Enfortumab Vedotin and Pembrolizumab in Untreated Advanced Urothelial Cancer
| dc.authorid | 0000-0003-2775-0293 | |
| dc.authorid | 0000-0002-4607-5660 | |
| dc.contributor.author | Powles, T. | |
| dc.contributor.author | Valderrama, B. P. | |
| dc.contributor.author | Gupta, S. | |
| dc.contributor.author | Bedke, J. | |
| dc.contributor.author | Kikuchi, E. | |
| dc.contributor.author | Hoffman-Censits, J. | |
| dc.contributor.author | Iyer, G. | |
| dc.date.accessioned | 2025-05-10T19:44:33Z | |
| dc.date.issued | 2024 | |
| dc.department | İstanbul Medeniyet Üniversitesi | |
| dc.description.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.) | |
| dc.description.sponsorship | Astellas Pharma US; Merck Sharp and Dohme; Merck; Seagen | |
| dc.description.sponsorship | Supported by Astellas Pharma US; Merck Sharp and Dohme, a subsidiary of Merck; and Seagen, which was acquired by Pfizer in December 2023 | |
| dc.identifier.doi | 10.1056/NEJMoa2312117 | |
| dc.identifier.endpage | 888 | |
| dc.identifier.issn | 0028-4793 | |
| dc.identifier.issn | 1533-4406 | |
| dc.identifier.issue | 10 | |
| dc.identifier.pmid | 38446675 | |
| dc.identifier.scopus | 2-s2.0-85187199941 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 875 | |
| dc.identifier.uri | https://doi.org/10.1056/NEJMoa2312117 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14730/10974 | |
| dc.identifier.volume | 390 | |
| dc.identifier.wos | WOS:001184386500010 | |
| dc.identifier.wosquality | Q1 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | PubMed | |
| dc.language.iso | en | |
| dc.publisher | Massachusetts Medical Soc | |
| dc.relation.ispartof | New England Journal of Medicine | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.snmz | KA_WOS_20250302 | |
| dc.subject | Cisplatin-Ineligible Patients | |
| dc.subject | Treatment Patterns | |
| dc.subject | Open-Label | |
| dc.subject | Chemotherapy | |
| dc.subject | Multicenter | |
| dc.subject | Survival | |
| dc.subject | Therapy | |
| dc.title | Enfortumab Vedotin and Pembrolizumab in Untreated Advanced Urothelial Cancer | |
| dc.type | Article |










