| Literature DB >> 28424162 |
Wei Ding1, Betsy R LaPlant2, Timothy G Call1, Sameer A Parikh1, Jose F Leis3, Rong He4, Tait D Shanafelt1, Sutapa Sinha1, Jennifer Le-Rademacher2, Andrew L Feldman4, Thomas M Habermann1, Thomas E Witzig1, Gregory A Wiseman5, Yi Lin1, Erik Asmus2, Grzegorz S Nowakowski1, Michael J Conte1, Deborah A Bowen1, Casey N Aitken1, Daniel L Van Dyke6, Patricia T Greipp6, Xin Liu7, Xiaosheng Wu1, Henan Zhang1, Charla R Secreto1, Shulan Tian2, Esteban Braggio3, Linda E Wellik1, Ivana Micallef1, David S Viswanatha4, Huihuang Yan2, Asher A Chanan-Khan8, Neil E Kay1, Haidong Dong7, Stephen M Ansell1.
Abstract
Chronic lymphocytic leukemia (CLL) patients progressed early on ibrutinib often develop Richter transformation (RT) with a short survival of about 4 months. Preclinical studies suggest that programmed death 1 (PD-1) pathway is critical to inhibit immune surveillance in CLL. This phase 2 study was designed to test the efficacy and safety of pembrolizumab, a humanized PD-1-blocking antibody, at a dose of 200 mg every 3 weeks in relapsed and transformed CLL. Twenty-five patients including 16 relapsed CLL and 9 RT (all proven diffuse large cell lymphoma) patients were enrolled, and 60% received prior ibrutinib. Objective responses were observed in 4 out of 9 RT patients (44%) and in 0 out of 16 CLL patients (0%). All responses were observed in RT patients who had progression after prior therapy with ibrutinib. After a median follow-up time of 11 months, the median overall survival in the RT cohort was 10.7 months, but was not reached in RT patients who progressed after prior ibrutinib. Treatment-related grade 3 or above adverse events were reported in 15 (60%) patients and were manageable. Analyses of pretreatment tumor specimens from available patients revealed increased expression of PD-ligand 1 (PD-L1) and a trend of increased expression in PD-1 in the tumor microenvironment in patients who had confirmed responses. Overall, pembrolizumab exhibited selective efficacy in CLL patients with RT. The results of this study are the first to demonstrate the benefit of PD-1 blockade in CLL patients with RT, and could change the landscape of therapy for RT patients if further validated. This trial was registered at www.clinicaltrials.gov as #NCT02332980.Entities:
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Year: 2017 PMID: 28424162 PMCID: PMC5492091 DOI: 10.1182/blood-2017-02-765685
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113