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<meta name="keywords" content="CN077967, braf, cetuximab response, egfr, erbb2, erbitux response, kras, nras, sign or symptom, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="Cetuximab is a monoclonal antibody used in the treatment of metastatic colorectal cancer (mCRC) and cancer of the head and neck. Cetuximab is an epidermal growth factor receptor (EGFR) antagonist, which works by blocking the growth of cancer cells. It is administered as a weekly intravenous (IV) infusion, but in practice, is often given every other week to coincide with chemotherapy (for example, FOLFIRI or FOLFOX). Cetuximab has several off-label uses as well, which include non-small cell lung cancer, squamous cell carcinoma of the skin, and Menetriers disease. Interestingly, for colorectal cancer, the location of the primary tumor influences whether an individual with mCRC will respond to anti-EGFR therapy, and influences prognosis. Individuals with left-sided tumors are more likely to respond well to anti-EGFR therapy and have a better prognosis. Individuals with right-sided tumors have a worse prognosis and respond poorly to anti-EGFR therapy. However, currently only the mutation status of the tumor, and not the location of the tumor, is discussed in the drug labels dosing recommendations. Resistance to cetuximab is associated with specific RAS mutations. The RAS family of oncogenes includes the KRAS and NRAS genes. When mutated, these genes have the ability to transform normal cells into cancerous cells. The KRAS mutations are particularly common, being detectable in 40% of metastatic colorectal tumors. The KRAS mutations often lead to constitutive activation of the mitogen-activated protein kinase (MAPK) pathway and are associated with resistance to anti-EGFR drugs such as cetuximab. In addition, mutations in NRAS and another gene, BRAF, have been associated with poor response to anti-EGFR therapy; however, BRAF mutation does not explicitly preclude anti-EGFR therapy. Combination therapies targeting both BRAF and EGFR have shown to improve survival for individuals with wild-type RAS and mutant BRAF. The 2018 FDA-approved drug label for cetuximab states that for mCRC, cetuximab is indicated for K- and N-RAS wild-type (no mutation), EGFR-expressing tumors. The label states that an FDA-approved test must be used to confirm the absence of a RAS mutation (in either KRAS or NRAS) prior to starting cetuximab. While the FDA label also states that EGFR expression should also be confirmed by an approved test prior to starting therapy for mCRC, this is largely not implemented in practice, nor is it recommended by professional oncology society guidelines. Similarly, the 2015 Update from the American Society of Clinical Oncology (ASCO) states that anti-EGFR therapy should only be considered for the treatment of individuals whose tumor is determined to not have mutations detected after extended RAS testing. The 2020 National Comprehensive Cancer Network (NCCN) guideline also strongly recommends KRAS/NRAS genotyping of tumor tissue in all individuals with mCRC. In addition, the guideline states the V600E mutation in the BRAF gene makes a response to cetuximab (and panitumumab) highly unlikely unless given a BRAF inhibitor." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
UID=450439
ConceptID=CN077967
-->
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Cetuximab response</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>450439</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier assigned by MedGen (starting with CN) for terms&#10;that cannot be identified in NLM's Unified Medical Language system (UMLS)&#10;Click for more information."><span class="highlight" style="background-color:">CN077967</span></a></dd><dt><span class="dotprefix"></span></dt><dd>Sign or Symptom</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
<td>Erbitux response</td></tr>
<tr><td>Drug:</td>
<td>
<div class="divPopper rprt" id="drug_242381"><div><strong>Cetuximab</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>242381</dd><dt><span class="dotprefix"></span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS)&#10;Click for more information.">C0995188</a></dd><dt><span class="dotprefix"></span></dt><dd>Pharmacologic Substance</dd></dl></div></div></div>
<div class="spaceAbove">A recombinant, chimeric monoclonal antibody directed against the epidermal growth factor (EGFR) with antineoplastic activity. Cetuximab binds to the extracellular domain of the EGFR, thereby preventing the activation and subsequent dimerization of the receptor; the decrease in receptor activation and dimerization may result in an inhibition in signal transduction and anti-proliferative effects. This agent may inhibit EGFR-dependent primary tumor growth and metastasis. EGFR is overexpressed on the cell surfaces of various solid tumors. [from NCI]</div></div>
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#drug_242381" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cetuximab</a></div></td></tr>
<tr><td colspan="2" class="small"> </td></tr><tr><td><a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#target-gene-loc">Genes (locations):<img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a><div class="display-none" id="target-gene-loc">
Gene(s) directly associated with<br />
this condition or phenotype.</div></td>
