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PMID: 34044584 Published · ppublish English Journal Article

KEYNOTE-641: a Phase III study of pembrolizumab plus enzalutamide for metastatic castration-resistant prostate cancer.

Future oncology (London, England) ·Vol. 17 ·No. 23 ·2021-08-00 ·Pages 3017-3026

Graff JN, Liang LW, Kim J, Stenzl A

Abstract

Current treatment options for men with metastatic castration-resistant prostate cancer (mCRPC) are noncurative, and median survival upon development of mCRPC is approximately 3 years. The novel hormonal agent enzalutamide has an established role in the mCRPC treatment paradigm, and emerging evidence suggests potential synergism with enzalutamide and the PD-1 inhibitor pembrolizumab in men with mCRPC. Here, we describe the design and rationale for the multicenter, randomized, double-blind, Phase III KEYNOTE-641 study, which will be conducted to compare the efficacy and safety of pembrolizumab plus enzalutamide with that of enzalutamide plus placebo in mCRPC. Clinical trial registration: NCT03834493 (ClinicalTrials.gov).

Keywords
PD-1 PD-L1 castration resistant enzalutamide mCRPC pembrolizumab prostate cancer
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Graff Julie N ORCID
Portland VA Health Care System, 3710 SW US Veterans Hospital Road, P3HOC, Portland, OR 97239, USA. | Knight Cancer Institute, 3485 SW Bond Avenue, Portland, OR 97239, USA.
Liang Li Wen
MSD China, Building 21 Rongda Road, Chaoyang District, Beijing, China.
Kim Jeri
Merck & Co., Inc., 2000 Galloping Hill Road, Kenilworth, NJ 07033, USA.
Stenzl Arnulf
Hoppe-Seylerstrasse 3, University of Tuebingen Medical Center, Tuebingen, D-72076, Germany.
Article Info
Journal
Future oncology (London, England)
Abbr.
Future Oncol
ISSN
1744-8301
Published
2021-08-00
Epub
2021-00-28
Pages
3017-3026
Language
English
Region
England
NLM ID
101256629
Subset
IM
Grants
Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA
Databases
ClinicalTrials.gov
NCT03834493
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