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https://hdl.handle.net/2445/173305
Title: | Pembrolizumab for Treatment-Refractory Metastatic Castration-Resistant Prostate Cancer: Multicohort, Open-Label Phase II KEYNOTE-199 Study |
Author: | Antonarakis, Emmanuel S. Piulats, Josep M. Gross-Goupil, Marine Goh, Jeffrey Ojamaa, Kristiina Hoimes, Christopher J. Vaishampayan, Ulka Berger, Raanan Sezer, Ahmet Alanko, Tuomo Wit, Ronald de Li, Chunde Omlin, Aurelius Procopio, Giuseppe Fukasawa, Satoshi Tabata, Ken-ichi Park, Se Hoon Feyerabend, Susan Drake, Charles G. Wu, Haiyan Qiu, Ping Kim, Jeri Poehlein, Christian Bono, Johann Sebastian de |
Keywords: | Càncer de pròstata Metàstasi Prostate cancer Metastasis |
Issue Date: | 10-Feb-2020 |
Publisher: | American Society of Clinical Oncology |
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. |
Note: | Reproducció del document publicat a: https://doi.org/10.1200/JCO.19.01638 |
It is part of: | Journal of Clinical Oncology, 2020, vol. 38, num. 5, p. 395-405 |
URI: | https://hdl.handle.net/2445/173305 |
Related resource: | https://doi.org/10.1200/JCO.19.01638 |
Appears in Collections: | Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) |
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AntonarakisES.pdf | 892.14 kB | Adobe PDF | View/Open |
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