<td><a target="_blank" title="BRAF - ID: 673 - NCBI Gene" href="/gene/673" class="medgenPMinfo">BRAF</a> (7q34); <a target="_blank" title="EGFR - ID: 1956 - NCBI Gene" href="/gene/1956" class="medgenPMinfo">EGFR</a> (7p11.2); <a target="_blank" title="ERBB2 - ID: 2064 - NCBI Gene" href="/gene/2064" class="medgenPMinfo">ERBB2</a> (17q12); <a target="_blank" title="KRAS - ID: 3845 - NCBI Gene" href="/gene/3845" class="medgenPMinfo">KRAS</a> (12p12.1); <a target="_blank" title="NRAS - ID: 4893 - NCBI Gene" href="/gene/4893" class="medgenPMinfo">NRAS</a> (1p13.2)</td></tr>
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<div class="portlet mgSection" id="ID_100">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln">Cetuximab is a monoclonal antibody used in the treatment of metastatic colorectal cancer (mCRC) and cancer of the head and neck. Cetuximab is an epidermal growth factor receptor (EGFR) antagonist, which works by blocking the growth of cancer cells. It is administered as a weekly intravenous (IV) infusion, but in practice, is often given every other week to coincide with chemotherapy (for example, FOLFIRI or FOLFOX). Cetuximab has several off-label uses as well, which include non-small cell lung cancer, squamous cell carcinoma of the skin, and Menetriers disease. Interestingly, for colorectal cancer, the location of the primary tumor influences whether an individual with mCRC will respond to anti-EGFR therapy, and influences prognosis. Individuals with left-sided tumors are more likely to respond well to anti-EGFR therapy and have a better prognosis. Individuals with right-sided tumors have a worse prognosis and respond poorly to anti-EGFR therapy. However, currently only the mutation status of the tumor, and not the location of the tumor, is discussed in the drug labels dosing recommendations. Resistance to cetuximab is associated with specific RAS mutations. The RAS family of oncogenes includes the KRAS and NRAS genes. When mutated, these genes have the ability to transform normal cells into cancerous cells. The KRAS mutations are particularly common, being detectable in 40% of metastatic colorectal tumors. The KRAS mutations often lead to constitutive activation of the mitogen-activated protein kinase (MAPK) pathway and are associated with resistance to anti-EGFR drugs such as cetuximab. In addition, mutations in NRAS and another gene, BRAF, have been associated with poor response to anti-EGFR therapy; however, BRAF mutation does not explicitly preclude anti-EGFR therapy. Combination therapies targeting both BRAF and EGFR have shown to improve survival for individuals with wild-type RAS and mutant BRAF. The 2018 FDA-approved drug label for cetuximab states that for mCRC, cetuximab is indicated for K- and N-RAS wild-type (no mutation), EGFR-expressing tumors. The label states that an FDA-approved test must be used to confirm the absence of a RAS mutation (in either KRAS or NRAS) prior to starting cetuximab. While the FDA label also states that EGFR expression should also be confirmed by an approved test prior to starting therapy for mCRC, this is largely not implemented in practice, nor is it recommended by professional oncology society guidelines. Similarly, the 2015 Update from the American Society of Clinical Oncology (ASCO) states that anti-EGFR therapy should only be considered for the treatment of individuals whose tumor is determined to not have mutations detected after extended RAS testing. The 2020 National Comprehensive Cancer Network (NCCN) guideline also strongly recommends KRAS/NRAS genotyping of tumor tissue in all individuals with mCRC. In addition, the guideline states the V600E mutation in the BRAF gene makes a response to cetuximab (and panitumumab) highly unlikely unless given a BRAF inhibitor. [from <a title="Medical Genetics Summaries" href="https://www.ncbi.nlm.nih.gov/books/NBK61999" class="defSource" target="_blank">Medical Genetics Summaries</a>]</div>
</div>
<div class="portlet mgSection" id="ID_105">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
<div class="nl"><a target="_blank" href="/pubmed/36252154">Treatment of Metastatic Colorectal Cancer: ASCO Guideline.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Morris VK,
Kennedy EB,
Baxter NN,
Benson AB 3rd,
Cercek A,
Cho M,
Ciombor KK,
Cremolini C,
Davis A,
Deming DA,
Fakih MG,
Gholami S,
Hong TS,
Jaiyesimi I,
Klute K,
Lieu C,
Sanoff H,
Strickler JH,
White S,
Willis JA,
Eng C</span><br />
<span class="medgenPMjournal">J Clin Oncol</span>
2023 Jan 20;41(3):678-700.
Epub 2022 Oct 17
doi: 10.1200/JCO.22.01690.
<span class="bold">PMID: </span><a href="/pubmed/36252154" target="_blank">36252154</a><a href="/pmc/articles/PMC10506310" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34278747">An overview of diagnosis and management of drug-induced hypomagnesemia.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Liamis G,
Hoorn EJ,
Florentin M,
Milionis H</span><br />
<span class="medgenPMjournal">Pharmacol Res Perspect</span>
2021 Aug;9(4):e00829.
doi: 10.1002/prp2.829.
<span class="bold">PMID: </span><a href="/pubmed/34278747" target="_blank">34278747</a><a href="/pmc/articles/PMC8287009" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/33591350">Diagnosis and Treatment of Metastatic Colorectal Cancer: A Review.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Biller LH,
Schrag D</span><br />
<span class="medgenPMjournal">JAMA</span>
2021 Feb 16;325(7):669-685.
doi: 10.1001/jama.2021.0106.
