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.authorid | 0000-0003-4478-7282 | |
| dc.authorid | 0000-0001-5350-7241 | |
| dc.contributor.author | Matsubara, Nobuaki | |
| dc.contributor.author | de Wit, Ronald | |
| dc.contributor.author | Balar, Arjun Vasant | |
| dc.contributor.author | Siefker-Radtke, Arlene O. | |
| dc.contributor.author | Zolnierek, Jakub | |
| dc.contributor.author | Csoszi, Tibor | |
| dc.contributor.author | Shin, Sang Joon | |
| dc.date.accessioned | 2025-05-10T19:49:25Z | |
| dc.date.issued | 2024 | |
| dc.department | İstanbul Medeniyet Üniversitesi | |
| dc.description.abstract | Background: 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.sponsorship | Merck Sharp Dohme LLC | |
| dc.description.sponsorship | The 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.doi | 10.1016/j.eururo.2023.08.012 | |
| dc.identifier.endpage | 238 | |
| dc.identifier.issn | 0302-2838 | |
| dc.identifier.issn | 1873-7560 | |
| dc.identifier.issue | 3 | |
| dc.identifier.pmid | 37778952 | |
| dc.identifier.scopus | 2-s2.0-85172986667 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 229 | |
| dc.identifier.uri | https://doi.org/10.1016/j.eururo.2023.08.012 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14730/12027 | |
| dc.identifier.volume | 85 | |
| dc.identifier.wos | WOS:001203252600001 | |
| dc.identifier.wosquality | Q1 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | PubMed | |
| dc.language.iso | en | |
| dc.publisher | Elsevier | |
| dc.relation.ispartof | European Urology | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.snmz | KA_WOS_20250302 | |
| dc.subject | Bladder cancer | |
| dc.subject | Checkpoint inhibitor | |
| dc.subject | Cisplatin Ineligible | |
| dc.subject | Immunotherapy | |
| dc.subject | Lenvatinib | |
| dc.subject | Pembrolizumab | |
| dc.subject | Platinum ineligible | |
| dc.title | 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.type | Article |
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