Please use this identifier to cite or link to this item: http://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: http://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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