<span class="bold">PMID: </span><a href="/pubmed/33591350" target="_blank">33591350</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22cetuximab%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (844)</a></div><h3 class="subhead">Curated<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpCurated"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3><h3 class="nl vspace"><a href="https://www.nccn.org/professionals/physician_gls/pdf/head-and-neck.pdf" target="_blank">NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®), Head and Neck Cancers, 2024</a></h3>
<h3 class="nl vspace"><a href="https://www.nccn.org/professionals/physician_gls/pdf/colon.pdf" target="_blank">NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Colon Cancer, 2024</a></h3>
<h3 class="nl vspace"><a href="https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8bc6397e-4bd8-4d37-a007-a327e4da34d9" target="_blank">DailyMed Drug Label, cetuximab, 2021</a></h3>
<h3 class="nl vspace"><a href="https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8bc6397e-4bd8-4d37-a007-a327e4da34d9" target="_blank">DailyMed Drug Label, ERBITUX, 2021</a></h3>
</div>
</div>
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
<div class="portlet mgSection" id="ID_103">
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
<div class="nl"><a target="_blank" href="/pubmed/37195126">Anna Karenina principle in personalized treatment of bladder cancer according to oncogram: which drug for which patient?</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Celik S,
Gokbayrak O,
Erol A,
Yorukoglu K,
Aktas T,
Sari H,
Yilmaz B,
Mungan MU,
Aslan G,
Celebi I,
Altun Z,
Yavuzsen T,
Aktas S</span><br />
<span class="medgenPMjournal">Per Med</span>
2023 Mar;20(2):175-182.
Epub 2023 May 17
doi: 10.2217/pme-2022-0134.
<span class="bold">PMID: </span><a href="/pubmed/37195126" target="_blank">37195126</a></div>
<div class="nl"><a target="_blank" href="/pubmed/32141150">New genetic variations discovered in KRAS wild-type cetuximab resistant chinese colorectal cancer patients.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Jing C,
Wang T,
Ma R,
Cao H,
Wang Z,
Liu S,
Chen D,
Zhang J,
Wu Y,
Zhang Y,
Wu J,
Feng J</span><br />
<span class="medgenPMjournal">Mol Carcinog</span>
2020 May;59(5):478-491.
Epub 2020 Mar 5
doi: 10.1002/mc.23172.
<span class="bold">PMID: </span><a href="/pubmed/32141150" target="_blank">32141150</a></div>
<div class="nl"><a target="_blank" href="/pubmed/30478503">The roles of PTEN, cMET, and p16 in resistance to cetuximab in head and neck squamous cell carcinoma.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">da Costa AABA,
Costa FD,
Araújo DV,
Camandaroba MPG,
de Jesus VHF,
Oliveira A,
Alves ACF,
Stecca C,
Machado L,
de Oliveira ACF,
de Oliveira TB,
Nicolau UR,
de Lima VCC</span><br />
<span class="medgenPMjournal">Med Oncol</span>
2018 Nov 26;36(1):8.
doi: 10.1007/s12032-018-1234-0.
<span class="bold">PMID: </span><a href="/pubmed/30478503" target="_blank">30478503</a></div>
<div class="nl"><a target="_blank" href="/pubmed/30463680">Cetuximab Alone or With Irinotecan for Resistant KRAS-, NRAS-, BRAF- and PIK3CA-wild-type Metastatic Colorectal Cancer: The AGITG Randomized Phase II ICECREAM Study.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Shapiro JD,
Thavaneswaran S,
Underhill CR,
Robledo KP,
Karapetis CS,
Day FL,
Nott LM,
Jefford M,
Chantrill LA,
Pavlakis N,
Tebbutt NC,
Price TJ,
Khasraw M,
Van Hazel GA,
Waring PM,
Tejpar S,
Simes J,
Gebski VJ,
Desai J,
Segelov E</span><br />
<span class="medgenPMjournal">Clin Colorectal Cancer</span>
2018 Dec;17(4):313-319.
Epub 2018 Jun 8
doi: 10.1016/j.clcc.2018.06.002.
<span class="bold">PMID: </span><a href="/pubmed/30463680" target="_blank">30463680</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28559019">IL6 is associated with response to dasatinib and cetuximab: Phase II clinical trial with mechanistic correlatives in cetuximab-resistant head and neck cancer.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Stabile LP,
Egloff AM,
Gibson MK,
Gooding WE,
Ohr J,
Zhou P,
Rothenberger NJ,
Wang L,
Geiger JL,
Flaherty JT,
Grandis JR,
Bauman JE</span><br />
<span class="medgenPMjournal">Oral Oncol</span>
2017 Jun;69:38-45.
Epub 2017 Apr 9
doi: 10.1016/j.oraloncology.2017.03.011.
<span class="bold">PMID: </span><a href="/pubmed/28559019" target="_blank">28559019</a><a href="/pmc/articles/PMC5944328" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cetuximab%20response%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (13)</a></div><h3 class="subhead">Diagnosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/39209908">XENTURION is a population-level multidimensional resource of xenografts and tumoroids from metastatic colorectal cancer patients.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Leto SM,
Grassi E,
Avolio M,
Vurchio V,
Cottino F,
Ferri M,
Zanella ER,
Borgato S,
Corti G,
di Blasio L,
Somale D,
Vara-Messler M,
Galimi F,
Sassi F,
Lupo B,
Catalano I,
Pinnelli M,
Viviani M,
Sperti L,
Mellano A,
Ferrero A,
Zingaretti CC,
Puliafito A,
Primo L,
Bertotti A,
Trusolino L</span><br />
<span class="medgenPMjournal">Nat Commun</span>
2024 Aug 29;15(1):7495.
doi: 10.1038/s41467-024-51909-2.
