Pembrolizumab in patients with CLL and Richter transformation or with relapsed CLL

被引:352
作者
Ding, Wei [1 ]
LaPlant, Betsy R. [2 ]
Call, Timothy G. [1 ]
Parikh, Sameer A. [1 ]
Leis, Jose F. [3 ]
He, Rong [4 ]
Shanafelt, Tait D. [1 ]
Sinha, Sutapa [1 ]
Le-Rademacher, Jennifer [2 ]
Feldman, Andrew L. [4 ]
Habermann, Thomas M. [1 ]
Witzig, Thomas E. [1 ]
Wiseman, Gregory A. [5 ]
Lin, Yi [1 ]
Asmus, Erik [2 ]
Nowakowski, Grzegorz S. [1 ]
Conte, Michael J. [1 ]
Bowen, Deborah A. [1 ]
Aitken, Casey N. [1 ]
Van Dyke, Daniel L. [6 ]
Greipp, Patricia T. [6 ]
Liu, Xin [7 ]
Wu, Xiaosheng [1 ]
Zhang, Henan [1 ]
Secreto, Charla R. [1 ]
Tian, Shulan [2 ]
Braggio, Esteban [3 ]
Wellik, Linda E. [1 ]
Micallef, Ivana [1 ]
Viswanatha, David S. [4 ]
Yan, Huihuang [2 ]
Chanan-Khan, Asher A. [8 ]
Kay, Neil E. [1 ]
Dong, Haidong [7 ]
Ansell, Stephen M. [1 ]
机构
[1] Mayo Clin, Div Hematol, 200 First St SW, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Hlth Sci Res, Rochester, MN USA
[3] Mayo Clin, Dept Hematol & Oncol, Scottsdale, AZ USA
[4] Mayo Clin, Div Hematopathol, Rochester, MN USA
[5] Mayo Clin, Dept Radiol, Rochester, MN USA
[6] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN USA
[7] Mayo Clin, Dept Immunol, Rochester, MN USA
[8] Mayo Clin, Div Hematol, Jacksonville, FL 32224 USA
基金
美国国家卫生研究院;
关键词
CHRONIC LYMPHOCYTIC-LEUKEMIA; HODGKIN-LYMPHOMA; PD-1; BLOCKADE; NIVOLUMAB; DYSFUNCTION; IPILIMUMAB; GUIDELINES; RITUXIMAB; IBRUTINIB; SAFETY;
D O I
10.1182/blood-2017-02-765685
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:3419 / 3427
页数:9
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