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Efficacy and safety of pembrolizumab in patients with advanced urothelial carcinoma deemed potentially ineligible for platinum-containing chemotherapy: Post hoc analysis of KEYNOTE-052 and LEAP-011

Authors
 O'Donnell, Peter H.  ;  Loriot, Yohann  ;  Csoszi, Tibor  ;  Matsubara, Nobuaki  ;  Shin, Sang Joon  ;  Park, Se Hoon  ;  Atduev, Vagif  ;  Gumus, Mahmut  ;  Karaca, Saziye Burcak  ;  Grivas, Petros  ;  de Wit, Ronald  ;  Castellano, Daniel E.  ;  Powles, Thomas  ;  Vuky, Jacqueline  ;  Zhao, Yujie  ;  O'Hara, Karen  ;  Okpara, Chinyere E.  ;  Franco, Sonia  ;  Moreno, Blanca Homet  ;  Zolnierek, Jakub  ;  Siefker-Radtke, Arlene O. 
Citation
 CANCER, Vol.131(1), 2025-01 
Article Number
 e35601 
Journal Title
CANCER
ISSN
 0008-543X 
Issue Date
2025-01
Keywords
advanced urothelial carcinoma ; bladder cancer ; immunotherapy ; pembrolizumab ; platinum ineligibility
Abstract
BackgroundFirst-line pembrolizumab monotherapy is a standard of care for platinum-ineligible patients with advanced urothelial carcinoma (UC). No global standardized definition of platinum ineligibility exists. This study aimed to evaluate the efficacy and safety of pembrolizumab monotherapy in patients with UC who met various criteria for platinum ineligibility.MethodsPatients from KEYNOTE-052 and LEAP-011 deemed potentially platinum ineligible were pooled for this post hoc exploratory analysis as follows: group 1: Eastern Cooperative Oncology Group performance status (ECOG PS) 2; group 2: ECOG PS 2 and age >= 80 years, renal dysfunction, or visceral disease; and group 3: any two other factors regardless of ECOG PS. Patients received pembrolizumab 200 mg intravenously every 3 weeks. End points included objective response rate (ORR), progression-free survival (PFS) per Response Evaluation Criteria in Solid Tumors, version 1.1, by blinded independent central review, overall survival (OS), and safety.ResultsA total of 612 patients treated with pembrolizumab from KEYNOTE-052 (n = 370) and LEAP-011 (n = 242) were included; the median (range) follow-up was 56.3 months (51.2-65.3 months) and 12.8 months (0.2-25.1 months), respectively. For group 1, ORR was 26.2%, median PFS was 2.7 months, and median OS was 10.1 months. For group 2, ORR ranged from 23.5% to 33.3%, median PFS ranged from 2.1 to 4.4 months, and median OS ranged from 9.1 to 10.1 months. For group 3, ORR ranged from 25.7% to 27.9%, median PFS ranged from 2.1 to 2.8 months, and median OS ranged from 9.0 to 10.6 months. Treatment-related adverse event rates were consistent across groups.ConclusionsFrontline pembrolizumab has consistent antitumor activity and safety in patients with advanced UC categorized as potentially ineligible for platinum-based chemotherapy, regardless of the variable definitions of platinum ineligibility used.
DOI
10.1002/cncr.35601
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Shin, Sang Joon(신상준) ORCID logo https://orcid.org/0000-0001-5350-7241
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/209035
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