<span class="bold">PMID: </span><a href="/pubmed/39209908" target="_blank">39209908</a><a href="/pmc/articles/PMC11362617" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/37728512">The Inherited KRAS-variant as a Biomarker of Cetuximab Response in NSCLC.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Weidhaas JB,
Hu C,
Komaki R,
Masters GA,
Blumenschein GR,
Chang JY,
Lu B,
Dicker AP,
Bogart JA,
Garces YI,
Narayan S,
Robinson CG,
Kavadi VS,
Greenberger JS,
Koprowski CD,
Welsh J,
Gore EM,
MacRae RM,
Paulus R,
Bradley JD</span><br />
<span class="medgenPMjournal">Cancer Res Commun</span>
2023 Oct 11;3(10):2074-2081.
doi: 10.1158/2767-9764.CRC-23-0084.
<span class="bold">PMID: </span><a href="/pubmed/37728512" target="_blank">37728512</a><a href="/pmc/articles/PMC10566451" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/37119788">Establishment of patient-derived tumor organoids to functionally inform treatment decisions in metastatic colorectal cancer.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Martini G,
Belli V,
Napolitano S,
Ciaramella V,
Ciardiello D,
Belli A,
Izzo F,
Avallone A,
Selvaggi F,
Menegon Tasselli F,
Santaniello W,
Franco R,
Puig I,
Ramirez L,
Chicote I,
Mancuso F,
Caratu G,
Serres X,
Fasani R,
Jimenez J,
Ros J,
Baraibar I,
Mulet N,
Della Corte CM,
Troiani T,
Vivancos A,
Dienstmann R,
Elez E,
Palmer HG,
Tabernero J,
Martinelli E,
Ciardiello F,
Argilés G</span><br />
<span class="medgenPMjournal">ESMO Open</span>
2023 Jun;8(3):101198.
Epub 2023 Apr 27
doi: 10.1016/j.esmoop.2023.101198.
<span class="bold">PMID: </span><a href="/pubmed/37119788" target="_blank">37119788</a><a href="/pmc/articles/PMC10265597" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34779495">Expression of neurofibromin 1 in colorectal cancer and cetuximab resistance.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Tak E,
Kim M,
Cho Y,
Choi S,
Kim J,
Han B,
Kim HD,
Jang CS,
Kim JE,
Hong YS,
Kim SY,
Kim TW</span><br />
<span class="medgenPMjournal">Oncol Rep</span>
2022 Jan;47(1)
Epub 2021 Nov 15
doi: 10.3892/or.2021.8226.
<span class="bold">PMID: </span><a href="/pubmed/34779495" target="_blank">34779495</a><a href="/pmc/articles/PMC8611403" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34546978">Caveolin-1 and Sox-2 are predictive biomarkers of cetuximab response in head and neck cancer.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Bouhaddou M,
Lee RH,
Li H,
Bhola NE,
O'Keefe RA,
Naser M,
Zhu TR,
Nwachuku K,
Duvvuri U,
Olshen AB,
Roy R,
Hechmer A,
Bolen J,
Keysar SB,
Jimeno A,
Mills GB,
Vandenberg S,
Swaney DL,
Johnson DE,
Krogan NJ,
Grandis JR</span><br />
<span class="medgenPMjournal">JCI Insight</span>
2021 Oct 22;6(20)
doi: 10.1172/jci.insight.151982.
<span class="bold">PMID: </span><a href="/pubmed/34546978" target="_blank">34546978</a><a href="/pmc/articles/PMC8564908" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cetuximab%20response%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (22)</a></div><h3 class="subhead">Therapy</h3>
<div class="nl"><a target="_blank" href="/pubmed/37728512">The Inherited KRAS-variant as a Biomarker of Cetuximab Response in NSCLC.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Weidhaas JB,
Hu C,
Komaki R,
Masters GA,
Blumenschein GR,
Chang JY,
Lu B,
Dicker AP,
Bogart JA,
Garces YI,
Narayan S,
Robinson CG,
Kavadi VS,
Greenberger JS,
Koprowski CD,
Welsh J,
Gore EM,
MacRae RM,
Paulus R,
Bradley JD</span><br />
<span class="medgenPMjournal">Cancer Res Commun</span>
2023 Oct 11;3(10):2074-2081.
doi: 10.1158/2767-9764.CRC-23-0084.
<span class="bold">PMID: </span><a href="/pubmed/37728512" target="_blank">37728512</a><a href="/pmc/articles/PMC10566451" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/35011716">Comprehensive Molecular Landscape of Cetuximab Resistance in Head and Neck Cancer Cell Lines.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Gomes INF,
da Silva-Oliveira RJ,
da Silva LS,
Martinho O,
Evangelista AF,
van Helvoort Lengert A,
Leal LF,
Silva VAO,
Dos Santos SP,
Nascimento FC,
Lopes Carvalho A,
Reis RM</span><br />
<span class="medgenPMjournal">Cells</span>
2022 Jan 4;11(1)
doi: 10.3390/cells11010154.
<span class="bold">PMID: </span><a href="/pubmed/35011716" target="_blank">35011716</a><a href="/pmc/articles/PMC8750399" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34779495">Expression of neurofibromin 1 in colorectal cancer and cetuximab resistance.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Tak E,
Kim M,
Cho Y,
Choi S,
Kim J,
Han B,
Kim HD,
Jang CS,
Kim JE,
Hong YS,
Kim SY,
Kim TW</span><br />
<span class="medgenPMjournal">Oncol Rep</span>
2022 Jan;47(1)
Epub 2021 Nov 15
doi: 10.3892/or.2021.8226.
