, type of treatment, name of the drug, and other criteria. <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">General information</a> about clinical trials is also available.</p></div><div id="CDR0000062789_rl_10"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_10_1">Argani P, Perlman EJ, Breslow NE, et al.: Clear cell sarcoma of the kidney: a review of 351 cases from the National Wilms Tumor Study Group Pathology Center. Am J Surg Pathol 24 (1): 4-18, 2000. [<a href="https://pubmed.ncbi.nlm.nih.gov/10632483" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 10632483</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_10_2">Furtwängler R, Gooskens SL, van Tinteren H, et al.: Clear cell sarcomas of the kidney registered on International Society of Pediatric Oncology (SIOP) 93-01 and SIOP 2001 protocols: a report of the SIOP Renal Tumour Study Group. Eur J Cancer 49 (16): 3497-506, 2013. [<a href="https://pubmed.ncbi.nlm.nih.gov/23880476" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 23880476</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_10_3">Seibel NL, Chi YY, Perlman EJ, et al.: Impact of cyclophosphamide and etoposide on outcome of clear cell sarcoma of the kidney treated on the National Wilms Tumor Study-5 (NWTS-5). Pediatr Blood Cancer 66 (1): e27450, 2019. [<a href="/pmc/articles/PMC6249042/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC6249042</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/30255545" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 30255545</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_10_4">Radulescu VC, Gerrard M, Moertel C, et al.: Treatment of recurrent clear cell sarcoma of the kidney with brain metastasis. Pediatr Blood Cancer 50 (2): 246-9, 2008. [<a href="https://pubmed.ncbi.nlm.nih.gov/17226850" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 17226850</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_10_5">Gooskens SL, Furtwängler R, Spreafico F, et al.: Treatment and outcome of patients with relapsed clear cell sarcoma of the kidney: a combined SIOP and AIEOP study. Br J Cancer 111 (2): 227-33, 2014. [<a href="/pmc/articles/PMC4102945/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC4102945</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/24937667" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 24937667</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_10_6">Ueno-Yokohata H, Okita H, Nakasato K, et al.: Consistent in-frame internal tandem duplications of BCOR characterize clear cell sarcoma of the kidney. Nat Genet 47 (8): 861-3, 2015. [<a href="https://pubmed.ncbi.nlm.nih.gov/26098867" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 26098867</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_10_7">Argani P, Kao YC, Zhang L, et al.: Primary Renal Sarcomas With BCOR-CCNB3 Gene Fusion: A Report of 2 Cases Showing Histologic Overlap With Clear Cell Sarcoma of Kidney, Suggesting Further Link Between BCOR-related Sarcomas of the Kidney and Soft Tissues. Am J Surg Pathol 41 (12): 1702-1712, 2017. [<a href="/pmc/articles/PMC5680139/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC5680139</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/28817404" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 28817404</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_10_8">Karlsson J, Valind A, Gisselsson D: BCOR internal tandem duplication and YWHAE-NUTM2B/E fusion are mutually exclusive events in clear cell sarcoma of the kidney. Genes Chromosomes Cancer 55 (2): 120-3, 2016. [<a href="https://pubmed.ncbi.nlm.nih.gov/26493387" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 26493387</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_10_9">Astolfi A, Melchionda F, Perotti D, et al.: Whole transcriptome sequencing identifies BCOR internal tandem duplication as a common feature of clear cell sarcoma of the kidney. Oncotarget 6 (38): 40934-9, 2015. [<a href="/pmc/articles/PMC4747379/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC4747379</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/26516930" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 26516930</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_10_10">Roy A, Kumar V, Zorman B, et al.: Recurrent internal tandem duplications of BCOR in clear cell sarcoma of the kidney. Nat Commun 6: 8891, 2015. [<a href="/pmc/articles/PMC4660214/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC4660214</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/26573325" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 26573325</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_10_11">Wong MK, Ng CCY, Kuick CH, et al.: Clear cell sarcomas of the kidney are characterised by BCOR gene abnormalities, including exon 15 internal tandem duplications and BCOR-CCNB3 gene fusion. Histopathology 72 (2): 320-329, 2018. [<a href="https://pubmed.ncbi.nlm.nih.gov/28833375" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 28833375</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_10_12">Kao YC, Sung YS, Zhang L, et al.: Recurrent BCOR Internal Tandem Duplication and YWHAE-NUTM2B Fusions in Soft Tissue Undifferentiated Round Cell Sarcoma of Infancy: Overlapping Genetic Features With Clear Cell Sarcoma of Kidney. Am J Surg Pathol 40 (8): 1009-20, 2016. [<a href="/pmc/articles/PMC4942366/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC4942366</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/26945340" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 26945340</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_10_13">Argani P, Pawel B, Szabo S, et al.: Diffuse Strong BCOR Immunoreactivity Is a Sensitive and Specific Marker for Clear Cell Sarcoma of the Kidney (CCSK) in Pediatric Renal Neoplasia. Am J Surg Pathol 42 (8): 1128-1131, 2018. [<a href="/pmc/articles/PMC6041176/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC6041176</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/29851702" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 29851702</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_10_14">Seibel NL, Li S, Breslow NE, et al.: Effect of duration of treatment on treatment outcome for patients with clear-cell sarcoma of the kidney: a report from the National Wilms' Tumor Study Group. J Clin Oncol 22 (3): 468-73, 2004. [<a href="https://pubmed.ncbi.nlm.nih.gov/14752069" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 14752069</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_10_15">Kalapurakal JA, Perlman EJ, Seibel NL, et al.: Outcomes of patients with revised stage I clear cell sarcoma of kidney treated in National Wilms Tumor Studies 1-5. Int J Radiat Oncol Biol Phys 85 (2): 428-31, 2013. [<a href="https://pubmed.ncbi.nlm.nih.gov/22658515" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 22658515</span></a>]</div></li></ol></div></div><div id="CDR0000062789__429"><h2 id="_CDR0000062789__429_">Congenital Mesoblastic Nephroma</h2><div id="CDR0000062789__888"><h3>General Information About Congenital Mesoblastic Nephroma</h3><p id="CDR0000062789__430">Mesoblastic nephroma comprises about 5% of childhood kidney tumors, and more than 90% of cases appear within the first year of life. More than 15% of the cases are detected prenatally.[<a class="bk_pop" href="#CDR0000062789_rl_429_1">1</a>] It is the most common kidney tumor found in infants younger than 6 months, with a median age at diagnosis of 1 to 2 months.[<a class="bk_pop" href="#CDR0000062789_rl_429_2">2</a>] Twice as many males as females are diagnosed. The diagnosis should be questioned when applied to individuals older than 2 years.[<a class="bk_pop" href="#CDR0000062789_rl_429_1">1</a>] </p><p id="CDR0000062789__1037">When patients are diagnosed in the first 7 months of life, the 5-year event-free survival rate is 94%, and the overall survival (OS) rate is 96%.[<a class="bk_pop" href="#CDR0000062789_rl_429_3">3</a>] In a report from the United Kingdom of 50 children with mesoblastic nephroma studied on clinical trials and 80 cases from the national registry in the same time period, there were no deaths.[<a class="bk_pop" href="#CDR0000062789_rl_429_1">1</a>] However, in a comprehensive review of the literature, 12 deaths were reported; of these 12 deaths, 7 were from surgical complications in infants.[<a class="bk_pop" href="#CDR0000062789_rl_429_4">4</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335155/" class="def">Level of evidence: 3iiiDii</a>]</p><p id="CDR0000062789__431">Grossly, mesoblastic nephromas appear as solitary, unilateral masses indistinguishable from nephroblastoma. Microscopically, they consist of spindled mesenchymal cells. Mesoblastic nephroma can be divided into the following three histologic subtypes:</p><ul id="CDR0000062789__1038"><li class="half_rhythm"><div><b>Classic.</b>[<a class="bk_pop" href="#CDR0000062789_rl_429_5">5</a>]</div></li><li class="half_rhythm"><div><b>Cellular.</b> The cellular subtype is identical to infantile fibrosarcoma.[<a class="bk_pop" href="#CDR0000062789_rl_429_6">6</a>]</div></li><li class="half_rhythm"><div><b>Mixed.</b> The mixed subtype (<10%) is a mixture of classic and cellular patterns.[<a class="bk_pop" href="#CDR0000062789_rl_429_7">7</a>]</div></li></ul><p id="CDR0000062789__1307">A frequent genetic alteration is the translocation t(12;15)(q13;q25), resulting in a fusion of the <i>ETV6</i> and <i>NTRK3</i> genes on 15p15 that occurs almost exclusively in the cellular type of mesoblastic nephroma. In a cohort of 79 mesoblastic nephromas analyzed for the translocation, all classical (n = 38) and mixed (n = 12) mesoblastic nephromas were translocation negative.[<a class="bk_pop" href="#CDR0000062789_rl_429_8">8</a>] The same translocation was initially described in infantile fibrosarcoma, and besides the similar morphologic appearance, cases of cellular mesoblastic nephroma and infantile fibrosarcoma share other genetic changes such as gains of chromosome 11.[<a class="bk_pop" href="#CDR0000062789_rl_429_9">9</a>]</p><p id="CDR0000062789__1039">The risk of recurrence for patients with mesoblastic nephroma is closely associated with the presence of a cellular subtype and with stage III disease.[<a class="bk_pop" href="#CDR0000062789_rl_429_5">5</a>] In an International Society of Pediatric Oncology (SIOP) series of 79 patients with congenital mesoblastic nephromas, patients within the cellular subgroup who had translocation-positive tumors had a significantly superior relapse-free survival (RFS) rate when compared with patients who did not have the gene fusion (100% vs. 73%, respectively).[<a class="bk_pop" href="#CDR0000062789_rl_429_8">8</a>]</p><p id="CDR0000062789__963">(Refer to the <a href="#CDR0000062789__898">Clinical Features of Wilms Tumor</a> and <a href="#CDR0000062789__900">Diagnostic and Staging Evaluation for Wilms Tumor</a> sections of this summary for more information about the clinical features and diagnostic evaluation of childhood kidney tumors.)</p></div><div id="CDR0000062789__283"><h3>Treatment of Congenital Mesoblastic Nephroma</h3><p id="CDR0000062789__1308">The OS of patients with congenital mesoblastic nephroma is excellent; however, reported causes of death in about one-half of the cases are treatment related, and most of these patients were very young (median age, <1 year).