Pembrolizumab Plus Docetaxel Versus Docetaxel for Previously Treated Metastatic Castration-Resistant Prostate Cancer: The Randomized, Double-Blind, Phase III KEYNOTE-921 Trial
Abstract
PURPOSE The standard of care for metastatic castration-resistant prostate cancer (mCRPC) after second-generation androgen receptor pathway inhibitor (ARPI) therapy is still docetaxel. The randomized, double-blind, phase III KEYNOTE-921 trial (Clinicaltrials.gov identifier: NCT03834506 ) evaluated the efficacy and safety of pembrolizumab or placebo plus docetaxel for previously treated mCRPC. METHODS Adults with mCRPC who progressed after androgen-deprivation therapy and one ARPI were randomly assigned 1:1 to pembrolizumab or placebo plus docetaxel with concomitant prednisone. Dual primary end points were radiographic progression-free survival (rPFS) by blinded independent central review per Prostate Cancer Working Group 3–modified RECIST 1.1 and overall survival (OS). Safety was a secondary end point. RESULTS Between May 30, 2019, and June 17, 2021, 515 participants were randomly assigned to pembrolizumab plus docetaxel and 515 to placebo plus docetaxel. Median time from random assignment to data cutoff date (June 20, 2022) at final analysis (FA) was 22.7 months (range, 12.1-36.7). At first interim analysis (data cutoff date: September 27, 2021), median rPFS was 8.6 months (95% CI, 8.3 to 10.2) with pembrolizumab plus docetaxel versus 8.3 months (95% CI, 8.2 to 8.5) with placebo plus docetaxel (hazard ratio [HR], 0.85 [95% CI, 0.71 to 1.01]; P = .03). At FA, median OS was 19.6 months (95% CI, 18.2 to 20.9) versus 19.0 months (95% CI, 17.9 to 20.9), respectively (HR, 0.92 [95% CI, 0.78 to 1.09]; P = .17). Grade ≥3 treatment-related adverse events occurred in 43.2% of participants who received pembrolizumab plus docetaxel and 36.6% of participants who received placebo plus docetaxel. Two and seven participants, respectively, died due to a treatment-related adverse event. Pneumonitis was the most common immune-mediated adverse event (7.0% v 3.1%). CONCLUSION The addition of pembrolizumab to docetaxel did not significantly improve efficacy outcomes for participants with previously treated mCRPC. The current standard of care remains unchanged.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (26)
Daniel P. Petrylak
Yale School of Medicine, New Haven, CT
Raffaele Ratta
Hopital Foch, Suresnes, France
Nobuaki Matsubara
National Cancer Center Hospital East, Chiba, Japan
Ernesto Korbenfeld
British Hospital of Buenos Aires, Central British Hospital, Buenos Aires
Rustem Gafanov
Russian Scientific Center of Roentgen Radiology, Moscow, Russian Federation
Loic Mourey
Institut Claudius Regaud, IUCT-Oncopole, Toulouse, France
Tilman Todenhöfer
Studienpraxis Urologie, Nürtingen, Germany
Howard Gurney
Macquarie University, Sydney, NSW, Australia
Gero Kramer
Andries M. Bergman
Netherlands Cancer Institute, Amsterdam, the Netherlands
Pawel Zalewski
Lakeridge Health, Oshawa, ON, Canada
Maria de Santis
Andrew J. Armstrong
Winald Gerritsen
Radboud University Medical Center, Nijmegen, the Netherlands
Russell Pachynski
Washington University School of Medicine, St Louis, MO
Seok Soo Byun
Margitta Retz
Department of Urology, Technical University of Munich, School of Medicine and Health, TUM University Hospital Munich, Munich, Germany
Eric Levesque
CHU de Québec-Université Laval-Hôtel-Dieu de Québec, Québec City, QC, Canada
Ray McDermott
Sergio Bracarda
Azienda Ospedaliera Santa Maria, Terni, Italy
Ray Manneh
Sociedad de Oncología y Hematología del Cesar, Valledupar, Colombia
Meital Levartovsky
Chaim Sheba Medical Center, Ramat Gan, Israel
Xin Tong Li
Merck & Co., Inc., Rahway, NJ
Charles Schloss
Merck & Co., Inc., Rahway, NJ
Christian H. Poehlein
Merck & Co, Inc, Rahway, NJ
Karim Fizazi
Centre Oscar Lambret, University of Paris-Saclay, Lille, France