<span class="bold">PMID: </span><a href="/pubmed/34779495" target="_blank">34779495</a><a href="/pmc/articles/PMC8611403" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34546978">Caveolin-1 and Sox-2 are predictive biomarkers of cetuximab response in head and neck cancer.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Bouhaddou M,
Lee RH,
Li H,
Bhola NE,
O'Keefe RA,
Naser M,
Zhu TR,
Nwachuku K,
Duvvuri U,
Olshen AB,
Roy R,
Hechmer A,
Bolen J,
Keysar SB,
Jimeno A,
Mills GB,
Vandenberg S,
Swaney DL,
Johnson DE,
Krogan NJ,
Grandis JR</span><br />
<span class="medgenPMjournal">JCI Insight</span>
2021 Oct 22;6(20)
doi: 10.1172/jci.insight.151982.
<span class="bold">PMID: </span><a href="/pubmed/34546978" target="_blank">34546978</a><a href="/pmc/articles/PMC8564908" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28006059">The KRAS-Variant and Cetuximab Response in Head and Neck Squamous Cell Cancer: A Secondary Analysis of a Randomized Clinical Trial.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Weidhaas JB,
Harris J,
Schaue D,
Chen AM,
Chin R,
Axelrod R,
El-Naggar AK,
Singh AK,
Galloway TJ,
Raben D,
Wang D,
Matthiesen C,
Avizonis VN,
Manon RR,
Yumen O,
Nguyen-Tan PF,
Trotti A,
Skinner H,
Zhang Q,
Ferris RL,
Sidransky D,
Chung CH</span><br />
<span class="medgenPMjournal">JAMA Oncol</span>
2017 Apr 1;3(4):483-491.
doi: 10.1001/jamaoncol.2016.5478.
<span class="bold">PMID: </span><a href="/pubmed/28006059" target="_blank">28006059</a><a href="/pmc/articles/PMC5470422" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cetuximab%20response%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (33)</a></div><h3 class="subhead">Prognosis</h3>
<div class="nl"><a target="_blank" href="/pubmed/38212428">Inhibition of autocrine HGF maturation overcomes cetuximab resistance in colorectal cancer.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Jones VT,
Graves-Deal R,
Cao Z,
Bogatcheva G,
Ramirez MA,
Harmych SJ,
Higginbotham JN,
Sharma V,
Damalanka VC,
Wahoski CC,
Joshi N,
Irudayam MJ,
Roland JT,
Ayers GD,
Liu Q,
Coffey RJ,
Janetka JW,
Singh B</span><br />
<span class="medgenPMjournal">Cell Mol Life Sci</span>
2024 Jan 12;81(1):28.
doi: 10.1007/s00018-023-05071-5.
<span class="bold">PMID: </span><a href="/pubmed/38212428" target="_blank">38212428</a><a href="/pmc/articles/PMC10784391" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/35011716">Comprehensive Molecular Landscape of Cetuximab Resistance in Head and Neck Cancer Cell Lines.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Gomes INF,
da Silva-Oliveira RJ,
da Silva LS,
Martinho O,
Evangelista AF,
van Helvoort Lengert A,
Leal LF,
Silva VAO,
Dos Santos SP,
Nascimento FC,
Lopes Carvalho A,
Reis RM</span><br />
<span class="medgenPMjournal">Cells</span>
2022 Jan 4;11(1)
doi: 10.3390/cells11010154.
<span class="bold">PMID: </span><a href="/pubmed/35011716" target="_blank">35011716</a><a href="/pmc/articles/PMC8750399" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34546978">Caveolin-1 and Sox-2 are predictive biomarkers of cetuximab response in head and neck cancer.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Bouhaddou M,
Lee RH,
Li H,
Bhola NE,
O'Keefe RA,
Naser M,
Zhu TR,
Nwachuku K,
Duvvuri U,
Olshen AB,
Roy R,
Hechmer A,
Bolen J,
Keysar SB,
Jimeno A,
Mills GB,
Vandenberg S,
Swaney DL,
Johnson DE,
Krogan NJ,
Grandis JR</span><br />
<span class="medgenPMjournal">JCI Insight</span>
2021 Oct 22;6(20)
doi: 10.1172/jci.insight.151982.
<span class="bold">PMID: </span><a href="/pubmed/34546978" target="_blank">34546978</a><a href="/pmc/articles/PMC8564908" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28006059">The KRAS-Variant and Cetuximab Response in Head and Neck Squamous Cell Cancer: A Secondary Analysis of a Randomized Clinical Trial.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Weidhaas JB,
Harris J,
Schaue D,
Chen AM,
Chin R,
Axelrod R,
El-Naggar AK,
Singh AK,
Galloway TJ,
Raben D,
Wang D,
Matthiesen C,
Avizonis VN,
Manon RR,
Yumen O,
Nguyen-Tan PF,
Trotti A,
Skinner H,
Zhang Q,
Ferris RL,
Sidransky D,
Chung CH</span><br />
<span class="medgenPMjournal">JAMA Oncol</span>
2017 Apr 1;3(4):483-491.
doi: 10.1001/jamaoncol.2016.5478.
