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

dc.contributor.authorO’Donnell, Peter H.
dc.contributor.authorLoriot, Yohann
dc.contributor.authorCsoszi, Tibor
dc.contributor.authorMatsubara, Nobuaki
dc.contributor.authorShin, Sang Joon
dc.contributor.authorPark, Se Hoon
dc.contributor.authorAtduev, Vagif
dc.date.accessioned2025-05-10T15:23:59Z
dc.date.issued2025
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractBackground: First-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. Methods: Patients 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. Results: A 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. Conclusions: Frontline 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. © 2024 The Author(s). Cancer published by Wiley Periodicals LLC on behalf of American Cancer Society.
dc.description.sponsorshipMerck Sharp & Dohme LLC
dc.identifier.doi10.1002/cncr.35601
dc.identifier.issn0008-543X
dc.identifier.issue1
dc.identifier.pmid39465550
dc.identifier.scopus2-s2.0-85207950555
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1002/cncr.35601
dc.identifier.urihttps://hdl.handle.net/20.500.14730/6572
dc.identifier.volume131
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofCancer
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_Scopus_20250302
dc.subjectadvanced urothelial carcinoma; bladder cancer; immunotherapy; pembrolizumab; platinum ineligibility
dc.titleEfficacy 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
dc.typeArticle

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