[<a class="bk_pop" href="#CDR0000062789_rl_429_4">4</a>] This underscores the special attention that infants with renal tumors require, with respect to timing and type of treatment and the importance of a dedicated expert pediatric oncology setting.</p><p id="CDR0000062789__842">Standard treatment options for stages I and II (80% of patients) and stage III (classic and mixed subtypes) congenital mesoblastic nephroma include the following:</p><ol id="CDR0000062789__897"><li class="half_rhythm"><div><a href="#CDR0000062789__1040">Nephrectomy only</a>.</div></li><li class="half_rhythm"><div><a href="#CDR0000062789__1041">Adjuvant chemotherapy</a> (stage III cellular subtype).</div></li></ol><div id="CDR0000062789__1040"><h4>Nephrectomy</h4><p id="CDR0000062789__844">Evidence (nephrectomy):</p><ol id="CDR0000062789__1944"><li class="half_rhythm"><div>In a SIOP/Gesellschaft für Pädiatrische Hämatologie und Onkologie (GPOH) nephroblastoma study, 111 patients with congenital mesoblastic nephromas demonstrated a 5-year RFS rate of 93.2% and a 5-year OS rate of 96.8%.[<a class="bk_pop" href="#CDR0000062789_rl_429_8">8</a>]<ul id="CDR0000062789__1945"><li class="half_rhythm"><div>Sixty-seven patients had classical congenital mesoblastic nephromas (60%), 29 patients had the cellular subtype (26%), and 15 patients had the mixed subtype (14%). The 5-year RFS rate was significantly superior for the classical type (98%) compared with the cellular type (89%, <i>P</i> = .039) or mixed type (80%, <i>P</i> = .002). There was no significant difference in OS by tumor types.</div></li><li class="half_rhythm"><div>Tumor stage consisted of stage I (35%), stage II (50%), and stage III (15%). </div></li><li class="half_rhythm"><div> Ninety-one patients were treated with surgery alone, and 19 patients were treated with chemotherapy in addition to surgery (12 preoperatively and 11 postoperatively).</div></li><li class="half_rhythm"><div>Seven patients relapsed (five local and two combined) and three patients died because of local relapse (one of each histologic type).</div></li><li class="half_rhythm"><div>Tissue was available for translocation analysis from 79 of the 111 tumors. Within the group of cellular congenital mesoblastic nephromas, patients who had translocation-positive tumors had a significantly improved RFS compared with the patients who had translocation-negative tumors (5-year RFS rate, 100% vs. 73%).</div></li></ul></div></li></ol></div><div id="CDR0000062789__1041"><h4>Adjuvant chemotherapy</h4><p id="CDR0000062789__1042">Adjuvant chemotherapy has been recommended for patients with stage III cellular subtype mesoblastic nephromas who are aged 3 months or older at diagnosis.[<a class="bk_pop" href="#CDR0000062789_rl_429_5">5</a>] In a study of stage III cellular type congenital mesoblastic nephroma, 7 of 12 patients who were treated with surgery only suffered from a relapse, while 4 of 14 patients who were treated with adjuvant chemotherapy (primarily dactinomycin/vincristine and sometimes doxorubicin) developed a relapse.[<a class="bk_pop" href="#CDR0000062789_rl_429_1">1</a>,<a class="bk_pop" href="#CDR0000062789_rl_429_5">5</a>,<a class="bk_pop" href="#CDR0000062789_rl_429_10">10</a>] Cyclophosphamide and ifosfamide have been combined with these agents and have shown activity.[<a class="bk_pop" href="#CDR0000062789_rl_429_11">11</a>]</p><p id="CDR0000062789__1311">Infants younger than 2 months with incompletely resected, stage III disease may not need chemotherapy.[<a class="bk_pop" href="#CDR0000062789_rl_429_1">1</a>]</p><p id="CDR0000062789__1871">(Refer to the <a href="#CDR0000062789__1312">Treatment of Recurrent Congenital Mesoblastic Nephroma</a> section of this summary for information about recurrent disease.)</p></div></div><div id="CDR0000062789__1951"><h3>Treatment options under clinical evaluation for congenital mesoblastic nephroma</h3><p id="CDR0000062789__1955">Information about National Cancer Institute (NCI)–supported clinical trials can be found on the <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NCI website</a>. For information about clinical trials sponsored by other organizations, refer to the <a href="https://clinicaltrials.gov/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">ClinicalTrials.gov website</a>.</p><p id="CDR0000062789__1953">The following is an example of a national and/or institutional clinical trial that is currently being conducted:</p><ul id="CDR0000062789__1954"><li class="half_rhythm"><div>
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<b><a href="https://www.cancer.gov/clinicaltrials/NCT03834961" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">ADVL1823 (NCT03834961)</a></b> (Larotrectinib in Treating Patients With Previously Untreated TRK Fusion Solid Tumors and TRK Fusion Relapsed Acute Leukemia)<b>:</b> This is a phase II trial to study how well larotrectinib works in treating patients with previously untreated TRK fusion solid tumors and TRK fusion acute leukemia that has come back. Larotrectinib is a highly selective oral small molecule inhibitor of the TRK family of tyrosine kinases (TRKA, TRKB, and TRKC), which are encoded by the <i>NTRK</i> genes. Larotrectinib will be administered twice daily on a continuous dosing schedule.</div></li></ul></div><div id="CDR0000062789__TrialSearch_429_sid_6"><h3>Current Clinical Trials</h3><p id="CDR0000062789__TrialSearch_429_22">Use our <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/advanced-search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">advanced clinical trial search</a> to find NCI-supported cancer clinical trials that are now enrolling patients. The search can be narrowed by location of the trial, type of treatment, name of the drug, and other criteria. <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">General information</a> about clinical trials is also available.</p></div><div id="CDR0000062789_rl_429"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_429_1">England RJ, Haider N, Vujanic GM, et al.: Mesoblastic nephroma: a report of the United Kingdom Children's Cancer and Leukaemia Group (CCLG). Pediatr Blood Cancer 56 (5): 744-8, 2011.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_429_2">Jehangir S, Kurian JJ, Selvarajah D, et al.: Recurrent and metastatic congenital mesoblastic nephroma: where does the evidence stand? Pediatr Surg Int 33 (11): 1183-1188, 2017.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_429_3">van den Heuvel-Eibrink MM, Grundy P, Graf N, et al.: Characteristics and survival of 750 children diagnosed with a renal tumor in the first seven months of life: A collaborative study by the SIOP/GPOH/SFOP, NWTSG, and UKCCSG Wilms tumor study groups. Pediatr Blood Cancer 50 (6): 1130-4, 2008.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_429_4">Gooskens SL, Houwing ME, Vujanic GM, et al.: Congenital mesoblastic nephroma 50 years after its recognition: A narrative review. Pediatr Blood Cancer 64 (7): , 2017.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_429_5">Furtwaengler R, Reinhard H, Leuschner I, et al.: Mesoblastic nephroma--a report from the Gesellschaft fur Pädiatrische Onkologie und Hämatologie (GPOH). Cancer 106 (10): 2275-83, 2006.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_429_6">El Demellawy D, Cundiff CA, Nasr A, et al.: Congenital mesoblastic nephroma: a study of 19 cases using immunohistochemistry and ETV6-NTRK3 fusion gene rearrangement. Pathology 48 (1): 47-50, 2016.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_429_7">Argani P, Ladanyi M: Recent advances in pediatric renal neoplasia. Adv Anat Pathol 10 (5): 243-60, 2003.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_429_8">Vokuhl C, Nourkami-Tutdibi N, Furtwängler R, et al.: ETV6-NTRK3 in congenital mesoblastic nephroma: A report of the SIOP/GPOH nephroblastoma study. Pediatr Blood Cancer 65 (4): , 2018.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_429_9">Knezevich SR, Garnett MJ, Pysher TJ, et al.: ETV6-NTRK3 gene fusions and trisomy 11 establish a histogenetic link between mesoblastic nephroma and congenital fibrosarcoma. Cancer Res 58 (22): 5046-8, 1998.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_429_10">Bayindir P, Guillerman RP, Hicks MJ, et al.: Cellular mesoblastic nephroma (infantile renal fibrosarcoma): institutional review of the clinical, diagnostic imaging, and pathologic features of a distinctive neoplasm of infancy. Pediatr Radiol 39 (10): 1066-74, 2009.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_429_11">McCahon E, Sorensen PH, Davis JH, et al.: Non-resectable congenital tumors with the ETV6-NTRK3 gene fusion are highly responsive to chemotherapy. Med Pediatr Oncol 40 (5): 288-92, 2003.</div></li></ol></div></div><div id="CDR0000062789__20"><h2 id="_CDR0000062789__20_">Ewing Sarcoma of the Kidney </h2><div id="CDR0000062789__889"><h3>General Information About Ewing Sarcoma of the Kidney</h3><p id="CDR0000062789__21">Ewing sarcoma (previously known as neuroepithelial tumor) of the kidney is extremely rare and demonstrates a unique proclivity for young adults. It is a highly aggressive neoplasm, more often presenting with large tumors and penetration of the renal capsule, extension into the renal vein, and in 40% of cases, evidence of metastases.[<a class="bk_pop" href="#CDR0000062789_rl_20_1">1</a>-<a class="bk_pop" href="#CDR0000062789_rl_20_3">3</a>] </p><p id="CDR0000062789__1043">Ewing sarcoma of the kidney is characterized by CD99 (MIC-2) positivity and
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the detection of EWS/FLI-1 fusion transcripts. Focal, atypical histologic features
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have been seen, including clear cell sarcoma, rhabdoid tumor, malignant
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peripheral nerve sheath tumors, and paraganglioma.[<a class="bk_pop" href="#CDR0000062789_rl_20_1">1</a>,<a class="bk_pop" href="#CDR0000062789_rl_20_4">4</a>] </p></div><div id="CDR0000062789__106"><h3>Treatment of Ewing Sarcoma of the Kidney</h3><p id="CDR0000062789__849">There is no standard treatment option for Ewing sarcoma of the kidney. However, treatment with chemotherapy and radiation therapy and an aggressive surgical approach seem to be associated with a better outcome than previously reported.[<a class="bk_pop" href="#CDR0000062789_rl_20_2">2</a>] Consideration should also be given to substituting cyclophosphamide for ifosfamide in patients after they have undergone a nephrectomy. [<a class="bk_pop" href="#CDR0000062789_rl_20_2">2</a>,<a class="bk_pop" href="#CDR0000062789_rl_20_3">3</a>] </p><p id="CDR0000062789__1044">Treatment
