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Enfortumab Vedotin and Pembrolizumab in Untreated Advanced Urothelial Cancer
DC Field | Value | Language |
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dc.contributor.author | 신상준 | - |
dc.date.accessioned | 2025-02-03T08:51:38Z | - |
dc.date.available | 2025-02-03T08:51:38Z | - |
dc.date.issued | 2024-03 | - |
dc.identifier.issn | 0028-4793 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/201936 | - |
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.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Massachusetts Medical Society | - |
dc.relation.isPartOf | NEW ENGLAND JOURNAL OF MEDICINE | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Antibodies, Monoclonal* / administration & dosage | - |
dc.subject.MESH | Antibodies, Monoclonal* / adverse effects | - |
dc.subject.MESH | Antibodies, Monoclonal* / therapeutic use | - |
dc.subject.MESH | Antibodies, Monoclonal, Humanized / administration & dosage | - |
dc.subject.MESH | Antibodies, Monoclonal, Humanized / adverse effects | - |
dc.subject.MESH | Antibodies, Monoclonal, Humanized / therapeutic use | - |
dc.subject.MESH | Antineoplastic Agents* / administration & dosage | - |
dc.subject.MESH | Antineoplastic Agents* / adverse effects | - |
dc.subject.MESH | Antineoplastic Agents* / therapeutic use | - |
dc.subject.MESH | Carboplatin / administration & dosage | - |
dc.subject.MESH | Carboplatin / adverse effects | - |
dc.subject.MESH | Carboplatin / therapeutic use | - |
dc.subject.MESH | Carcinoma, Transitional Cell* / drug therapy | - |
dc.subject.MESH | Carcinoma, Transitional Cell* / pathology | - |
dc.subject.MESH | Carcinoma, Transitional Cell* / secondary | - |
dc.subject.MESH | Cisplatin / administration & dosage | - |
dc.subject.MESH | Cisplatin / adverse effects | - |
dc.subject.MESH | Cisplatin / therapeutic use | - |
dc.subject.MESH | Gemcitabine / administration & dosage | - |
dc.subject.MESH | Gemcitabine / adverse effects | - |
dc.subject.MESH | Gemcitabine / therapeutic use | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Survival Analysis | - |
dc.subject.MESH | Urinary Bladder Neoplasms | - |
dc.subject.MESH | Urologic Neoplasms* / drug therapy | - |
dc.subject.MESH | Urologic Neoplasms* / pathology | - |
dc.subject.MESH | Urologic Neoplasms* / secondary | - |
dc.title | Enfortumab Vedotin and Pembrolizumab in Untreated Advanced Urothelial Cancer | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
dc.contributor.googleauthor | Thomas Powles | - |
dc.contributor.googleauthor | Begoña P Valderrama | - |
dc.contributor.googleauthor | Shilpa Gupta | - |
dc.contributor.googleauthor | Jens Bedke | - |
dc.contributor.googleauthor | Eiji Kikuchi | - |
dc.contributor.googleauthor | Jean Hoffman-Censits | - |
dc.contributor.googleauthor | Gopa Iyer | - |
dc.contributor.googleauthor | Christof Vulsteke | - |
dc.contributor.googleauthor | Se Hoon Park | - |
dc.contributor.googleauthor | Sang Joon Shin | - |
dc.contributor.googleauthor | Daniel Castellano | - |
dc.contributor.googleauthor | Giuseppe Fornarini | - |
dc.contributor.googleauthor | Jian-Ri Li | - |
dc.contributor.googleauthor | Mahmut Gümüş | - |
dc.contributor.googleauthor | Nataliya Mar | - |
dc.contributor.googleauthor | Yohann Loriot | - |
dc.contributor.googleauthor | Aude Fléchon | - |
dc.contributor.googleauthor | Ignacio Duran | - |
dc.contributor.googleauthor | Alexandra Drakaki | - |
dc.contributor.googleauthor | Sujata Narayanan | - |
dc.contributor.googleauthor | Xuesong Yu | - |
dc.contributor.googleauthor | Seema Gorla | - |
dc.contributor.googleauthor | Blanca Homet Moreno | - |
dc.contributor.googleauthor | Michiel S van der Heijden | - |
dc.contributor.googleauthor | EV-302 Trial Investigators | - |
dc.identifier.doi | 10.1056/NEJMoa2312117 | - |
dc.contributor.localId | A02105 | - |
dc.relation.journalcode | J02371 | - |
dc.identifier.eissn | 1533-4406 | - |
dc.identifier.pmid | 38446675 | - |
dc.identifier.url | https://www.nejm.org/doi/10.1056/NEJMoa2312117 | - |
dc.contributor.alternativeName | Shin, Sang Joon | - |
dc.contributor.affiliatedAuthor | 신상준 | - |
dc.citation.volume | 390 | - |
dc.citation.number | 10 | - |
dc.citation.startPage | 875 | - |
dc.citation.endPage | 888 | - |
dc.identifier.bibliographicCitation | NEW ENGLAND JOURNAL OF MEDICINE, Vol.390(10) : 875-888, 2024-03 | - |
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