<span class="bold">PMID: </span><a href="/pubmed/28006059" target="_blank">28006059</a><a href="/pmc/articles/PMC5470422" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/26955963">Anti-EGFR Therapy: Strategies in Head and Neck Squamous Cell Carcinoma.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Oliveira-Silva RJ,
Carolina de Carvalho A,
de Souza Viana L,
Carvalho AL,
Reis RM</span><br />
<span class="medgenPMjournal">Recent Pat Anticancer Drug Discov</span>
2016;11(2):170-83.
doi: 10.2174/1574892811666160309121238.
<span class="bold">PMID: </span><a href="/pubmed/26955963" target="_blank">26955963</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cetuximab%20response%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (28)</a></div><h3 class="subhead">Clinical prediction guides</h3>
<div class="nl"><a target="_blank" href="/pubmed/38536540">Palbociclib inhibits the progression of head and neck cancer and improves the Cetuximab response under specific condition in vitro and in vivo.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Li R,
Wang Q,
Zhao Y,
Zhu Y,
Wang X</span><br />
<span class="medgenPMjournal">Mol Biol Rep</span>
2024 Mar 27;51(1):455.
doi: 10.1007/s11033-024-09423-7.
<span class="bold">PMID: </span><a href="/pubmed/38536540" target="_blank">38536540</a></div>
<div class="nl"><a target="_blank" href="/pubmed/35011716">Comprehensive Molecular Landscape of Cetuximab Resistance in Head and Neck Cancer Cell Lines.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Gomes INF,
da Silva-Oliveira RJ,
da Silva LS,
Martinho O,
Evangelista AF,
van Helvoort Lengert A,
Leal LF,
Silva VAO,
Dos Santos SP,
Nascimento FC,
Lopes Carvalho A,
Reis RM</span><br />
<span class="medgenPMjournal">Cells</span>
2022 Jan 4;11(1)
doi: 10.3390/cells11010154.
<span class="bold">PMID: </span><a href="/pubmed/35011716" target="_blank">35011716</a><a href="/pmc/articles/PMC8750399" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34779495">Expression of neurofibromin 1 in colorectal cancer and cetuximab resistance.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Tak E,
Kim M,
Cho Y,
Choi S,
Kim J,
Han B,
Kim HD,
Jang CS,
Kim JE,
Hong YS,
Kim SY,
Kim TW</span><br />
<span class="medgenPMjournal">Oncol Rep</span>
2022 Jan;47(1)
Epub 2021 Nov 15
doi: 10.3892/or.2021.8226.
<span class="bold">PMID: </span><a href="/pubmed/34779495" target="_blank">34779495</a><a href="/pmc/articles/PMC8611403" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/34546978">Caveolin-1 and Sox-2 are predictive biomarkers of cetuximab response in head and neck cancer.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Bouhaddou M,
Lee RH,
Li H,
Bhola NE,
O'Keefe RA,
Naser M,
Zhu TR,
Nwachuku K,
Duvvuri U,
Olshen AB,
Roy R,
Hechmer A,
Bolen J,
Keysar SB,
Jimeno A,
Mills GB,
Vandenberg S,
Swaney DL,
Johnson DE,
Krogan NJ,
Grandis JR</span><br />
<span class="medgenPMjournal">JCI Insight</span>
2021 Oct 22;6(20)
doi: 10.1172/jci.insight.151982.
<span class="bold">PMID: </span><a href="/pubmed/34546978" target="_blank">34546978</a><a href="/pmc/articles/PMC8564908" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div class="nl"><a target="_blank" href="/pubmed/28006059">The KRAS-Variant and Cetuximab Response in Head and Neck Squamous Cell Cancer: A Secondary Analysis of a Randomized Clinical Trial.</a></div>
<div class="portlet_content ln"><span class="medgenPMauthor">Weidhaas JB,
Harris J,
Schaue D,
Chen AM,
Chin R,
Axelrod R,
El-Naggar AK,
Singh AK,
Galloway TJ,
Raben D,
Wang D,
Matthiesen C,
Avizonis VN,
Manon RR,
Yumen O,
Nguyen-Tan PF,
Trotti A,
Skinner H,
Zhang Q,
Ferris RL,
Sidransky D,
Chung CH</span><br />
<span class="medgenPMjournal">JAMA Oncol</span>
2017 Apr 1;3(4):483-491.
doi: 10.1001/jamaoncol.2016.5478.
