Emerging immunotherapies in the Hodgkin lymphoma armamentarium

被引:0
|
作者
Spinner, Michael A. [1 ]
Advani, Ranjana H. [2 ,3 ]
机构
[1] Univ Calif San Francisco, Dept Med, Div Hematol Oncol, San Francisco, CA USA
[2] Stanford Univ, Dept Med, Div Oncol, Stanford, CA USA
[3] Stanford Univ, Stanford Canc Inst, Dept Med, Div Oncol,Lymphoma, 875 Blake Wilbur Dr, Stanford, CA 94305 USA
关键词
Hodgkin lymphoma; immunotherapy; checkpoint inhibitor; antibody-drug conjugate; bispecific antibody; chimeric antigen receptor T-cell therapy; TUMOR-ASSOCIATED MACROPHAGES; OPEN-LABEL; T-CELLS; BRENTUXIMAB VEDOTIN; ANALYSIS REVEALS; PD-1; BLOCKADE; FOLLOW-UP; PHASE-II; MULTICENTER; EXPRESSION;
D O I
10.1080/14728214.2024.2349083
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionBrentuximab vedotin and PD-1 inhibitors have improved outcomes for classic Hodgkin lymphoma (cHL), but better therapies are needed for patients who relapse after these agents. Based on an improved understanding of cHL biology, there is a robust pipeline of novel therapies in development. In this review, we highlight emerging immunotherapeutic agents and combinations for cHL.Areas coveredWe review clinical trials of novel PD-1/PD-L1 inhibitors beyond FDA-approved agents, checkpoint inhibitors targeting CTLA-4, LAG-3, TIM-3, TIGIT, and CD47/SIRP alpha, PD-1 inhibitor combinations with immunomodulatory agents and epigenetic modifying therapies, antibody-drug conjugates, bispecific antibodies, and cellular therapies including anti-CD30 CAR-T and allogeneic NK cell therapy. We review the key safety and efficacy data from published phase 1-2 studies and highlight trials in progress, including the first phase 3 trial for PD-1 inhibitor-refractory cHL.Expert opinionMany novel immunotherapies hold great promise in cHL. Rational combinations with existing agents and next-generation antibody and CAR-T constructs may improve response rates and durability. Identifying biomarkers of response to these immunotherapies and using more sensitive tools to assess response, such as circulating tumor DNA, may further inform treatment decisions and enable a precision medicine approach in the future.
引用
收藏
页码:263 / 275
页数:13
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