Pembrolizumab for Treatment-Refractory Metastatic Castration-Resistant Prostate Cancer: Multicohort, Open-Label Phase II KEYNOTE-199 Study

Author:

Antonarakis Emmanuel S.1,Piulats Josep M.2,Gross-Goupil Marine3,Goh Jeffrey45,Ojamaa Kristiina6,Hoimes Christopher J.7,Vaishampayan Ulka8,Berger Ranaan9,Sezer Ahmet10,Alanko Tuomo11,de Wit Ronald12,Li Chunde13,Omlin Aurelius14,Procopio Giuseppe15,Fukasawa Satoshi16,Tabata Ken-ichi17,Park Se Hoon18,Feyerabend Susan19,Drake Charles G.20,Wu Haiyan21,Qiu Ping22,Kim Jeri22,Poehlein Christian22,de Bono Johann Sebastian23

Affiliation:

1. Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD

2. Catalan Cancer Institute, Bellvitge Biomedical Research Institute, Centro de Investigación Biomédica en Red de Cáncer, Hospitalet de Llobregat, Barcelona, Spain

3. Institut Bergonié, Bordeaux, France

4. Royal Brisbane and Women’s Hospital, Herston, QLD, Australia

5. University of Queensland, St Lucia, QLD, Australia

6. East Tallinn Central Hospital, Tallinn, Estonia

7. Case Comprehensive Cancer Center at University Hospitals Seidman Cancer Center, Cleveland, OH

8. Karmanos Cancer Institute, Wayne State University, Detroit, MI

9. Chaim Sheba Medical Center, Tel Hashomer, Israel

10. Başkent University Hospital Adana, Adana, Turkey

11. Docrates Cancer Center, Helsinki, Finland

12. Erasmus MC Cancer Institute, Rotterdam, the Netherlands

13. Karolinska Institutet, Stockholm, Sweden

14. Cantonal Hospital St Gallen, University of Bern, Bern, Switzerland

15. Fondazione Istituto Nazionale Tumori, Milan, Italy

16. Chiba Cancer Center, Chiba, Japan

17. Kitasato University, Kanagawa, Japan

18. Sungkyunkwan University, Samsung Medical Center, Seoul, South Korea

19. Studienpraxis Urologie, Nürtingen, Germany

20. New York Presbyterian/Columbia University Medical Center, New York, NY

21. MSD China, Beijing, China

22. Merck & Co, Kenilworth, NJ

23. The Institute of Cancer Research and Royal Marsden Hospital, London, United Kingdom

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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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