2020
DOI: 10.1177/1756287220980192
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Enfortumab Vedotin in urothelial cancer

Abstract: The treatment landscape for metastatic urothelial cancer (mUC) beyond first-line platinum-based chemotherapy has changed significantly over the last 5 years with the recent approvals of the immune checkpoint inhibitors (ICIs), fibroblast growth factor receptor (FGFR) inhibitors and most recently Enfortumab Vedotin (EV). EV is a novel antibody–drug conjugate (ADC), that delivers monomethyl auristatin E (MMAE), a microtubule-disrupting agent, inside cells harboring the cell surface nectin-4 receptor. In mUC, EV … Show more

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Cited by 26 publications
(22 citation statements)
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“…Enfortumab vedotin is composed of a fully human monoclonal antibody against nectin-4, a type I transmembrane cell adhesion protein that is highly expressed in a number of epithelial cancers, including urothelial cancer, and monomethyl auristatin E, an anti-cancer agent that disrupts microtubule formation in cancer cells ( 8 ). The ADC is a new type of anti-cancer agent, and the linker plays the important role of attaching the monoclonal antibody to the cytotoxic agent ( 32 , 33 ). The linker is stable in the bloodstream and releases the drug into the cells only after binding to the target.…”
Section: Urothelial Cancermentioning
confidence: 99%
“…Enfortumab vedotin is composed of a fully human monoclonal antibody against nectin-4, a type I transmembrane cell adhesion protein that is highly expressed in a number of epithelial cancers, including urothelial cancer, and monomethyl auristatin E, an anti-cancer agent that disrupts microtubule formation in cancer cells ( 8 ). The ADC is a new type of anti-cancer agent, and the linker plays the important role of attaching the monoclonal antibody to the cytotoxic agent ( 32 , 33 ). The linker is stable in the bloodstream and releases the drug into the cells only after binding to the target.…”
Section: Urothelial Cancermentioning
confidence: 99%
“…This is a humanized anti-trophoblast cell-surface antigen 2 (Trop 2) antibody, conjugated with SN-38, an active metabolite of irinotecan that inhibits the nuclear topoisomerase 1, inducing double-stranded DNA breaks and, ultimately, cell death. 54 , 55 …”
Section: Subsequent Lines Of Therapymentioning
confidence: 99%
“…Because nectin-4 is highly expressed in all metastatic UC tumors, once the bonded enfortumab vedotin is internalized, the microtubule-disrupting agent MMAE is released leading to apoptosis of the tumor cell. Clinical trials demonstrated enfortumab vedotin is a new therapeutic method in patients with platinum-and immune checkpoint inhibitor-refractory disease (70,71).…”
Section: Bladder Cancer Genomics and Precision Treatmentmentioning
confidence: 99%