The use of tafasitamab in diffuse large B-cell lymphoma
- PMID: 34285786
- PMCID: PMC8264734
- DOI: 10.1177/20406207211027458
The use of tafasitamab in diffuse large B-cell lymphoma
Abstract
Patients who relapse or are refractory after first-line therapy for diffuse large B-cell lymphoma (DLBCL) frequently have poor prognoses, especially when they are not candidates for autologous stem cell transplant (ASCT). Tafasitamab is a humanized monoclonal anti-CD19 antibody that has recently been approved by the FDA in combination with lenalidomide for the treatment of relapsed/refractory (R/R) DLBCL in patients who are not eligible for ASCT. Tafasitamab has an Fc region which has been modified to have an increased affinity for Fcγ receptors, to potentiate antibody-dependent cellular cytotoxicity and antibody-dependent cell-mediated phagocytosis. Here, we review the development, mode of action and clinical data for tafasitamab in combination with lenalidomide in R/R DLBCL, and discuss the various ways in which this novel antibody could be utilized in the treatment sequence to improve clinical outcomes for patients with DLBCL.
Keywords: DLBCL; anti-CD19; clinical data; diffuse large B-cell lymphoma; lenalidomide; mode of action; monoclonal antibody; real-world evidence; tafasitamab.
© The Author(s), 2021.
Conflict of interest statement
Conflict of interest statement: GS reports non-financial support from MorphoSys, during the conduct of the study; other from MorphoSys, other from BMS, other from AbbVieˇ, other from Janssen, other from Merck, other from Novartis, other from Gilead/Kite, other from Epizyme, other from Celgene/BMS, other from Roche/Genentech, other from Takeda, other from Autolus, other from Genmab, other from Velosbio, outside the submitted work; in addition, GS has a patent WO2012010561A1 issued. MT has nothing to disclose. JD reports non-financial support from MorphoSys, during the conduct of the study.
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