Pembrolizumab with or Without Lenvatinib as First-line Therapy for Patients with Advanced Urothelial Carcinoma (LEAP-011): A Phase 3, Randomized, Double-Blind Trial

dc.authorid0000-0003-4478-7282
dc.authorid0000-0001-5350-7241
dc.contributor.authorMatsubara, Nobuaki
dc.contributor.authorde Wit, Ronald
dc.contributor.authorBalar, Arjun Vasant
dc.contributor.authorSiefker-Radtke, Arlene O.
dc.contributor.authorZolnierek, Jakub
dc.contributor.authorCsoszi, Tibor
dc.contributor.authorShin, Sang Joon
dc.date.accessioned2025-05-10T19:49:25Z
dc.date.issued2024
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractBackground: Pembrolizumab plus lenvatinib has shown antitumor activity and acceptable safety in patients with platinum -refractory urothelial carcinoma (UC). Objective: To evaluate pembrolizumab plus either lenvatinib or placebo as first -line therapy for advanced UC in the phase 3 LEAP -011 study. Design, setting, and participants: Patients with advanced UC who were ineligible for cisplatin-based therapy or any platinum -based chemotherapy were enrolled. Intervention: Patients were randomly assigned (1:1) to pembrolizumab 200 mg intravenously every 3 wk plus either lenvatinib 20 mg or placebo orally once daily. Outcome measurements and statistical analysis: Dual primary endpoints were progression -free survival (PFS) and overall survival (OS). An external data monitoring committee (DMC) regularly reviewed safety and efficacy data every 3 mo. Results and limitations: Between June 25, 2019 and July 21, 2021, 487 patients were allocated to receive lenvatinib plus pembrolizumab (n = 245) or placebo plus pembrolizumab (n = 242). The median time from randomization to the data cutoff date (July 26, 2021) was 12.8 mo (interquartile range, 6.9-19.3). The median PFS was 4.5 mo in the combination arm and 4.0 mo in the pembrolizumab arm (hazard ratio [HR] 0.90 [95% confidence interval {CI} 0.72-1.14]). The median OS was 11.8 mo for the combination arm and 12.9 mo for the pembrolizumab arm (HR 1.14 [95% CI 0.87-1.48]). Grade 3- 5 adverse events attributed to trial treatment occurred in 123 of 241 patients (51%) treated with lenvatinib plus pembrolizumab and in 66 of 242 patients (27%) treated with placebo plus pembrolizumab. This trial was terminated earlier than initially planned based on recommendation from the DMC. Conclusions: The benefit -to -risk ratio for first -line lenvatinib plus pembrolizumab was not considered favorable versus pembrolizumab plus placebo as first -line therapy in patients with advanced UC. Patient summary: Lenvatinib plus pembrolizumab was not more effective than pembrolizumab plus placebo in patients with advanced urothelial carcinoma. (c) 2023 The Authors and Merck Sharp & Dohme LLC., a subsidiary of Merck & Co., Inc., Rahway, NJ, USA. Published by Elsevier B.V. on behalf of American European Association of Urology.
dc.description.sponsorshipMerck Sharp Dohme LLC
dc.description.sponsorshipThe authors thank the patients and their families and caregivers for participating in this trial, all the investigators, and site personnel. Medical writing and/or editorial assistance was provided by Robert Steger, PhD, and Matthew Grzywacz, PhD, of ApotheCom (Yardley, PA, USA) . This assistance was funded by Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA, and Eisai Inc., Nutley, NJ, USA. This study was presented at the 2022 ASCO Genitourinary Cancers Symposium on February 17-19, 2022.
dc.identifier.doi10.1016/j.eururo.2023.08.012
dc.identifier.endpage238
dc.identifier.issn0302-2838
dc.identifier.issn1873-7560
dc.identifier.issue3
dc.identifier.pmid37778952
dc.identifier.scopus2-s2.0-85172986667
dc.identifier.scopusqualityQ1
dc.identifier.startpage229
dc.identifier.urihttps://doi.org/10.1016/j.eururo.2023.08.012
dc.identifier.urihttps://hdl.handle.net/20.500.14730/12027
dc.identifier.volume85
dc.identifier.wosWOS:001203252600001
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofEuropean Urology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectBladder cancer
dc.subjectCheckpoint inhibitor
dc.subjectCisplatin Ineligible
dc.subjectImmunotherapy
dc.subjectLenvatinib
dc.subjectPembrolizumab
dc.subjectPlatinum ineligible
dc.titlePembrolizumab with or Without Lenvatinib as First-line Therapy for Patients with Advanced Urothelial Carcinoma (LEAP-011): A Phase 3, Randomized, Double-Blind Trial
dc.typeArticle

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