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Enfortumab Vedotin and Pembrolizumab in Untreated Advanced Urothelial Cancer

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dc.contributor.author신상준-
dc.date.accessioned2025-02-03T08:51:38Z-
dc.date.available2025-02-03T08:51:38Z-
dc.date.issued2024-03-
dc.identifier.issn0028-4793-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/201936-
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.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherMassachusetts Medical Society-
dc.relation.isPartOfNEW ENGLAND JOURNAL OF MEDICINE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAntibodies, Monoclonal* / administration & dosage-
dc.subject.MESHAntibodies, Monoclonal* / adverse effects-
dc.subject.MESHAntibodies, Monoclonal* / therapeutic use-
dc.subject.MESHAntibodies, Monoclonal, Humanized / administration & dosage-
dc.subject.MESHAntibodies, Monoclonal, Humanized / adverse effects-
dc.subject.MESHAntibodies, Monoclonal, Humanized / therapeutic use-
dc.subject.MESHAntineoplastic Agents* / administration & dosage-
dc.subject.MESHAntineoplastic Agents* / adverse effects-
dc.subject.MESHAntineoplastic Agents* / therapeutic use-
dc.subject.MESHCarboplatin / administration & dosage-
dc.subject.MESHCarboplatin / adverse effects-
dc.subject.MESHCarboplatin / therapeutic use-
dc.subject.MESHCarcinoma, Transitional Cell* / drug therapy-
dc.subject.MESHCarcinoma, Transitional Cell* / pathology-
dc.subject.MESHCarcinoma, Transitional Cell* / secondary-
dc.subject.MESHCisplatin / administration & dosage-
dc.subject.MESHCisplatin / adverse effects-
dc.subject.MESHCisplatin / therapeutic use-
dc.subject.MESHGemcitabine / administration & dosage-
dc.subject.MESHGemcitabine / adverse effects-
dc.subject.MESHGemcitabine / therapeutic use-
dc.subject.MESHHumans-
dc.subject.MESHSurvival Analysis-
dc.subject.MESHUrinary Bladder Neoplasms-
dc.subject.MESHUrologic Neoplasms* / drug therapy-
dc.subject.MESHUrologic Neoplasms* / pathology-
dc.subject.MESHUrologic Neoplasms* / secondary-
dc.titleEnfortumab Vedotin and Pembrolizumab in Untreated Advanced Urothelial Cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorThomas Powles-
dc.contributor.googleauthorBegoña P Valderrama-
dc.contributor.googleauthorShilpa Gupta-
dc.contributor.googleauthorJens Bedke-
dc.contributor.googleauthorEiji Kikuchi-
dc.contributor.googleauthorJean Hoffman-Censits-
dc.contributor.googleauthorGopa Iyer-
dc.contributor.googleauthorChristof Vulsteke-
dc.contributor.googleauthorSe Hoon Park-
dc.contributor.googleauthorSang Joon Shin-
dc.contributor.googleauthorDaniel Castellano-
dc.contributor.googleauthorGiuseppe Fornarini-
dc.contributor.googleauthorJian-Ri Li-
dc.contributor.googleauthorMahmut Gümüş-
dc.contributor.googleauthorNataliya Mar-
dc.contributor.googleauthorYohann Loriot-
dc.contributor.googleauthorAude Fléchon-
dc.contributor.googleauthorIgnacio Duran-
dc.contributor.googleauthorAlexandra Drakaki-
dc.contributor.googleauthorSujata Narayanan-
dc.contributor.googleauthorXuesong Yu-
dc.contributor.googleauthorSeema Gorla-
dc.contributor.googleauthorBlanca Homet Moreno-
dc.contributor.googleauthorMichiel S van der Heijden-
dc.contributor.googleauthorEV-302 Trial Investigators-
dc.identifier.doi10.1056/NEJMoa2312117-
dc.contributor.localIdA02105-
dc.relation.journalcodeJ02371-
dc.identifier.eissn1533-4406-
dc.identifier.pmid38446675-
dc.identifier.urlhttps://www.nejm.org/doi/10.1056/NEJMoa2312117-
dc.contributor.alternativeNameShin, Sang Joon-
dc.contributor.affiliatedAuthor신상준-
dc.citation.volume390-
dc.citation.number10-
dc.citation.startPage875-
dc.citation.endPage888-
dc.identifier.bibliographicCitationNEW ENGLAND JOURNAL OF MEDICINE, Vol.390(10) : 875-888, 2024-03-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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