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according to Ewing sarcoma protocols should be considered.[<a class="bk_pop" href="#CDR0000062789_rl_20_1">1</a>]</p><p id="CDR0000062789__2012">(Refer to the PDQ summary on <a href="/books/n/pdqcis/CDR0000062841/">Ewing Sarcoma Treatment</a> for more information.) </p></div><div id="CDR0000062789__TrialSearch_20_sid_7"><h3>Current Clinical Trials</h3><p id="CDR0000062789__TrialSearch_20_22">Use our <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/advanced-search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">advanced clinical trial search</a> to find NCI-supported cancer clinical trials that are now enrolling patients. The search can be narrowed by location of the trial, type of treatment, name of the drug, and other criteria. <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">General information</a> about clinical trials is also available.</p></div><div id="CDR0000062789_rl_20"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_20_1">Parham DM, Roloson GJ, Feely M, et al.: Primary malignant neuroepithelial tumors of the kidney: a clinicopathologic analysis of 146 adult and pediatric cases from the National Wilms' Tumor Study Group Pathology Center. Am J Surg Pathol 25 (2): 133-46, 2001.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_20_2">Tagarelli A, Spreafico F, Ferrari A, et al.: Primary renal soft tissue sarcoma in children. Urology 80 (3): 698-702, 2012.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_20_3">Rowe RG, Thomas DG, Schuetze SM, et al.: Ewing sarcoma of the kidney: case series and literature review of an often overlooked entity in the diagnosis of primary renal tumors. Urology 81 (2): 347-53, 2013.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_20_4">Ellison DA, Parham DM, Bridge J, et al.: Immunohistochemistry of primary malignant neuroepithelial tumors of the kidney: a potential source of confusion? A study of 30 cases from the National Wilms Tumor Study Pathology Center. Hum Pathol 38 (2): 205-11, 2007.</div></li></ol></div></div><div id="CDR0000062789__1241"><h2 id="_CDR0000062789__1241_">Primary Renal Myoepithelial Carcinoma</h2><div id="CDR0000062789__1292"><h3>General Information About Primary Renal Myoepithelial Carcinoma</h3><p id="CDR0000062789__1242">Myoepithelial carcinomas are aggressive malignancies primarily affecting soft tissues with occasional visceral origin. Approximately 20% of all reported cases have been described in children and are associated with a particularly unfavorable outcome, frequent development of metastases, and short overall survival.[<a class="bk_pop" href="#CDR0000062789_rl_1241_1">1</a>] </p><p id="CDR0000062789__1253">Two cases of primary renal myoepithelial carcinoma have occurred in children, and both cases had a translocation involving <i>EWSR1</i> and the novel fusion partner <i>KLF15</i>, a transcription factor uniquely functioning within the kidney. Helpful features to establish the diagnosis include coexpression of cytokeratins, S-100, and smooth muscle markers, and the documentation of <i>EWSR1</i> rearrangements.[<a class="bk_pop" href="#CDR0000062789_rl_1241_2">2</a>]</p></div><div id="CDR0000062789__1293"><h3>Treatment of Primary Renal Myoepithelial Carcinoma</h3><p id="CDR0000062789__1249">Although no standard therapy has been established, surgical resection of the primary tumor and pulmonary nodules (if present) has been used in addition to chemotherapy and radiation therapy.[<a class="bk_pop" href="#CDR0000062789_rl_1241_2">2</a>]</p></div><div id="CDR0000062789_rl_1241"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_1241_1">Gleason BC, Fletcher CD: Myoepithelial carcinoma of soft tissue in children: an aggressive neoplasm analyzed in a series of 29 cases. Am J Surg Pathol 31 (12): 1813-24, 2007. [<a href="https://pubmed.ncbi.nlm.nih.gov/18043035" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 18043035</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1241_2">Cajaiba MM, Jennings LJ, Rohan SM, et al.: Expanding the Spectrum of Renal Tumors in Children: Primary Renal Myoepithelial Carcinomas With a Novel EWSR1-KLF15 Fusion. Am J Surg Pathol 40 (3): 386-94, 2016. [<a href="https://pubmed.ncbi.nlm.nih.gov/26523541" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 26523541</span></a>]</div></li></ol></div></div><div id="CDR0000062789__150"><h2 id="_CDR0000062789__150_">Cystic Partially Differentiated Nephroblastoma </h2><div id="CDR0000062789__891"><h3>General Information About Cystic Partially Differentiated Nephroblastoma</h3><p id="CDR0000062789__151">Cystic partially differentiated nephroblastoma is a rare cystic variant of Wilms tumor (1%), with unique pathologic and clinical characteristics. It is composed entirely of cysts, and their thin septa are the only solid portion of the tumor. The septa contain blastemal cells in any amount with or without embryonal stromal or epithelial cell type. Several pathologic features distinguish this neoplasm from standard Wilms tumor. <i>DICER1</i> mutations have not been reported in cystic partially differentiated nephroblastoma, which supports a distinction between multilocular cystic nephromas and cystic partially differentiated nephroblastoma.[<a class="bk_pop" href="#CDR0000062789_rl_150_1">1</a>]</p><p id="CDR0000062789__969">Recurrence has been reported after tumor spillage during surgery.[<a class="bk_pop" href="#CDR0000062789_rl_150_2">2</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335150/" class="def">Level of evidence: 3iiiA</a>]</p><p id="CDR0000062789__964">(Refer to the <a href="#CDR0000062789__898">Clinical Features of Wilms Tumor</a> and <a href="#CDR0000062789__900">Diagnostic and Staging Evaluation for Wilms Tumor</a> sections of this summary for more information about the clinical features and diagnostic evaluation of childhood kidney tumors.)</p></div><div id="CDR0000062789__855"><h3>Treatment of Cystic Partially Differentiated Nephroblastoma</h3><p id="CDR0000062789__856">Standard treatment options for cystic partially differentiated nephroblastoma include the following:</p><ol id="CDR0000062789__857"><li class="half_rhythm"><div>Surgery. Patients with stage I disease have a 100% survival rate with surgery alone.[<a class="bk_pop" href="#CDR0000062789_rl_150_3">3</a>] </div></li><li class="half_rhythm"><div>Surgery and adjuvant chemotherapy. Patients with stage II disease have an excellent outcome with tumor resection followed by postoperative vincristine and dactinomycin.[<a class="bk_pop" href="#CDR0000062789_rl_150_3">3</a>]</div></li></ol></div><div id="CDR0000062789_rl_150"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_150_1">Cajaiba MM, Khanna G, Smith EA, et al.: Pediatric cystic nephromas: distinctive features and frequent DICER1 mutations. Hum Pathol 48: 81-7, 2016. [<a href="/pmc/articles/PMC4979561/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC4979561</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/26772403" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 26772403</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_150_2">Baker JM, Viero S, Kim PC, et al.: Stage III cystic partially differentiated nephroblastoma recurring after nephrectomy and chemotherapy. Pediatr Blood Cancer 50 (1): 129-31, 2008. [<a href="https://pubmed.ncbi.nlm.nih.gov/16786584" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 16786584</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_150_3">Blakely ML, Shamberger RC, Norkool P, et al.: Outcome of children with cystic partially differentiated nephroblastoma treated with or without chemotherapy. J Pediatr Surg 38 (6): 897-900, 2003. [<a href="https://pubmed.ncbi.nlm.nih.gov/12778388" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 12778388</span></a>]</div></li></ol></div></div><div id="CDR0000062789__383"><h2 id="_CDR0000062789__383_">Multilocular Cystic Nephroma</h2><div id="CDR0000062789__892"><h3>General Information About Multilocular Cystic Nephroma</h3><p id="CDR0000062789__1243">Multilocular cystic nephromas are uncommon benign lesions consisting of cysts lined by renal epithelium. They are characterized by a bimodal age distribution, affecting either infants/young children or adult females. These lesions can occur bilaterally, and a familial pattern has been reported.</p><p id="CDR0000062789__1244">Multilocular cystic nephroma has been associated with pleuropulmonary blastoma and the <i>DICER1</i> mutation. Anaplastic sarcoma of the kidney has also been associated with the <i>DICER1</i> mutation.[<a class="bk_pop" href="#CDR0000062789_rl_383_1">1</a>] This is in contrast to adult cystic nephromas, which lack <i>DICER1</i> mutations, and supports the difference between adult and pediatric cases. Genetic counseling, <i>DICER1</i> mutation testing, and screening for lung lesions of a solid or cystic nature should be considered.[<a class="bk_pop" href="#CDR0000062789_rl_383_2">2</a>-<a class="bk_pop" href="#CDR0000062789_rl_383_5">5</a>]</p><p id="CDR0000062789__1245">(Refer to the <a href="#CDR0000062789__898">Clinical Features of Wilms Tumor</a> and <a href="#CDR0000062789__900">Diagnostic and Staging Evaluation for Wilms Tumor</a> sections of this summary for more information about the clinical features and diagnostic evaluation of childhood kidney tumors.)</p></div><div id="CDR0000062789__858"><h3>Treatment of Multilocular Cystic Nephroma</h3><p id="CDR0000062789__859">The standard treatment option for multilocular cystic nephroma is surgery.</p></div><div id="CDR0000062789_rl_383"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_383_1">Wu MK, Goudie C, Druker H, et al.: Evolution of Renal Cysts to Anaplastic Sarcoma of Kidney in a Child With DICER1 Syndrome. Pediatr Blood Cancer 63 (7): 1272-5, 2016.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_383_2">Dehner LP, Messinger YH, Schultz KA, et al.: Pleuropulmonary Blastoma: Evolution of an Entity as an Entry into a Familial Tumor Predisposition Syndrome. Pediatr Dev Pathol 18 (6): 504-11, 2015 Nov-Dec.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_383_3">Doros LA, Rossi CT, Yang J, et al.: DICER1 mutations in childhood cystic nephroma and its relationship to DICER1-renal sarcoma. Mod Pathol 27 (9): 1267-80, 2014.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_383_4">Cajaiba MM, Khanna G, Smith EA, et al.: Pediatric cystic nephromas: distinctive features and frequent DICER1 mutations. Hum Pathol 48: 81-7, 2016.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_383_5">Li Y, Pawel BR, Hill DA, et al.: Pediatric Cystic Nephroma Is Morphologically, Immunohistochemically, and Genetically Distinct From Adult Cystic Nephroma. Am J Surg Pathol 41 (4): 472-481, 2017.</div></li></ol></div></div><div id="CDR0000062789__438"><h2 id="_CDR0000062789__438_">Primary Renal Synovial Sarcoma</h2><div id="CDR0000062789__893"><h3>General Information About Primary Renal Synovial Sarcoma</h3><p id="CDR0000062789__439">Primary renal synovial sarcoma is a subset of embryonal sarcoma of the kidney that occurs more often in young adults. It is similar in histology to the monophasic spindle cell synovial sarcoma and contains cystic structures derived from dilated, trapped renal tubules. It is considered an aggressive tumor with adverse patient outcomes in more than 50% of cases (n = 16).[<a class="bk_pop" href="#CDR0000062789_rl_438_1">1</a>] Primary renal synovial sarcoma is characterized by the t(x;18)(p11;q11) <i><a href="/snp/?term=18" class="bk_tag" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=snp">SS18</a></i>-<i>SSX</i> translocation, and a second alternative gene fusion variant, <i><a href="/snp/?term=18" class="bk_tag" ref="pagearea=body&targetsite=entrez&targetcat=term&targettype=snp">SS18</a>-NEDD4</i>, has also been identified.</p><p id="CDR0000062789__965">(Refer to the <a href="#CDR0000062789__898">Clinical Features of Wilms Tumor</a> and <a href="#CDR0000062789__900">Diagnostic and Staging Evaluation for Wilms Tumor</a> sections of this summary for more information about the clinical features and diagnostic evaluation of childhood kidney tumors.)