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Enfortumab Vedotin and Pembrolizumab in Untreated Advanced Urothelial Cancer

Authors
 Powles, T.  ;  Valderrama, B. P.  ;  Gupta, S.  ;  Bedke, J.  ;  Kikuchi, E.  ;  Hoffman-Censits, J.  ;  Iyer, G.  ;  Vulsteke, C.  ;  Park, S. H.  ;  Shin, S. J.  ;  Castellano, D.  ;  Fornarini, G.  ;  Li, J. R.  ;  Guemues, M.  ;  Mar, N.  ;  Loriot, Y.  ;  Flechon, A.  ;  Duran, I  ;  Drakaki, A.  ;  Narayanan, S.  ;  Yu, X.  ;  Gorla, S.  ;  Moreno, B. Homet  ;  van der Heijden, M. S. 
Citation
 NEW ENGLAND JOURNAL OF MEDICINE, Vol.390(10) : 875-888, 2024-03 
Journal Title
NEW ENGLAND JOURNAL OF MEDICINE
ISSN
 0028-4793 
Issue Date
2024-03
Abstract
Background No treatment has surpassed platinum-based chemotherapy in improving overall survival in patients with previously untreated locally advanced or metastatic urothelial carcinoma. Methods We conducted a phase 3, global, open-label, randomized trial to compare the efficacy and safety of enfortumab vedotin and pembrolizumab with the efficacy and safety of platinum-based chemotherapy in patients with previously untreated locally advanced or metastatic urothelial carcinoma. Patients were randomly assigned in a 1:1 ratio to receive 3-week cycles of enfortumab vedotin (at a dose of 1.25 mg per kilogram of body weight intravenously on days 1 and 8) and pembrolizumab (at a dose of 200 mg intravenously on day 1) (enfortumab vedotin-pembrolizumab group) or gemcitabine and either cisplatin or carboplatin (determined on the basis of eligibility to receive cisplatin) (chemotherapy group). The primary end points were progression-free survival as assessed by blinded independent central review and overall survival. Results A total of 886 patients underwent randomization: 442 to the enfortumab vedotin-pembrolizumab group and 444 to the chemotherapy group. As of August 8, 2023, the median duration of follow-up for survival was 17.2 months. Progression-free survival was longer in the enfortumab vedotin-pembrolizumab group than in the chemotherapy group (median, 12.5 months vs. 6.3 months; hazard ratio for disease progression or death, 0.45; 95% confidence interval [CI], 0.38 to 0.54; P<0.001), as was overall survival (median, 31.5 months vs. 16.1 months; hazard ratio for death, 0.47; 95% CI, 0.38 to 0.58; P<0.001). The median number of cycles was 12 (range, 1 to 46) in the enfortumab vedotin-pembrolizumab group and 6 (range, 1 to 6) in the chemotherapy group. Treatment-related adverse events of grade 3 or higher occurred in 55.9% of the patients in the enfortumab vedotin-pembrolizumab group and in 69.5% of those in the chemotherapy group. Conclusions Treatment with enfortumab vedotin and pembrolizumab resulted in significantly better outcomes than chemotherapy in patients with untreated locally advanced or metastatic urothelial carcinoma, with a safety profile consistent with that in previous reports. (Funded by Astellas Pharma US and others; EV-302 ClinicalTrials.gov number, NCT04223856.)
DOI
10.1056/NEJMoa2312117
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Shin, Sang Joon(신상준) ORCID logo https://orcid.org/0000-0001-5350-7241
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/201936
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