<span class="bold">PMID: </span><a href="/pubmed/28006059" target="_blank">28006059</a><a href="/pmc/articles/PMC5470422" target="_blank" class="PubMedFree">Free PMC Article</a></div>
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cetuximab%20response%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (31)</a></div></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Therapeutic_recommendations">Therapeutic recommendations</h1><a sid="120" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
<div class="portlet_content ln" id="therapeutic"><strong>From <a href="https://www.ncbi.nlm.nih.gov/books/NBK564547" target="_blank">Medical Genetics Summaries</a></strong><br /><div id="TheraputicContent"><div class="divPopper rprt" id="cetuximab_REF_1" style="display: none;">1. ERBITUX- cetuximab solution [package insert]. Branchburg, NJ: ImClone LLC; 2020. Available from: <a href="https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8bc6397e-4bd8-4d37-a007-a327e4da34d9" target="_blank">https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8bc6397e-4bd8-4d37-a007-a327e4da34d9</a></div><div class="divPopper rprt" id="cetuximab_REF_3" style="display: none;">3. <i>NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines). Colon Cancer: NCCN Guidelines. Version 4.2020</i>. 15 June 2020 2020]; Available from: <a href="https://www.nccn.org/guidelines/category_1#colon" target="_blank">https://www.nccn.org/guidelines/category_1#colon</a>.</div><div class="divPopper rprt" id="cetuximab_REF_2" style="display: none;">2. Allegra C.J., Rumble R.B., Hamilton S.R., Mangu P.B., et al. Extended RAS Gene Mutation Testing in Metastatic Colorectal Carcinoma to Predict Response to Anti-Epidermal Growth Factor Receptor Monoclonal Antibody Therapy: American Society of Clinical Oncology Provisional Clinical Opinion Update 2015. J Clin Oncol. 2016;34(2):17985.</div><p><b>This section contains excerpted</b>
<sup>1</sup>
<b>information on gene-based dosing recommendations. Neither this section nor other parts of this review contain the complete recommendations from the sources.</b>
</p><h2>2020 Statement from the US Food and Drug Administration (FDA)</h2><p><b>2.2 Recommended Dosage for Colorectal Cancer (CRC)</b>
</p><p>Determine EGFR-expression status using FDA-approved tests prior to initiating treatment. Also confirm the absence of a Ras mutation prior to initiation of treatment with cetuximab. Information on FDA-approved tests for the detection of K-Ras mutations in patients with metastatic CRC is available at: http://www.fda.gov/medicaldevices/productsandmedicalprocedures/invitrodiagnostics/ucm301431.htm.</p><p>[...]</p><p><b>5.7 Increased Tumor Progression, Increased Mortality, or Lack of Benefit in Patients with Ras- Mutant mCRC</b>
</p><p>Cetuximab is not indicated for the treatment of patients with CRC that harbor somatic mutations in exon 2 (codons 12 and 13), exon 3 (codons 59 and 61), and exon 4 (codons 117 and 146) of either K-Ras or N- Ras and hereafter is referred to as “Ras” or when the Ras status is unknown.</p><p>Retrospective subset analyses of Ras-mutant and wild-type populations across several randomized clinical trials, including CRYSTAL, were conducted to investigate the role of Ras mutations on the clinical effects of anti-EGFR-directed monoclonal antibodies. Use of cetuximab in patients with Ras mutations resulted in no clinical benefit with treatment related toxicity. Confirm Ras mutation status in tumor specimens prior to initiating cetuximab.</p><p><b>Please review the complete therapeutic recommendations that are located here:</b>
(<a title="click for more information" class="jig-ncbipopper s_TOP" href="#cetuximab_REF_1" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">1</a>)</p><h2>2020 Clinical Practice Guidelines in Oncology: Colon Cancer, from the National Comprehensive Cancer Network (NCCN)</h2><p><b>Version 4.2020 Discussion update in progress.</b>
</p><p>A sizable body of literature has shown that tumors with a mutation in codon 12 or 13 of exon 2 of the <i>KRAS</i> gene are essentially insensitive to cetuximab or panitumumab therapy. More recent evidence shows mutations in <i>KRAS</i> outside of exon 2 and mutations in <i>NRAS</i> are also predictive for a lack of benefit to cetuximab and panitumumab.</p><p>The panel therefore strongly recommends <i>RAS</i> (<i>KRAS/NRAS</i>) genotyping of tumor tissue (either primary tumor or metastasis) in all patients with metastatic colorectal cancer. Patients with known <i>KRAS</i> or <i>NRAS</i> mutations should not be treated with either cetuximab or panitumumab, either alone or in combination with other anticancer agents, because they have virtually no chance of benefit and the exposure to toxicity and expense cannot be justified. ASCO released a Provisional Clinical Opinion Update on extended <i>RAS</i> testing in patients with metastatic colorectal cancer (mCRC) that is consistent with the NCCN panels recommendations. A guideline on molecular biomarkers for CRC developed by the ASCP, CAP, AMP and ASCO also recommends resting consistent with the NCCN recommendations.</p><p>The recommendation for <i>RAS</i> testing, at this point, is not meant to indicate a preference regarding regimen selection in the first-line setting. Rather, this early establishment of <i>RAS</i> status is appropriate to plan for the treatment continuum, so that the information may be obtained in a non- timesensitive manner and the patient and provider can discuss the implications of a <i>RAS</i> mutation, if present, while other treatment options still exist. Note that because anti-EGFR agents have no role in the management of stage I, II, or III disease, <i>RAS</i> genotyping of colorectal cancers at these earlier stages is not recommended.</p><p><i>KRAS</i> mutations are early events in colorectal cancer formation, and therefore a very tight correlation exists between mutation status in the primary tumor and the metastases. For this reason, <i>RAS</i> genotyping can be performed on archived specimens of either the primary tumor or a metastasis. Fresh biopsies should not be obtained solely for the purpose of <i>RAS</i> genotyping unless an archived specimen from either the primary tumor or a metastasis is unavailable.