</p></div><div id="CDR0000062789__860"><h3>Treatment of Primary Renal Synovial Sarcoma</h3><p id="CDR0000062789__861">The standard treatment option for primary renal synovial sarcoma is chemotherapy. The chemotherapy regimens used differ from those traditionally used for Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_438_2">2</a>]</p></div><div id="CDR0000062789_rl_438"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_438_1">Schoolmeester JK, Cheville JC, Folpe AL: Synovial sarcoma of the kidney: a clinicopathologic, immunohistochemical, and molecular genetic study of 16 cases. Am J Surg Pathol 38 (1): 60-5, 2014.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_438_2">Argani P, Faria PA, Epstein JI, et al.: Primary renal synovial sarcoma: molecular and morphologic delineation of an entity previously included among embryonal sarcomas of the kidney. Am J Surg Pathol 24 (8): 1087-96, 2000.</div></li></ol></div></div><div id="CDR0000062789__440"><h2 id="_CDR0000062789__440_">Anaplastic Sarcoma of the Kidney</h2><div id="CDR0000062789__894"><h3>General Information About Anaplastic Sarcoma of the Kidney</h3><p id="CDR0000062789__441">Anaplastic sarcoma of the kidney is a rare renal tumor that has been identified mainly in patients younger than 15 years. </p><p id="CDR0000062789__1046">Patients present with a renal mass, with the most common sites of metastases being the lungs, liver, and bones. (Refer to the <a href="#CDR0000062789__898">Clinical Features of Wilms Tumor</a> and <a href="#CDR0000062789__900">Diagnostic and Staging Evaluation for Wilms Tumor</a> sections of this summary for more information about the clinical features and diagnostic evaluation of childhood kidney tumors.) </p><p id="CDR0000062789__1047">Cytogenetic abnormalities such as rearrangement between 10q21 and 18p11.2 have been reported.[<a class="bk_pop" href="#CDR0000062789_rl_440_1">1</a>] These tumors show pathologic features similar to those of pleuropulmonary blastoma of childhood (refer to the PDQ summary on <a href="/books/n/pdqcis/CDR0000799361/">Childhood Pleuropulmonary Blastoma Treatment</a> for more information) and undifferentiated embryonal sarcoma of the liver (refer to the <a href="/books/n/pdqcis/CDR0000062836/#CDR0000062836__378">Treatment Options for Undifferentiated Embryonal Sarcoma of the Liver</a> section in the PDQ summary on <a href="/books/n/pdqcis/CDR0000062836/">Childhood Liver Cancer Treatment</a> for more information). Because of the relationship between pleuropulmonary blastoma and renal sarcomas, genetic counseling and testing for a germline <i>DICER1</i> mutation should be considered. Screening for lung lesions of a solid or cystic nature should also be considered on the basis of age and <i>DICER1</i> mutation testing.[<a class="bk_pop" href="#CDR0000062789_rl_440_2">2</a>]</p></div><div id="CDR0000062789__862"><h3>Treatment of Anaplastic Sarcoma of the Kidney</h3><p id="CDR0000062789__863">There is no standard treatment option for anaplastic sarcoma of the kidney. In the past, these tumors have been identified as anaplastic Wilms tumor and treated accordingly.[<a class="bk_pop" href="#CDR0000062789_rl_440_3">3</a>]</p></div><div id="CDR0000062789_rl_440"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_440_1">Gomi K, Hamanoue S, Tanaka M, et al.: Anaplastic sarcoma of the kidney with chromosomal abnormality: first report on cytogenetic findings. Hum Pathol 41 (10): 1495-9, 2010.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_440_2">Doros LA, Rossi CT, Yang J, et al.: DICER1 mutations in childhood cystic nephroma and its relationship to DICER1-renal sarcoma. Mod Pathol 27 (9): 1267-80, 2014.</div></li><li><div class="bk_ref" id="CDR0000062789_rl_440_3">Vujanić GM, Kelsey A, Perlman EJ, et al.: Anaplastic sarcoma of the kidney: a clinicopathologic study of 20 cases of a new entity with polyphenotypic features. Am J Surg Pathol 31 (10): 1459-68, 2007.</div></li></ol></div></div><div id="CDR0000062789__436"><h2 id="_CDR0000062789__436_">Nephroblastomatosis </h2><div id="CDR0000062789__890"><h3>General Information About Nephroblastomatosis (Diffuse Hyperplastic Perilobar Nephroblastomatosis)</h3><p id="CDR0000062789__437">Some multifocal nephrogenic rests may become hyperplastic, which may produce a thick rind of blastemal or tubular cells that enlarge the kidney. Radiological studies may be helpful in making the difficult distinction between diffuse hyperplastic perilobar nephroblastomatosis and Wilms tumor. On magnetic resonance imaging, nephrogenic rests appear homogeneous and hypointense with contrast, whereas Wilms tumor has mixed echogenicity and inhomogeneous appearance. Incisional biopsies are difficult to interpret, and it is essential that the biopsy includes the juncture between the lesion and surrounding renal parenchyma.[<a class="bk_pop" href="#CDR0000062789_rl_436_1">1</a>] Differentiation may occur after chemotherapy is administered. </p></div><div id="CDR0000062789__850"><h3>Treatment of Nephroblastomatosis (Diffuse Hyperplastic Perilobar Nephroblastomatosis)</h3><p id="CDR0000062789__851">Treatment options for diffuse hyperplastic perilobar nephroblastomatosis include the following:</p><ol id="CDR0000062789__852"><li class="half_rhythm"><div>Preoperative chemotherapy.</div></li><li class="half_rhythm"><div>Renal-sparing surgery. Given the high incidence of bilaterality and subsequent Wilms tumors, renal-sparing surgery may be indicated.[<a class="bk_pop" href="#CDR0000062789_rl_436_1">1</a>]</div></li></ol><p id="CDR0000062789__1302">Evidence (preoperative chemotherapy and surgery):</p><ol id="CDR0000062789__1303"><li class="half_rhythm"><div class="half_rhythm">In a series of 52 patients with diffuse hyperplastic perilobar nephroblastomatosis, 33 patients were treated with chemotherapy and/or radiation therapy initially, 16 patients underwent unilateral nephrectomy followed by adjuvant therapy, and 3 patients were observed only.[<a class="bk_pop" href="#CDR0000062789_rl_436_1">1</a>]<ul id="CDR0000062789__1304"><li class="half_rhythm"><div>A total of 24 patients developed Wilms tumor (including the 3 patients who were observed only), at a median of 30 months.</div></li><li class="half_rhythm"><div>Eighteen of the 33 patients who received chemotherapy alone developed a Wilms tumor.</div></li><li class="half_rhythm"><div>Of 16 patients who underwent a nephrectomy and adjuvant therapy, 3 developed Wilms tumor, despite the fact that 14 of 16 patients had bilateral disease.</div></li><li class="half_rhythm"><div>Thirty-three percent of the patients who developed Wilms tumor had anaplastic Wilms tumor at some time during their course, probably as a result of selection of chemotherapy-resistant tumors; thus, early detection is critical.</div></li></ul></div><div class="half_rhythm">On the basis of this report, it is recommended that patients with diffuse hyperplastic perilobar nephroblastomatosis be monitored by imaging at a maximum interval of 3 months, for a minimum of 7 years; complete resection of growing lesions should be strongly considered because of the high incidence of anaplasia after chemotherapy.[<a class="bk_pop" href="#CDR0000062789_rl_436_1">1</a>]</div></li></ol></div><div id="CDR0000062789_rl_436"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_436_1">Perlman EJ, Faria P, Soares A, et al.: Hyperplastic perilobar nephroblastomatosis: long-term survival of 52 patients. Pediatr Blood Cancer 46 (2): 203-21, 2006.</div></li></ol></div></div><div id="CDR0000062789__108"><h2 id="_CDR0000062789__108_">Treatment of Recurrent Childhood Kidney Tumors</h2><p id="CDR0000062789__864">Patients with most forms of recurrent childhood cancer should be considered for treatment on
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available phase I and phase II clinical trials. Other treatment options for recurrent Wilms tumor, clear cell sarcoma of the kidney, and congenital mesoblastic nephroma are discussed below.</p><p id="CDR0000062789__1908">Regardless of whether a decision is made to pursue disease-directed therapy at the time of progression, palliative care remains a central focus of management. This ensures that quality of life is maximized while attempting to reduce symptoms and stress related to the terminal illness.</p><p id="CDR0000062789__1317"><a class="figpopup" href="/books/NBK65842.23/table/CDR0000062789__919/?report=objectonly" target="object" rid-figpopup="figCDR0000062789919" rid-ob="figobCDR0000062789919">Table 9</a> describes the treatment options for some forms of recurrent childhood kidney tumors.</p><div id="CDR0000062789__919" class="table"><h3><span class="title">Table 9. Treatment Options for Recurrent Childhood Kidney Tumors</span></h3><p class="large-table-link" style="display:none"><span class="right"><a href="/books/NBK65842.23/table/CDR0000062789__919/?report=objectonly" target="object">View in own window</a></span></p><div class="large_tbl" id="__CDR0000062789__919_lrgtbl__"><table class="no_top_margin"><thead><tr><th colspan="1" rowspan="1" style="vertical-align:top;">Tumor Type</th><th colspan="1" rowspan="1" style="vertical-align:top;">Treatment Options</th></tr></thead><tbody><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Standard-risk relapsed Wilms tumor</td><td colspan="1" rowspan="1" style="vertical-align:top;"><a href="#CDR0000062789__867">Surgery, radiation therapy, and chemotherapy</a></td></tr><tr><td colspan="1" rowspan="2" style="vertical-align:top;">High-risk and very high-risk relapsed Wilms tumor</td><td colspan="1" rowspan="1" style="vertical-align:top;"><a href="#CDR0000062789__872">Chemotherapy, surgery, and/or radiation therapy</a></td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;"><a href="#CDR0000062789__876">Hematopoietic stem cell transplantation</a></td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Recurrent clear cell sarcoma of the kidney</td><td colspan="1" rowspan="1" style="vertical-align:top;"><a href="#CDR0000062789__883">Chemotherapy, surgery, and/or radiation therapy </a></td></tr><tr><td colspan="1" rowspan="1" style="vertical-align:top;">Recurrent congenital mesoblastic nephroma</td><td colspan="1" rowspan="1" style="vertical-align:top;"><a href="#CDR0000062789__1313">Surgery, chemotherapy, and radiation therapy</a></td></tr></tbody></table></div></div><div id="CDR0000062789__1966"><h3>Treatment and Outcomes of Recurrent Wilms Tumor</h3><div id="CDR0000062789__895"><h4>Prognosis, prognostic factors, and risk categories for recurrent Wilms tumor</h4><p id="CDR0000062789__531">Approximately 15% of patients with favorable histology (FH) Wilms tumor and 50% of patients with anaplastic histology Wilms tumor experience recurrence.[<a class="bk_pop" href="#CDR0000062789_rl_108_1">1</a>] The most common site of relapse is lung, followed by abdomen/flank and liver. Recurrence in the brain (0.5%) or bone is rare in children with Wilms tumor.[<a class="bk_pop" href="#CDR0000062789_rl_108_2">2</a>,<a class="bk_pop" href="#CDR0000062789_rl_108_3">3</a>] Historically, the salvage rate for patients with recurrent FH Wilms tumor was 25% to 40%. As a result of modern treatment combinations, the outcome after recurrence has improved to up to 60%.[<a class="bk_pop" href="#CDR0000062789_rl_108_4">4</a>,<a class="bk_pop" href="#CDR0000062789_rl_108_5">5</a>] </p><p id="CDR0000062789__1049">A number of potential prognostic features influencing postrecurrence outcomes have been analyzed, but it is difficult to determine whether these factors are independent of each other. Also, the following prognostic factors appear to be changing as therapy for primary and recurrent Wilms tumor evolves:</p><ul id="CDR0000062789__532"><li class="half_rhythm"><div>Anaplastic histology.