Enfortumab Vedotin and Pembrolizumab in Untreated Advanced Urothelial Cancer

dc.authorid0000-0003-2775-0293
dc.authorid0000-0002-4607-5660
dc.contributor.authorPowles, T.
dc.contributor.authorValderrama, B. P.
dc.contributor.authorGupta, S.
dc.contributor.authorBedke, J.
dc.contributor.authorKikuchi, E.
dc.contributor.authorHoffman-Censits, J.
dc.contributor.authorIyer, G.
dc.date.accessioned2025-05-10T19:44:33Z
dc.date.issued2024
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractBackground 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.sponsorshipAstellas Pharma US; Merck Sharp and Dohme; Merck; Seagen
dc.description.sponsorshipSupported by Astellas Pharma US; Merck Sharp and Dohme, a subsidiary of Merck; and Seagen, which was acquired by Pfizer in December 2023
dc.identifier.doi10.1056/NEJMoa2312117
dc.identifier.endpage888
dc.identifier.issn0028-4793
dc.identifier.issn1533-4406
dc.identifier.issue10
dc.identifier.pmid38446675
dc.identifier.scopus2-s2.0-85187199941
dc.identifier.scopusqualityQ1
dc.identifier.startpage875
dc.identifier.urihttps://doi.org/10.1056/NEJMoa2312117
dc.identifier.urihttps://hdl.handle.net/20.500.14730/10974
dc.identifier.volume390
dc.identifier.wosWOS:001184386500010
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherMassachusetts Medical Soc
dc.relation.ispartofNew England Journal of Medicine
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectCisplatin-Ineligible Patients
dc.subjectTreatment Patterns
dc.subjectOpen-Label
dc.subjectChemotherapy
dc.subjectMulticenter
dc.subjectSurvival
dc.subjectTherapy
dc.titleEnfortumab Vedotin and Pembrolizumab in Untreated Advanced Urothelial Cancer
dc.typeArticle

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