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Pembrolizumab for treatment-refractory metastatic castration-resistant prostate cancer: Multicohort, open-label phase II KEYNOTE-199 study

  • Emmanuel S. Antonarakis
  • , Josep M. Piulats
  • , Marine Gross-Goupil
  • , Jeffrey Goh
  • , Kristiina Ojamaa
  • , Christopher J. Hoimes
  • , Ulka Vaishampayan
  • , Ranaan Berger
  • , Ahmet Sezer
  • , Tuomo Alanko
  • , Ronald de Wit
  • , Chunde Li
  • , Aurelius Omlin
  • , Giuseppe Procopio
  • , Satoshi Fukasawa
  • , Ken ichi Tabata
  • , Se Hoon Park
  • , Susan Feyerabend
  • , Charles G. Drake
  • , Haiyan Wu
  • Ping Qiu, Jeri Kim, Christian Poehlein, Johann Sebastian de Bono
  • Johns Hopkins University
  • University of Barcelona
  • Centre Georges-François Leclerc
  • Royal Brisbane and Women's Hospital
  • University of Queensland
  • East Tallinn Central Hospital
  • Case Western Reserve University
  • Wayne State University
  • Sheba Medical Center at Tel Hashomer
  • Baskent University
  • Docrates Cancer Center
  • Erasmus University Rotterdam
  • Karolinska Institutet
  • University of Bern
  • IRCCS Fondazione Istituto Nazionale per lo studio e la cura dei tumori - Milano
  • Chiba Cancer Center
  • Kitasato University
  • Studienpraxis Urologie
  • New York Presbyterian Hospital
  • MSD China
  • Merck
  • Institute of Cancer Research

Research output: Contribution to journalArticlepeer-review

Abstract

PURPOSE Pembrolizumab has previously shown antitumor activity against programmed death ligand 1 (PD-L1)–positive metastatic castration-resistant prostate cancer (mCRPC). Here, we assessed the antitumor activity and safety of pembrolizumab in three parallel cohorts of a larger mCRPC population. METHODS The phase II KEYNOTE-199 study included three cohorts of patients with mCRPC treated with docetaxel and one or more targeted endocrine therapies. Cohorts 1 and 2 enrolled patients with RECIST-measurable PD-L1–positive and PD-L1–negative disease, respectively. Cohort 3 enrolled patients with bone-predominant disease, regardless of PD-L1 expression. All patients received pembrolizumab 200 mg every 3 weeks for up to 35 cycles. The primary end point was objective response rate per RECIST v1.1 assessed by central review in cohorts 1 and 2. Secondary end points included disease control rate, duration of response, overall survival (OS), and safety. RESULTS Two hundred fifty-eight patients were enrolled: 133 in cohort 1, 66 in cohort 2, and 59 in cohort 3. Objective response rate was 5% (95% CI, 2% to 11%) in cohort 1 and 3% (95% CI,, 1% to 11%) in cohort 2. Median duration of response was not reached (range, 1.9 to $ 21.8 months) and 10.6 months (range, 4.4 to 16.8 months), respectively. Disease control rate was 10% in cohort 1, 9% in cohort 2, and 22% in cohort 3. Median OS was 9.5 months in cohort 1, 7.9 months in cohort 2, and 14.1 months in cohort 3. Treatment-related adverse events occurred in 60% of patients, were of grade 3 to 5 severity in 15%, and led to discontinuation of treatment in 5%. CONCLUSION Pembrolizumab monotherapy shows antitumor activity with an acceptable safety profile in a subset of patients with RECIST-measurable and bone-predominant mCRPC previously treated with docetaxel and targeted endocrine therapy. Observed responses seem to be durable, and OS estimates are encouraging.

Original languageEnglish
Pages (from-to)395-405
Number of pages11
JournalJournal of Clinical Oncology
Volume38
Issue number5
DOIs
StatePublished - 10 Feb 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

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