[<a class="bk_pop" href="#CDR0000062789_rl_108_6">6</a>]</div></li><li class="half_rhythm"><div>Advanced tumor stage.[<a class="bk_pop" href="#CDR0000062789_rl_108_6">6</a>]</div></li><li class="half_rhythm"><div>Sex. Sex was predictive of outcome, with males faring worse than females.[<a class="bk_pop" href="#CDR0000062789_rl_108_4">4</a>,<a class="bk_pop" href="#CDR0000062789_rl_108_7">7</a>]</div></li></ul><p id="CDR0000062789__533">The National Wilms Tumor Study (NWTS)-5 trial (<a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5 [COG-Q9401/NCT00002611]</a>) showed that time to recurrence and site of recurrence are no longer prognostically significant.[<a class="bk_pop" href="#CDR0000062789_rl_108_4">4</a>,<a class="bk_pop" href="#CDR0000062789_rl_108_7">7</a>] However, in an International Society of Pediatric Oncology (SIOP) study, patients who experienced a pulmonary relapse within 12 months of diagnosis had a poorer prognosis (5-year overall survival [OS] rate, 47%) than did patients who experienced a pulmonary relapse 12 months or more after diagnosis (5-year OS rate, 75%).[<a class="bk_pop" href="#CDR0000062789_rl_108_8">8</a>]</p><p id="CDR0000062789__534">On the basis of these results, the following three risk categories have been identified:</p><ul id="CDR0000062789__535"><li class="half_rhythm"><div><b>Standard risk:</b> Patients with FH Wilms tumor who relapse after therapy with only vincristine and/or dactinomycin. These patients account for approximately 30% of recurrences and are expected to have event-free survival (EFS) rates of 70% to 80%.[<a class="bk_pop" href="#CDR0000062789_rl_108_5">5</a>] </div></li><li class="half_rhythm"><div><b>High risk:</b> Patients with FH Wilms tumor who relapse after therapy with three or more agents. These patients account for 45% to 50% of children with Wilms tumor who relapse and have survival rates in the 40% to 50% range.[<a class="bk_pop" href="#CDR0000062789_rl_108_5">5</a>]</div></li><li class="half_rhythm"><div><b>Very high risk:</b> Patients with recurrent anaplastic or blastemal-predominant Wilms tumor. These patients account for 10% to 15% of all Wilms tumor relapses and are expected to have survival rates in the 10% range.[<a class="bk_pop" href="#CDR0000062789_rl_108_5">5</a>,<a class="bk_pop" href="#CDR0000062789_rl_108_9">9</a>]</div></li></ul></div><div id="CDR0000062789__593"><h4>Treatment of standard-risk relapsed Wilms tumor</h4><p id="CDR0000062789__594">In children who had small stage I Wilms tumor and were treated with surgery alone, the EFS rate was 84%. All but one child who relapsed was salvaged with treatment tailored to the site of recurrence.[<a class="bk_pop" href="#CDR0000062789_rl_108_7">7</a>,<a class="bk_pop" href="#CDR0000062789_rl_108_10">10</a>]</p><p id="CDR0000062789__927">Successful retreatment can be accomplished for Wilms tumor patients whose initial therapy consisted of immediate nephrectomy followed by chemotherapy with vincristine and dactinomycin and who relapse.</p><p id="CDR0000062789__865">Treatment options for standard-risk relapsed Wilms tumor include the following:</p><ol id="CDR0000062789__866"><li class="half_rhythm"><div><a href="#CDR0000062789__1064">Surgery, radiation therapy, and chemotherapy</a>.</div></li></ol><div id="CDR0000062789__1064"><h5>Surgery, radiation therapy, and chemotherapy</h5><p id="CDR0000062789__867">Evidence (surgery, radiation therapy, and chemotherapy):</p><ol id="CDR0000062789__868"><li class="half_rhythm"><div>Fifty-eight patients were treated on the <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5</a> relapse protocol with surgical excision when feasible, radiation therapy, and courses of vincristine, doxorubicin, and cyclophosphamide alternating with etoposide and cyclophosphamide.[<a class="bk_pop" href="#CDR0000062789_rl_108_7">7</a>] <ul id="CDR0000062789__869"><li class="half_rhythm"><div>The 4-year EFS rate after relapse was 71%, and the OS rate was 82%. </div></li><li class="half_rhythm"><div>For patients whose site of relapse was only the lungs, the 4-year EFS rate was 68%, and the OS rate was 81%.</div></li></ul></div></li></ol></div></div><div id="CDR0000062789__595"><h4>Treatment of high-risk and very high-risk relapsed Wilms tumor</h4><p id="CDR0000062789__870">Treatment options for high-risk and very high-risk relapsed Wilms tumor include the following:</p><ol id="CDR0000062789__871"><li class="half_rhythm"><div><a href="#CDR0000062789__872">Chemotherapy, surgery, and/or radiation therapy</a>.</div></li><li class="half_rhythm"><div><a href="#CDR0000062789__876">Hematopoietic stem cell transplantation (HSCT)</a>.</div></li></ol><div id="CDR0000062789__872"><h5>Chemotherapy, surgery, and/or radiation therapy</h5><p id="CDR0000062789__873">Evidence (chemotherapy, surgery, and/or radiation therapy):</p><ol id="CDR0000062789__874"><li class="half_rhythm"><div>Approximately 50% of unilateral Wilms tumor patients who relapse or progress after initial treatment with vincristine, dactinomycin, and doxorubicin and radiation therapy can be successfully re-treated. Sixty patients with unilateral Wilms tumor were treated on the <a href="https://www.cancer.gov/clinicaltrials/NCT00002611" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NWTS-5</a> relapse protocol with alternating courses of cyclophosphamide/etoposide and carboplatin/etoposide, surgery, and radiation therapy.[<a class="bk_pop" href="#CDR0000062789_rl_108_4">4</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335132/" class="def">Level of evidence: 2A</a>] <ul id="CDR0000062789__875"><li class="half_rhythm"><div> The 4-year EFS rate for patients with high-risk Wilms tumor was 42%, and the OS rate was 48%.</div></li><li class="half_rhythm"><div>High-risk patients who relapsed in the lungs only had a 4-year EFS rate of 49% and an OS rate of 53%.</div></li></ul></div></li></ol><p id="CDR0000062789__1050">Patients with stage II, stage III, and stage IV anaplastic tumors at diagnosis have a very poor prognosis upon recurrence.[<a class="bk_pop" href="#CDR0000062789_rl_108_9">9</a>] The
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combination of ifosfamide, etoposide, and carboplatin demonstrated activity
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in this group of patients, but significant hematologic toxic effects have been
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observed.[<a class="bk_pop" href="#CDR0000062789_rl_108_11">11</a>]</p></div><div id="CDR0000062789__876"><h5>HSCT</h5><p id="CDR0000062789__1051">High-dose chemotherapy followed by autologous HSCT has been utilized for recurrent high-risk patients.[<a class="bk_pop" href="#CDR0000062789_rl_108_12">12</a>,<a class="bk_pop" href="#CDR0000062789_rl_108_13">13</a>]; [<a class="bk_pop" href="#CDR0000062789_rl_108_14">14</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000641572/" class="def">Level of evidence: 3ii</a>]</p><p id="CDR0000062789__877">Evidence (HSCT):</p><ol id="CDR0000062789__878"><li class="half_rhythm"><div>The outcomes of 253 patients with relapsed Wilms tumor who received high-dose chemotherapy followed by autologous HSCT between 1990 and 2013 were reported to and reviewed by the Center for International Blood and Marrow Transplantation Research.[<a class="bk_pop" href="#CDR0000062789_rl_108_15">15</a>]<ul id="CDR0000062789__1899"><li class="half_rhythm"><div>The 5-year estimate for EFS was 36%, and the 5-year estimate for OS was 45%.</div></li><li class="half_rhythm"><div>Relapse of primary disease was the cause of death in 81% of the population.</div></li></ul></div></li><li class="half_rhythm"><div>In a single-institution series of 24 patients with relapsed and refractory Wilms tumor who were treated with high-dose chemotherapy followed by autologous stem cell rescue (HD-ASCR), the following results were reported:[<a class="bk_pop" href="#CDR0000062789_rl_108_14">14</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000641572/" class="def">Level of evidence: 3ii</a>] <ul id="CDR0000062789__1950"><li class="half_rhythm"><div>The 3-year disease-free survival (DFS) and OS rates were 46% and 60%, respectively; the 5-year DFS and OS rates were 40% and 54%, respectively. These rates are similar to those reported for conventional salvage therapies.</div></li><li class="half_rhythm"><div>No survival advantage was identified on the basis of time to relapse, disease state at time of HD-ASCR, initial stage, or site of relapse.</div></li><li class="half_rhythm"><div>No difference was found on the basis of age of diagnosis, sex, histology, or treatment with one versus two cycles of HD-ASCR.</div></li></ul></div></li></ol><p id="CDR0000062789__1052"> No randomized trials of chemotherapy versus transplant have been reported, and case series suffer from selection bias.</p><p id="CDR0000062789__880"> Patients in whom such salvage
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attempts fail should be offered treatment on available phase I or phase II
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studies.</p></div></div><div id="CDR0000062789__1824"><h4>Treatment options under clinical evaluation for recurrent Wilms tumor</h4><p id="CDR0000062789__1835">Information about National Cancer Institute (NCI)–supported clinical trials can be found on the <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NCI website</a>. For information about clinical trials sponsored by other organizations, refer to the <a href="https://clinicaltrials.gov/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">ClinicalTrials.gov website</a>.</p><p id="CDR0000062789__1825">The following is an example of a national and/or institutional clinical trial that is currently being conducted:</p><ul id="CDR0000062789__1826"><li class="half_rhythm"><div class="half_rhythm"><b><a href="https://www.cancer.gov/clinicaltrials/NCT03155620" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">APEC1621 (NCT03155620)</a></b> (Pediatric MATCH: Targeted Therapy Directed by Genetic Testing in Treating Pediatric Patients with Relapsed or Refractory Advanced Solid Tumors, Non-Hodgkin Lymphomas, or Histiocytic Disorders)<b>:</b> NCI-COG Pediatric Molecular Analysis for Therapeutic Choice (MATCH), referred to as Pediatric MATCH, will match targeted agents with specific molecular changes identified using a next-generation sequencing targeted assay of more than 4,000 different mutations across more than 160 genes in refractory and recurrent solid tumors. Children and adolescents aged 1 to 21 years are eligible for the trial.</div><div class="half_rhythm">Tumor tissue from progressive or recurrent disease must be available for molecular characterization. Patients with tumors that have molecular variants addressed by treatment arms included in the trial will be offered treatment on Pediatric MATCH. Additional information can be obtained on the <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/nci-supported/pediatric-match" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NCI website</a> and <a href="https://clinicaltrials.gov/ct2/show/NCT03155620" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">ClinicalTrials.gov website</a>.