</p><p>The panel recommends that <i>KRAS</i>, <i>NRAS</i>, and <i>BRAF</i> gene testing be performed only in laboratories that are certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA-88) as qualified to perform highly complex molecular pathology testing. No specific testing methodology is recommended. The three genes can be tested individually or as part of an NGS panel.</p><p>[…]</p><p>HER2 is a member of the same family of signalling kinase receptors as EGFR and has been successfully targeted in breast cancer in both the advanced and adjuvant settings. HER2 is rarely amplified/overexpressed in CRC (approximately 3% overall), but the prevalence is higher in <i>RAF/BRAF</i>-wild type tumors (reported at %5-14%). Specific molecular diagnostic methods have been proposed for HER2 testing in CRC and HER2-targeted therapies are now recommended as subsequent therapy options in patients with tumors that have HER2 overexpression. Based on this, the NCCN Guidelines recommend testing for HER2 amplifications for patients with mCRC. If the tumor is already known to have a <i>KRAS/NRAS</i> or <i>BRAF</i> mutations, HER2 testing is not required. As HER2-targeted therapies are still under investigation, enrollment in a clinical trial is encouraged.</p><p>Evidence does not support a prognostic role of HER2 overexpression. In addition to its role as a predictive marker for HER2-targeted therapy, initial results indicated HER2 amplification/overexpression may be predictive of resistance to EGFR-targeting monoclonal antibodies.</p><p><b>Please review the complete therapeutic recommendations that are located here:</b>
(<a title="click for more information" class="jig-ncbipopper s_TOP" href="#cetuximab_REF_3" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">3</a>)<b>.</b>
</p><p>2015 Provisional Clinical Opinion from the American Society of Clinical Oncology (ASCO)All patients with metastatic colorectal cancer who are candidates for anti-EGFR antibody therapy should have their tumor tested in a Clinical Laboratory Improvement Amendmentscertified laboratory for mutations in both KRAS and NRAS exons 2 (codons 12 and 13), 3 (codons 59 and 61), and 4 (codons 117 and 146). The weight of current evidence indicates that anti-EGFR MoAb therapy should only be considered for treatment of patients whose tumor is determined to not have mutations detected after such extended RAS testing.</p><p><b>Whats New and Different?</b>
</p><p>In addition to testing for mutations in KRAS exon 2 (codons 12 and 13) as recommended previously, before treatment with anti- EGFR antibody therapy, patients with mCRC should have their tumor tested for mutations in:</p><ul><li>KRAS exons 3 (codons 59 and 61) and 4 (codons 117 and 146)</li><li>NRAS exons 2 (codons 12 and 13), 3 (codons 59 and 61), and 4 (codons 117 and 146)</li></ul><p><b>Please review the complete therapeutic recommendations that are located here:</b>
(<a title="click for more information" class="jig-ncbipopper s_TOP" href="#cetuximab_REF_2" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">2</a>)</p><p><sup>1</sup>
The FDA labels specific drug formulations. We have substituted the generic names for any drug labels in this excerpt. The FDA may not have labeled all formulations containing the generic drug. Certain terms, genes and genetic variants may be corrected in accordance with nomenclature standards, where necessary. We have given the full name of abbreviations, shown in square brackets, where necessary.</p></div></div>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=CN077967%5bDISCUI%5d&amp;filter=method%3A2%5F8" target="_blank">Deletion/duplication analysis (1)</a></li>
<li><a href="/gtr/tests?term=CN077967%5bDISCUI%5d&amp;filter=method%3A1%5F3" target="_blank">Immunohistochemistry (1)</a></li>
<li><a href="/gtr/tests?term=CN077967%5bDISCUI%5d&amp;filter=method%3A2%5F17" target="_blank">Mutation scanning of the entire coding region (1)</a></li>
<li><a href="/gtr/tests?term=CN077967%5bDISCUI%5d&amp;filter=method%3A2%5F30" target="_blank">RNA analysis (1)</a></li>
<li><a href="/gtr/tests?term=CN077967%5bDISCUI%5d&amp;filter=method%3A2%5F9" target="_blank">Sequence analysis of select exons (1)</a></li>
<li><a href="/gtr/tests?term=CN077967%5bDISCUI%5d&amp;filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (1)</a></li>
<li><a href="/gtr/tests?term=CN077967%5bDISCUI%5d&amp;filter=method%3A2%5F19" target="_blank">Targeted variant analysis (4)</a></li>
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=CN077967%5bDISCUI%5d" target="_blank">See all (7)</a></total></li>
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<div class="portlet_content ln"><ul><li><a href="https://www.pharmgkb.org/chemical/PA10040" target="_blank">PharmGKB</a></li><li><a href="https://clinicaltrials.gov/search?cond=Cetuximab%20response" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22cetuximab%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul><h3 class="subhead">Curated</h3><ul class="a_poppers"><li><a target="_blank" href="https://www.nccn.org/professionals/physician_gls/pdf/head-and-neck.pdf">NCCN, 2024</a><div>NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®), Head and Neck Cancers, 2024</div></li><li><a target="_blank" href="https://www.nccn.org/professionals/physician_gls/pdf/colon.pdf">NCCN, 2024</a><div>NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Colon Cancer, 2024</div></li><li><a target="_blank" href="https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8bc6397e-4bd8-4d37-a007-a327e4da34d9">DailyMed Drug Label, 2021</a><div>DailyMed Drug Label, cetuximab, 2021</div></li><li><a target="_blank" href="https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8bc6397e-4bd8-4d37-a007-a327e4da34d9">DailyMed Drug Label, 2021</a><div>DailyMed Drug Label, ERBITUX, 2021</div></li></ul></div>
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