Wong Risa L, Yu Evan Y
University of Pittsburgh, 4200 Fifth Ave, Pittsburgh, PA 15260, USA.
UPMC Hillman Cancer Center, 5115 Centre Ave, Pittsburgh, PA 15232, USA.
Future Oncol. 2022 Sep;18(27):3067-3084. doi: 10.2217/fon-2022-0328. Epub 2022 Aug 25.
Enfortumab vedotin (EV) is the first antibody-drug conjugate approved for locally advanced or metastatic urothelial cancers (la/mUCs), a disease group historically associated with limited prognosis and therapeutic options. EV consists of monomethyl auristatin E, a microtubule-disrupting agent linked to an antibody targeting Nectin-4. In clinical trials, EV demonstrated high response rates and superior survival in the third-line setting for la/mUC compared with chemotherapy. Peripheral neuropathy and rash were among the most common serious adverse events. EV is currently approved in multiple countries for the treatment of la/mUC in the later-line setting. Ongoing trials seek to expand the indication for EV and to study therapeutic combinations with other agents.
恩杂鲁胺(Enfortumab vedotin,EV)是首个被批准用于局部晚期或转移性尿路上皮癌(la/mUC)的抗体药物偶联物,该疾病组历来预后有限且治疗选择不多。EV由单甲基奥瑞他汀E组成,这是一种与靶向Nectin-4的抗体相连的微管破坏剂。在临床试验中,与化疗相比,EV在la/mUC的三线治疗中显示出高缓解率和更好的生存率。周围神经病变和皮疹是最常见的严重不良事件。目前,EV已在多个国家被批准用于后线治疗la/mUC。正在进行的试验旨在扩大EV的适应症,并研究与其他药物的联合治疗。