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</div></li></ul></div></div><div id="CDR0000062789__598"><h3>Treatment of Recurrent Clear Cell Sarcoma of the Kidney</h3><p id="CDR0000062789__599">Clear cell sarcoma of the kidney has been characterized by late relapses. However, in trials after 1992, most relapses occurred within 3 years, and the most common sites of recurrence were the brain and the lungs.[<a class="bk_pop" href="#CDR0000062789_rl_108_16">16</a>,<a class="bk_pop" href="#CDR0000062789_rl_108_17">17</a>] In a series of 37 patients with clear cell sarcoma of the kidney who relapsed, the 5-year EFS rate after relapse was 18%, and the OS rate after relapse was 26%.[<a class="bk_pop" href="#CDR0000062789_rl_108_17">17</a>] </p><p id="CDR0000062789__1053">The optimal treatment of relapsed clear cell sarcoma of the kidney has not been established. Treatment of patients with recurrent clear cell sarcoma of the kidney depends on initial therapy and site of recurrence. </p><p id="CDR0000062789__881">Treatment options for recurrent clear cell sarcoma of the kidney include the following:</p><ol id="CDR0000062789__882"><li class="half_rhythm"><div>Chemotherapy, complete surgical resection (if possible), and/or radiation therapy.</div></li></ol><p id="CDR0000062789__883">Cyclophosphamide and carboplatin should be considered if not used initially. Patients with recurrent clear cell sarcoma of the kidney, in some cases involving the brain, have responded to treatment with ifosfamide, carboplatin, and etoposide (ICE) coupled with local control consisting of surgical resection, radiation therapy, or both.[<a class="bk_pop" href="#CDR0000062789_rl_108_17">17</a>]; [<a class="bk_pop" href="#CDR0000062789_rl_108_18">18</a>][<a href="/books/n/pdqcis/glossary_loe/def-item/glossary_loe_CDR0000335132/" class="def">Level of evidence: 2A</a>] </p><p id="CDR0000062789__954">The use of high-dose chemotherapy followed by HSCT is undefined in patients with recurrent clear cell sarcoma of the kidney. A total of 24 patients with relapsed clear cell sarcoma of the kidney received high-dose chemotherapy followed by autologous HSCT. Of those patients, 12 (50%) were alive without disease after a median of 52 months. Patients who had already achieved a second complete remission were more likely to receive high-dose chemotherapy.[<a class="bk_pop" href="#CDR0000062789_rl_108_13">13</a>,<a class="bk_pop" href="#CDR0000062789_rl_108_17">17</a>,<a class="bk_pop" href="#CDR0000062789_rl_108_18">18</a>]</p><div id="CDR0000062789__1817"><h4>Treatment options under clinical evaluation for recurrent clear cell sarcoma of the kidney</h4><p id="CDR0000062789__1836">Information about NCI-supported clinical trials can be found on the <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NCI website</a>. For information about clinical trials sponsored by other organizations, refer to the <a href="https://clinicaltrials.gov/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">ClinicalTrials.gov website</a>.</p><p id="CDR0000062789__1818">The following is an example of a national and/or institutional clinical trial that is currently being conducted:</p><ul id="CDR0000062789__1819"><li class="half_rhythm"><div class="half_rhythm"><b><a href="https://www.cancer.gov/clinicaltrials/NCT03155620" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">APEC1621 (NCT03155620)</a></b> (Pediatric MATCH: Targeted Therapy Directed by Genetic Testing in Treating Pediatric Patients with Relapsed or Refractory Advanced Solid Tumors, Non-Hodgkin Lymphomas, or Histiocytic Disorders)<b>:</b> NCI-COG Pediatric Molecular Analysis for Therapeutic Choice (MATCH), referred to as Pediatric MATCH, will match targeted agents with specific molecular changes identified using a next-generation sequencing targeted assay of more than 4,000 different mutations across more than 160 genes in refractory and recurrent solid tumors. Children and adolescents aged 1 to 21 years are eligible for the trial.</div><div class="half_rhythm">Tumor tissue from progressive or recurrent disease must be available for molecular characterization. Patients with tumors that have molecular variants addressed by treatment arms included in the trial will be offered treatment on Pediatric MATCH. Additional information can be obtained on the <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/nci-supported/pediatric-match" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NCI website</a> and <a href="https://clinicaltrials.gov/ct2/show/NCT03155620" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">ClinicalTrials.gov website</a>.
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</div></li></ul></div></div><div id="CDR0000062789__1312"><h3>Treatment of Recurrent Congenital Mesoblastic Nephroma</h3><p id="CDR0000062789__1313">Relapses were reported in 4% of patients with congenital mesoblastic nephroma, and all relapses occurred within 12 months after diagnosis. Most relapses occurred locally, although metastatic relapses have been reported.[<a class="bk_pop" href="#CDR0000062789_rl_108_19">19</a>] About 70% of patients who relapsed survived with individualized treatment comprising combinations of surgery, chemotherapy, and radiation therapy.[<a class="bk_pop" href="#CDR0000062789_rl_108_19">19</a>]</p><p id="CDR0000062789__1946">Targeted therapy should be considered for patients with recurrent or refractory disease containing the <i>ETV6-NTRK3</i> fusion. Larotrectinib and entrectinib are NTRK inhibitors that are approved for adult and pediatric patients with solid tumors that have an <i>NTRK</i> gene fusion without a known acquired resistance mutation, who are either metastatic or when surgical resection is likely to result in severe morbidity, and who have no satisfactory alternative treatments or whose cancer has progressed after treatment.[<a class="bk_pop" href="#CDR0000062789_rl_108_20">20</a>,<a class="bk_pop" href="#CDR0000062789_rl_108_21">21</a>]</p><div id="CDR0000062789__1314"><h4>Treatment options under clinical evaluation for recurrent congenital mesoblastic nephroma</h4><p id="CDR0000062789__1837">Information about NCI-supported clinical trials can be found on the <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NCI website</a>. For information about clinical trials sponsored by other organizations, refer to the <a href="https://clinicaltrials.gov/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">ClinicalTrials.gov website</a>.</p><p id="CDR0000062789__1838">The following are examples of national and/or institutional clinical trials that are currently being conducted:</p><ul id="CDR0000062789__1316"><li class="half_rhythm"><div class="half_rhythm"><b><a href="https://www.cancer.gov/clinicaltrials/NCT03155620" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">APEC1621 (NCT03155620)</a></b> (Pediatric MATCH: Targeted Therapy Directed by Genetic Testing in Treating Pediatric Patients with Relapsed or Refractory Advanced Solid Tumors, Non-Hodgkin Lymphomas, or Histiocytic Disorders)<b>:</b> NCI-COG Pediatric Molecular Analysis for Therapeutic Choice (MATCH), referred to as Pediatric MATCH, will match targeted agents with specific molecular changes identified using a next-generation sequencing targeted assay of more than 4,000 different mutations across more than 160 genes in refractory and recurrent solid tumors. Children and adolescents aged 1 to 21 years are eligible for the trial.</div><div class="half_rhythm">Tumor tissue from progressive or recurrent disease must be available for molecular characterization. Patients with tumors that have molecular variants addressed by treatment arms included in the trial will be offered treatment on Pediatric MATCH. Additional information can be obtained on the <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/nci-supported/pediatric-match" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NCI website</a> and <a href="https://clinicaltrials.gov/ct2/show/NCT03155620" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">ClinicalTrials.gov website</a>.</div><div class="half_rhythm">The cellular subtype of congenital mesoblastic nephroma, which commonly harbors the <i>ETV6-NTRK3</i> fusion, is associated with relapsed disease. Patients should consider enrolling on this trial because one of the treatment arms (<a href="https://www.cancer.gov/clinicaltrials/NCT03213704" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">APEC1621A [NCT03213704]</a>) uses larotrectinib, which inhibits <i>NTRK</i> fusions.
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</div></li><li class="half_rhythm"><div class="half_rhythm"><b><a href="https://www.cancer.gov/clinicaltrials/NCT02637687" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">LOXO-TRK-15003 (NCT02637687)</a></b> (Oral TRK Inhibitor LOXO-101 for Treatment of Advanced Pediatric Solid or Primary Central Nervous System [CNS] Tumors)<b>:</b> This is a multicenter, open-label, phase I study of pediatric patients with advanced solid
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or primary CNS tumors. LOXO-101 will be administered orally twice daily, with the
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dose adjusted by body surface area.</div></li><li class="half_rhythm"><div class="half_rhythm"><b><a href="https://www.cancer.gov/clinicaltrials/NCT02650401" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">RXDX-101-03 (NCT02650401)</a></b> (Study of RXDX-101 in Children With Recurrent or Refractory Solid Tumors and Primary CNS Tumors)<b>:</b> This is a four-part, open-label, phase I/Ib, dose-escalation study in pediatric patients with
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relapsed or refractory solid tumors, primary CNS tumors, neuroblastoma, and non-neuroblastoma, extracranial solid tumors with <i>NTRK1/2/3</i>, <i>ROS1</i>, or <i>ALK</i> gene
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rearrangements. The study is designed to explore the safety, maximum tolerated dose or
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recommended phase II dose, pharmacokinetics, and antitumor activity of entrectinib (RXDX-101).
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</div></li></ul></div></div><div id="CDR0000062789__TrialSearch_108_sid_14"><h3>Current Clinical Trials</h3><p id="CDR0000062789__TrialSearch_108_22">Use our <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/advanced-search" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">advanced clinical trial search</a> to find NCI-supported cancer clinical trials that are now enrolling patients. The search can be narrowed by location of the trial, type of treatment, name of the drug, and other criteria. <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">General information</a> about clinical trials is also available.</p></div><div id="CDR0000062789_rl_108"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_108_1">Green DM, Breslow NE, Beckwith JB, et al.: Effect of duration of treatment on treatment outcome and cost of treatment for Wilms' tumor: a report from the National Wilms' Tumor Study Group. J Clin Oncol 16 (12): 3744-51, 1998. [<a href="https://pubmed.ncbi.nlm.nih.gov/9850017" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 9850017</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_2">Venkatramani R, Chi YY, Coppes MJ, et al.: Outcome of patients with intracranial relapse enrolled on national Wilms Tumor Study Group clinical trials. Pediatr Blood Cancer 64 (7): , 2017. [<a href="/pmc/articles/PMC5477465/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC5477465</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/28097788" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 28097788</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_3">Iaboni DSM, Chi YY, Kim Y, et al.: Outcome of Wilms tumor patients with bone metastasis enrolled on National Wilms Tumor Studies 1-5: A report from the Children's Oncology Group. Pediatr Blood Cancer 66 (1): e27430, 2019. [<a href="/pmc/articles/PMC6249096/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC6249096</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/30160355" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 30160355</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_4">Malogolowkin M, Cotton CA, Green DM, et al.: Treatment of Wilms tumor relapsing after initial treatment with vincristine, actinomycin D, and doxorubicin. A report from the National Wilms Tumor Study Group. Pediatr Blood Cancer 50 (2): 236-41, 2008. [<a href="https://pubmed.ncbi.nlm.nih.gov/17539021" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 17539021</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_5">Reinhard H, Schmidt A, Furtwängler R, et al.: Outcome of relapses of nephroblastoma in patients registered in the SIOP/GPOH trials and studies. Oncol Rep 20 (2): 463-7, 2008. [<a href="https://pubmed.ncbi.nlm.nih.gov/18636212" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 18636212</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_6">Grundy P, Breslow N, Green DM, et al.: Prognostic factors for children with recurrent Wilms' tumor: results from the Second and Third National Wilms' Tumor Study. J Clin Oncol 7 (5): 638-47, 1989. [<a href="https://pubmed.ncbi.nlm.nih.gov/2540289" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 2540289</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_7">Green DM, Cotton CA, Malogolowkin M, et al.: Treatment of Wilms tumor relapsing after initial treatment with vincristine and actinomycin D: a report from the National Wilms Tumor Study Group. Pediatr Blood Cancer 48 (5): 493-9, 2007. [<a href="https://pubmed.ncbi.nlm.nih.gov/16547940" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 16547940</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_8">Warmann SW, Furtwängler R, Blumenstock G, et al.: Tumor biology influences the prognosis of nephroblastoma patients with primary pulmonary metastases: results from SIOP 93-01/GPOH and SIOP 2001/GPOH. Ann Surg 254 (1): 155-62, 2011. [<a href="https://pubmed.ncbi.nlm.nih.gov/21670612" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 21670612</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_9">Dome JS, Cotton CA, Perlman EJ, et al.: Treatment of anaplastic histology Wilms' tumor: results from the fifth National Wilms' Tumor Study. J Clin Oncol 24 (15): 2352-8, 2006. [<a href="https://pubmed.ncbi.nlm.nih.gov/16710034" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 16710034</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_10">Shamberger RC, Anderson JR, Breslow NE, et al.: Long-term outcomes for infants with very low risk Wilms tumor treated with surgery alone in National Wilms Tumor Study-5. Ann Surg 251 (3): 555-8, 2010. [<a href="/pmc/articles/PMC2836016/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC2836016</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/20142733" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 20142733</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_11">Abu-Ghosh AM, Krailo MD, Goldman SC, et al.: Ifosfamide, carboplatin and etoposide in children with poor-risk relapsed Wilms' tumor: a Children's Cancer Group report. Ann Oncol 13 (3): 460-9, 2002. [<a href="https://pubmed.ncbi.nlm.nih.gov/11996479" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 11996479</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_12">Garaventa A, Hartmann