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Pembrolizumab as First-line Therapy in Cisplatin-ineligible Advanced Urothelial Cancer (KEYNOTE-052): Outcomes in Older Patients by Age and Performance Status

  • Petros Grivas
  • , Elizabeth R. Plimack
  • , Arjun V. Balar
  • , Daniel Castellano
  • , Peter H. O'Donnell
  • , Joaquim Bellmunt
  • , Thomas Powles
  • , Noah M. Hahn
  • , Ronald de Wit
  • , Dean F. Bajorin
  • , Misoo C. Ellison
  • , Tara L. Frenkl
  • , James L. Godwin
  • , Jacqueline Vuky
  • University of Washington
  • New York University
  • Hospital Universitario 12 de Octubre
  • University of Chicago
  • Harvard University
  • Queen Mary University of London
  • Johns Hopkins University
  • Erasmus University Rotterdam
  • Memorial Sloan-Kettering Cancer Center
  • Merck & Co.
  • Oregon Health and Science University

Research output: Contribution to journalArticlepeer-review

43 Scopus citations

Abstract

BACKGROUND: Patients with treatment-naive advanced urothelial cancer (UC) ineligible for cisplatin-based chemotherapy are typically older and have comorbidities, representing a difficult-to-treat population. OBJECTIVE: To evaluate the safety and antitumor activity of first-line pembrolizumab in subgroups of cisplatin-ineligible older patients (aged ≥65 and ≥75 yr) with advanced UC in KEYNOTE-052 (NCT02335424), including those with poor performance status (Eastern Cooperative Oncology Group performance status score 2 [ECOG PS2]). DESIGN, SETTING, AND PARTICIPANTS: Patients were cisplatin ineligible, had treatment-naive, histologically/cytologically confirmed, locally advanced/metastatic UC with measurable disease (Response Evaluation Criteria in Solid Tumors version 1.1 [RECIST v1.1]), and had ECOG PS0-2. Patient subgroups analyzed were aged ≥65yr (n = 302), ≥75 yr (n = 179), ≥65yr with ECOG PS2 (≥65yr+ECOG PS2; n = 119), and ≥75 yr+ECOG PS2 (n = 78). INTERVENTION: All patients received pembrolizumab 200mg intravenously every 3 wk until confirmed progression, intolerable toxicity, patient withdrawal, or 24 mo of therapy. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: The primary endpoint was objective response rate (ORR) as per RECIST v1.1. The key secondary endpoints were overall survival (OS), duration of response (DOR), and safety. RESULTS AND LIMITATIONS: ORRs for the ≥65yr, ≥75 yr, ≥65yr+ECOG PS2, and ≥75 yr+ECOG PS2 subgroups were 29%, 27%, 29%, and 31%, respectively; rates of complete and partial responses were similar across subgroups (9%, 5%, 6%, and 6%, and 20%, 22%, 23%, and 24%, respectively). Median DOR and OS were also consistent across the ≥65yr and ≥65yr+ECOG PS2 subgroups and the ≥75 yr and ≥75 yr+ECOG PS2 subgroups. Study limitations included open-label design, lack of a comparator group, and nature of post hoc exploratory analysis. CONCLUSIONS: The clinical benefit of pembrolizumab in advanced UC appeared to be consistent regardless of age and/or poor performance status. PATIENT SUMMARY: This study looked at whether older age and poorer performance status affect how well patients with previously untreated advanced urothelial cancer ineligible for standard-of-care treatment respond to pembrolizumab. Outcomes with pembrolizumab were not affected by older age or poorer performance status, making it an effective option.

Original languageEnglish
Pages (from-to)351-359
Number of pages9
JournalEuropean urology oncology
Volume3
Issue number3
DOIs
StatePublished - Jun 1 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Age Factors
  • Aged, 80 and over
  • Antibodies, Monoclonal, Humanized/therapeutic use
  • Antineoplastic Agents, Immunological/therapeutic use
  • Carcinoma, Transitional Cell/drug therapy
  • Cisplatin
  • Female
  • Humans
  • Male
  • Treatment Outcome
  • Urologic Neoplasms/drug therapy
  • Checkpoint inhibitor
  • Poor performance status
  • Bladder cancer
  • Cisplatin ineligible
  • Pembrolizumab
  • Programmed death 1
  • Immunotherapy
  • Aged
  • Urothelial carcinoma
  • Platinum ineligible

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