Enfortumab vedotin and pembrolizumab: redefining the standard of care for previously untreated advanced urothelial cancer

被引:0
作者
Sternschuss, Michal [1 ,2 ]
Rosenberg, Jonathan E. [1 ,3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Genitourinary Oncol Serv Chief, 353 East 68th St, New York, NY 10065 USA
[2] Rabin Med Ctr, Davidoff Canc Ctr, Petah Tiqwa, Israel
[3] Weill Cornell Med Coll, Dept Med, New York, NY USA
关键词
Enfortumab vedotin; pembrolizumab; urothelial carcinoma; antibody-drug conjugate; immune checkpoint inhibitor; CISPLATIN-INELIGIBLE PATIENTS; TRANSITIONAL-CELL CARCINOMA; GEMCITABINE PLUS CISPLATIN; PHASE-II TRIAL; CHEMOTHERAPY; KEYNOTE-052; PLATINUM; MULTICENTER; NECTIN-4; OUTCOMES;
D O I
10.1080/14796694.2025.2482363
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Combination treatment with Enfortumab vedotin (EV), an antibody drug conjugate targeting Nectin-4 with a monomethyl auristatin E (MMAE) payload, and pembrolizumab, a programmed death 1 (PD-1) inhibitor, has become the new standard of care for previously untreated locally advanced or metastatic urothelial carcinoma. In the recently published phase III study, EV-302, EV and pembrolizumab demonstrated improved outcomes compared to platinum-based chemotherapy, including objective response rate, progression free survival, and an unprecedented median overall survival of 33.8 months (versus 15.9 months; hazard ratio for death 0.51; 95% confidence interval 0.43-0.61; p < 0.00001). We reviewed the mechanism of action, clinical efficacy, exploratory biomarkers, and safety profile of EV and pembrolizumab as monotherapies and combination in urothelial cancer.
引用
收藏
页码:1333 / 1348
页数:16
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