O, Bernard JL, et al.: Autologous bone marrow transplantation for pediatric Wilms' tumor: the experience of the European Bone Marrow Transplantation Solid Tumor Registry. Med Pediatr Oncol 22 (1): 11-4, 1994. [<a href="https://pubmed.ncbi.nlm.nih.gov/8232074" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 8232074</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_13">Pein F, Michon J, Valteau-Couanet D, et al.: High-dose melphalan, etoposide, and carboplatin followed by autologous stem-cell rescue in pediatric high-risk recurrent Wilms' tumor: a French Society of Pediatric Oncology study. J Clin Oncol 16 (10): 3295-301, 1998. [<a href="https://pubmed.ncbi.nlm.nih.gov/9779704" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 9779704</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_14">Rossoff J, Tse WT, Duerst RE, et al.: High-dose chemotherapy and autologous hematopoietic stem-cell rescue for treatment of relapsed and refractory Wilms tumor: Re-evaluating outcomes. Pediatr Hematol Oncol 35 (5-6): 316-321, 2018 Aug - Sep. [<a href="https://pubmed.ncbi.nlm.nih.gov/30681039" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 30681039</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_15">Malogolowkin MH, Hemmer MT, Le-Rademacher J, et al.: Outcomes following autologous hematopoietic stem cell transplant for patients with relapsed Wilms' tumor: a CIBMTR retrospective analysis. Bone Marrow Transplant 52 (11): 1549-1555, 2017. [<a href="/pmc/articles/PMC5665725/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC5665725</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/28869618" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 28869618</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_16">Seibel NL, Chi YY, Perlman EJ, et al.: Impact of cyclophosphamide and etoposide on outcome of clear cell sarcoma of the kidney treated on the National Wilms Tumor Study-5 (NWTS-5). Pediatr Blood Cancer 66 (1): e27450, 2019. [<a href="/pmc/articles/PMC6249042/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC6249042</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/30255545" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 30255545</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_17">Gooskens SL, Furtwängler R, Spreafico F, et al.: Treatment and outcome of patients with relapsed clear cell sarcoma of the kidney: a combined SIOP and AIEOP study. Br J Cancer 111 (2): 227-33, 2014. [<a href="/pmc/articles/PMC4102945/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC4102945</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/24937667" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 24937667</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_18">Radulescu VC, Gerrard M, Moertel C, et al.: Treatment of recurrent clear cell sarcoma of the kidney with brain metastasis. Pediatr Blood Cancer 50 (2): 246-9, 2008. [<a href="https://pubmed.ncbi.nlm.nih.gov/17226850" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 17226850</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_19">Gooskens SL, Houwing ME, Vujanic GM, et al.: Congenital mesoblastic nephroma 50 years after its recognition: A narrative review. Pediatr Blood Cancer 64 (7): , 2017. [<a href="https://pubmed.ncbi.nlm.nih.gov/28124468" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 28124468</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_20">Drilon A, Laetsch TW, Kummar S, et al.: Efficacy of Larotrectinib in TRK Fusion-Positive Cancers in Adults and Children. N Engl J Med 378 (8): 731-739, 2018. [<a href="/pmc/articles/PMC5857389/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC5857389</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/29466156" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 29466156</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_108_21">Entrectinib Shows Pediatric Potential. Cancer Discov 9 (7): OF4, 2019. [<a href="https://pubmed.ncbi.nlm.nih.gov/31113803" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 31113803</span></a>]</div></li></ol></div></div><div id="CDR0000062789__1820"><h2 id="_CDR0000062789__1820_">Special Considerations for the Treatment of Children With Cancer</h2><p id="CDR0000062789__1821">Cancer in children and adolescents is rare, although the overall incidence of childhood cancer has been slowly increasing since 1975.[<a class="bk_pop" href="#CDR0000062789_rl_1820_1">1</a>] Children and adolescents with
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cancer need to be referred to medical centers that have multidisciplinary teams
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of cancer specialists with experience treating the cancers that occur during
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childhood and adolescence. This multidisciplinary team approach incorporates
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the skills of the following health care professionals and others to ensure that children receive treatment, supportive care, and rehabilitation that will achieve optimal survival and quality of life:</p><ul id="CDR0000062789__1827"><li class="half_rhythm"><div>Primary care physicians.</div></li><li class="half_rhythm"><div>Pediatric surgical subspecialists.</div></li><li class="half_rhythm"><div>Radiation oncologists.</div></li><li class="half_rhythm"><div>Pediatric medical oncologists/hematologists.</div></li><li class="half_rhythm"><div>Rehabilitation specialists.</div></li><li class="half_rhythm"><div>Pediatric nurse specialists.</div></li><li class="half_rhythm"><div>Social workers.</div></li></ul><p id="CDR0000062789__1832">
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Refer to the PDQ summaries on <a href="https://www.cancer.gov/publications/pdq/information-summaries/supportive-care" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Supportive and Palliative Care</a> for specific information about supportive care for children and adolescents with cancer.</p><p id="CDR0000062789__1822">Guidelines for pediatric cancer centers and their role in the treatment of
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pediatric patients with cancer have been outlined by the American Academy of
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Pediatrics.[<a class="bk_pop" href="#CDR0000062789_rl_1820_2">2</a>] At these pediatric cancer centers, clinical trials are
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available for most of the types of cancer that occur in children and
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adolescents, and the opportunity to participate in these trials is offered to
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most patients and their families. Clinical trials for children and adolescents with
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cancer are generally designed to compare potentially better therapy with
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therapy that is currently accepted as standard. Most of the progress
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made in identifying curative therapies for childhood cancers has been achieved
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through clinical trials under the auspices of cooperative groups such as the <a href="https://childrensoncologygroup.org/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Children's Oncology Group</a> (COG) and the <a href="https://siop-online.org/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">International Society of Pediatric Oncology</a> (SIOP). Information about ongoing clinical trials is
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available from the <a href="https://www.cancer.gov/about-cancer/treatment/clinical-trials" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">NCI website</a>. </p><div id="CDR0000062789_rl_1820"><h3>References</h3><ol><li><div class="bk_ref" id="CDR0000062789_rl_1820_1">Smith MA, Seibel NL, Altekruse SF, et al.: Outcomes for children and adolescents with cancer: challenges for the twenty-first century. J Clin Oncol 28 (15): 2625-34, 2010. [<a href="/pmc/articles/PMC2881732/" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pmc">PMC free article<span class="bk_prnt">: PMC2881732</span></a>] [<a href="https://pubmed.ncbi.nlm.nih.gov/20404250" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 20404250</span></a>]</div></li><li><div class="bk_ref" id="CDR0000062789_rl_1820_2">Corrigan JJ, Feig SA; American Academy of Pediatrics: Guidelines for pediatric cancer centers. Pediatrics 113 (6): 1833-5, 2004. [<a href="https://pubmed.ncbi.nlm.nih.gov/15173520" ref="pagearea=cite-ref&targetsite=entrez&targetcat=link&targettype=pubmed">PubMed<span class="bk_prnt">: 15173520</span></a>]</div></li></ol></div></div><div id="CDR0000062789__134"><h2 id="_CDR0000062789__134_">Changes to This Summary (11/05/2020)</h2><p id="CDR0000062789__137">The PDQ cancer information summaries are reviewed regularly and updated as
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new information becomes available. This section describes the latest
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changes made to this summary as of the date above.</p><p id="CDR0000062789__1983">This summary was reformatted.</p><p id="CDR0000062789__disclaimerHP_3">This summary is written and maintained by the <a href="https://www.cancer.gov/publications/pdq/editorial-boards/pediatric-treatment" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PDQ Pediatric Treatment Editorial Board</a>, which is
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editorially independent of NCI. The summary reflects an independent review of
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the literature and does not represent a policy statement of NCI or NIH. More
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information about summary policies and the role of the PDQ Editorial Boards in
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maintaining the PDQ summaries can be found on the <a href="#CDR0000062789__AboutThis_1">About This PDQ Summary</a> and <a href="https://www.cancer.gov/publications/pdq" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PDQ® - NCI's Comprehensive Cancer Database</a> pages.
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</p></div><div id="CDR0000062789__AboutThis_1"><h2 id="_CDR0000062789__AboutThis_1_">About This PDQ Summary</h2><div id="CDR0000062789__AboutThis_2"><h3>Purpose of This Summary</h3><p id="CDR0000062789__AboutThis_3">This PDQ cancer information summary for health professionals provides comprehensive, peer-reviewed, evidence-based information about the treatment of Wilms tumor and other childhood kidney tumors. It is intended as a resource to inform and assist clinicians who care for cancer patients. It does not provide formal guidelines or recommendations for making health care decisions.</p></div><div id="CDR0000062789__AboutThis_4"><h3>Reviewers and Updates</h3><p id="CDR0000062789__AboutThis_5">This summary is reviewed regularly and updated as necessary by the <a href="https://www.cancer.gov/publications/pdq/editorial-boards/pediatric-treatment" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">PDQ Pediatric Treatment Editorial Board</a>, which is editorially independent of the National Cancer Institute (NCI). The summary reflects an independent review of the literature and does not represent a policy statement of NCI or the National Institutes of Health (NIH).</p><p id="CDR0000062789__AboutThis_22"> Board members review recently published articles each month to determine whether an article should:</p><ul id="CDR0000062789__AboutThis_6"><li class="half_rhythm"><div>be discussed at a meeting,</div></li><li class="half_rhythm"><div>be cited with text, or</div></li><li class="half_rhythm"><div>replace or update an existing article that is already cited.</div></li></ul><p id="CDR0000062789__AboutThis_7">Changes to the summaries are made through a consensus process in which Board members evaluate the strength of the evidence in the published articles and determine how the article should be included in the summary.</p><p>The lead reviewers for Wilms Tumor and Other Childhood Kidney Tumors Treatment are:</p><ul><li class="half_rhythm"><div>Louis S. Constine, MD (James P. Wilmot Cancer Center at University of Rochester Medical Center)</div></li><li class="half_rhythm"><div>Christopher N. Frantz, MD (Alfred I. duPont Hospital for Children)</div></li><li class="half_rhythm"><div>Andrea A. Hayes-Jordan, MD, FACS, FAAP (University of North Carolina - Chapel Hill School of Medicine)</div></li><li class="half_rhythm"><div>Nita Louise Seibel, MD (National Cancer Institute)</div></li><li class="half_rhythm"><div>Stephen J. Shochat, MD (St. Jude Children's Research Hospital)</div></li></ul><p id="CDR0000062789__AboutThis_9">Any comments or questions about the summary content should be submitted to Cancer.gov through the NCI website's <a href="https://www.cancer.gov/contact/email-us" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Email Us</a>. Do not contact the individual Board Members with questions or comments about the summaries. Board members will not respond to individual inquiries.</p></div><div id="CDR0000062789__AboutThis_10"><h3>Levels of Evidence</h3><p id="CDR0000062789__AboutThis_11">Some of the reference citations in this summary are accompanied by a level-of-evidence designation. These designations are intended to help readers assess the strength of the evidence supporting the use of specific interventions or approaches. The PDQ Pediatric Treatment Editorial Board uses a <a href="/books/n/pdqcis/CDR0000062796/">formal evidence ranking system</a> in developing its level-of-evidence designations.</p></div><div id="CDR0000062789__AboutThis_12"><h3>Permission to Use This Summary</h3><p id="CDR0000062789__AboutThis_13">PDQ is a registered trademark. Although the content of PDQ documents can be used freely as text, it cannot be identified as an NCI PDQ cancer information summary unless it is presented in its entirety and is regularly updated. However, an author would be permitted to write a sentence such as “NCI’s PDQ cancer information summary about breast cancer prevention states the risks succinctly: [include excerpt from the summary].”</p><p id="CDR0000062789__AboutThis_14">The preferred citation for this PDQ summary is:</p><p id="CDR0000062789__AboutThis_15">PDQ® Pediatric Treatment Editorial Board. PDQ Wilms Tumor and Other Childhood Kidney Tumors Treatment. Bethesda, MD: National Cancer Institute. Updated <MM/DD/YYYY>. Available at: <a href="https://www.cancer.gov/types/kidney/hp/wilms-treatment-pdq" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">https://www.cancer.gov/types/kidney/hp/wilms-treatment-pdq</a>. Accessed <MM/DD/YYYY>. [PMID: 26389282]</p><p id="CDR0000062789__AboutThis_16">Images in this summary are used with permission of the author(s), artist, and/or publisher for use within the PDQ summaries only. Permission to use images outside the context of PDQ information must be obtained from the owner(s) and cannot be granted by the National Cancer Institute. Information about using the illustrations in this summary, along with many other cancer-related images, is available in <a href="https://visualsonline.cancer.gov/" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Visuals Online</a>, a collection of over 2,000 scientific images.
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</p></div><div id="CDR0000062789__AboutThis_17"><h3>Disclaimer</h3><p id="CDR0000062789__AboutThis_18">Based on the strength of the available evidence, treatment options may be described as either “standard” or “under clinical evaluation.” These classifications should not be used as a basis for insurance reimbursement determinations. More information on insurance coverage is available on Cancer.gov on the <a href="https://www.cancer.gov/about-cancer/managing-care" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Managing Cancer Care</a> page.</p></div><div id="CDR0000062789__AboutThis_20"><h3>Contact Us</h3><p id="CDR0000062789__AboutThis_21">More information about contacting us or receiving help with the Cancer.gov website can be found on our <a href="https://www.cancer.gov/contact" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Contact Us for Help</a> page. Questions can also be submitted to Cancer.gov through the website’s <a href="https://www.cancer.gov/contact/email-us" ref="pagearea=body&targetsite=external&targetcat=link&targettype=uri">Email Us</a>.</p></div></div></div></div>
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<div class="post-content"><div><div class="half_rhythm"><a href="/books/about/copyright/">Copyright Notice</a></div><div class="small"><span class="label">Bookshelf ID: NBK65842</span><span class="label">PMID: <a href="https://pubmed.ncbi.nlm.nih.gov/26389282" title="PubMed record of this page" ref="pagearea=meta&targetsite=entrez&targetcat=link&targettype=pubmed">26389282</a></span></div></div></div>
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<div xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"></div><div class="portlet"><div class="portlet_head"><div class="portlet_title"><h3><span>Views</span></h3></div><a name="Shutter" sid="1" href="#" class="portlet_shutter" title="Show/hide content" remembercollapsed="true" pgsec_name="PDF_download" id="Shutter"></a></div><div class="portlet_content"><ul xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="simple-list"><li><a href="/books/NBK65842.23/?report=reader">PubReader</a></li><li><a href="/books/NBK65842.23/?report=printable">Print View</a></li><li><a data-jig="ncbidialog" href="#_ncbi_dlg_citbx_NBK65842" data-jigconfig="width:400,modal:true">Cite this Page</a><div id="_ncbi_dlg_citbx_NBK65842" style="display:none" title="Cite this Page"><div class="bk_tt">PDQ Pediatric Treatment Editorial Board. Wilms Tumor and Other Childhood Kidney Tumors Treatment (PDQ®): Health Professional Version. 2020 Nov 5. In: PDQ Cancer Information Summaries [Internet]. 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2015</li></ul></div></div><div class="portlet"><div class="portlet_head"><div class="portlet_title"><h3><span>In this Page</span></h3></div><a name="Shutter" sid="1" href="#" class="portlet_shutter" title="Show/hide content" remembercollapsed="true" pgsec_name="page-toc" id="Shutter"></a></div><div class="portlet_content"><ul xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="simple-list"><li><a href="#CDR0000062789__755" ref="log$=inpage&link_id=inpage">General Information About Childhood Kidney Tumors</a></li><li><a href="#CDR0000062789__1" ref="log$=inpage&link_id=inpage">Wilms Tumor</a></li><li><a href="#CDR0000062789__432" ref="log$=inpage&link_id=inpage">Renal Cell Carcinoma (RCC)</a></li><li><a href="#CDR0000062789__17" ref="log$=inpage&link_id=inpage">Rhabdoid Tumors of the Kidney</a></li><li><a href="#CDR0000062789__10" ref="log$=inpage&link_id=inpage">Clear Cell Sarcoma of the Kidney</a></li><li><a href="#CDR0000062789__429" ref="log$=inpage&link_id=inpage">Congenital Mesoblastic Nephroma</a></li><li><a href="#CDR0000062789__20" ref="log$=inpage&link_id=inpage">Ewing Sarcoma of the Kidney </a></li><li><a href="#CDR0000062789__1241" ref="log$=inpage&link_id=inpage">Primary Renal Myoepithelial Carcinoma</a></li><li><a href="#CDR0000062789__150" ref="log$=inpage&link_id=inpage">Cystic Partially Differentiated Nephroblastoma </a></li><li><a href="#CDR0000062789__383" ref="log$=inpage&link_id=inpage">Multilocular Cystic Nephroma</a></li><li><a href="#CDR0000062789__438" ref="log$=inpage&link_id=inpage">Primary Renal Synovial Sarcoma</a></li><li><a href="#CDR0000062789__440" ref="log$=inpage&link_id=inpage">Anaplastic Sarcoma of the Kidney</a></li><li><a href="#CDR0000062789__436" ref="log$=inpage&link_id=inpage">Nephroblastomatosis </a></li><li><a href="#CDR0000062789__108" ref="log$=inpage&link_id=inpage">Treatment of Recurrent Childhood Kidney Tumors</a></li><li><a href="#CDR0000062789__1820" ref="log$=inpage&link_id=inpage">Special Considerations for the Treatment of Children With Cancer</a></li><li><a href="#CDR0000062789__134" ref="log$=inpage&link_id=inpage">Changes to This Summary (11/05/2020)</a></li><li><a href="#CDR0000062789__AboutThis_1" ref="log$=inpage&link_id=inpage">About This PDQ Summary</a></li></ul></div></div><div class="portlet"><div class="portlet_head"><div class="portlet_title"><h3><span>Related publications</span></h3></div><a name="Shutter" sid="1" href="#" class="portlet_shutter" title="Show/hide content" remembercollapsed="true" pgsec_name="document-links" id="Shutter"></a></div><div class="portlet_content"><ul xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="simple-list"><li><a href="/books/NBK65953/">Patient Version</a></li></ul></div></div><div class="portlet"><div class="portlet_head"><div class="portlet_title"><h3><span>Related 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pgsec_name="PBooksDiscovery_RA" id="Shutter"></a></div><div class="portlet_content"><ul><li class="brieflinkpopper two_line"><a class="brieflinkpopperctrl" href="/pubmed/26389390" ref="ordinalpos=1&linkpos=1&log$=relatedreviews&logdbfrom=pubmed"><span xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="invert">Review</span> Wilms Tumor and Other Childhood Kidney Tumors Treatment (PDQ®): Patient Version.</a><span class="source">[PDQ Cancer Information Summari...]</span><div class="brieflinkpop offscreen_noflow"><span xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="invert">Review</span> Wilms Tumor and Other Childhood Kidney Tumors Treatment (PDQ®): Patient Version.<div class="brieflinkpopdesc"><em xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="author">PDQ Pediatric Treatment Editorial Board. </em><em xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="cit">PDQ Cancer Information Summaries. 2002</em></div></div></li><li class="brieflinkpopper two_line"><a class="brieflinkpopperctrl" href="/pubmed/26389426" ref="ordinalpos=1&linkpos=2&log$=relatedreviews&logdbfrom=pubmed"><span xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="invert">Review</span> Childhood Central Nervous System Atypical Teratoid/Rhabdoid Tumor Treatment (PDQ®): Health Professional Version.</a><span class="source">[PDQ Cancer Information Summari...]</span><div class="brieflinkpop offscreen_noflow"><span xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="invert">Review</span> Childhood Central Nervous System Atypical Teratoid/Rhabdoid Tumor Treatment (PDQ®): Health Professional Version.<div class="brieflinkpopdesc"><em xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="author">PDQ Pediatric Treatment Editorial Board. </em><em xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="cit">PDQ Cancer Information Summaries. 2002</em></div></div></li><li class="brieflinkpopper two_line"><a class="brieflinkpopperctrl" href="/pubmed/26389232" ref="ordinalpos=1&linkpos=3&log$=relatedreviews&logdbfrom=pubmed"><span xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="invert">Review</span> Childhood Liver Cancer Treatment (PDQ®): Health Professional Version.</a><span class="source">[PDQ Cancer Information Summari...]</span><div class="brieflinkpop offscreen_noflow"><span xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="invert">Review</span> Childhood Liver Cancer Treatment (PDQ®): Health Professional Version.<div class="brieflinkpopdesc"><em xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="author">PDQ Pediatric Treatment Editorial Board. </em><em xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="cit">PDQ Cancer Information Summaries. 2002</em></div></div></li><li class="brieflinkpopper two_line"><a class="brieflinkpopperctrl" href="/pubmed/26389373" ref="ordinalpos=1&linkpos=4&log$=relatedreviews&logdbfrom=pubmed"><span xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="invert">Review</span> Childhood Ependymoma Treatment (PDQ®): Health Professional Version.</a><span class="source">[PDQ Cancer Information Summari...]</span><div class="brieflinkpop offscreen_noflow"><span xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="invert">Review</span> Childhood Ependymoma Treatment (PDQ®): Health Professional Version.<div class="brieflinkpopdesc"><em xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="author">PDQ Pediatric Treatment Editorial Board. </em><em xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="cit">PDQ Cancer Information Summaries. 2002</em></div></div></li><li class="brieflinkpopper two_line"><a class="brieflinkpopperctrl" href="/pubmed/26389330" ref="ordinalpos=1&linkpos=5&log$=relatedreviews&logdbfrom=pubmed"><span xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="invert">Review</span> Childhood Craniopharyngioma Treatment (PDQ®): Health Professional Version.</a><span class="source">[PDQ Cancer Information Summari...]</span><div class="brieflinkpop offscreen_noflow"><span xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="invert">Review</span> Childhood Craniopharyngioma Treatment (PDQ®): Health Professional Version.<div class="brieflinkpopdesc"><em xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="author">PDQ Pediatric Treatment Editorial Board. </em><em xmlns:np="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" class="cit">PDQ Cancer Information Summaries. 2002</em></div></div></li></ul><a class="seemore" href="/sites/entrez?db=pubmed&cmd=link&linkname=pubmed_pubmed_reviews&uid=26389282" ref="ordinalpos=1&log$=relatedreviews_seeall&logdbfrom=pubmed">See reviews...</a><a class="seemore" href="/sites/entrez?db=pubmed&cmd=link&linkname=pubmed_pubmed&uid=26389282" ref="ordinalpos=1&log$=relatedarticles_seeall&logdbfrom=pubmed">See all...</a></div></div><div class="portlet"><div 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