Evaluating pirtobrutinib for the treatment of relapsed or refractory mantle cell lymphoma

被引:0
作者
Wang, Jacqueline F. [1 ]
Wang, Yucai [2 ]
机构
[1] NYU Langone Hlth, Dept Med, New York, NY USA
[2] Mayo Clin, Div Hematol, Rochester, MN 55905 USA
关键词
Mantle cell lymphoma; relapsed and/or refractory; Bruton tyrosine kinase inhibitor; pirtobrutinib; chimeric antigen receptor T-cell therapy; PHASE; 1/2; BRUIN; FOLLOW-UP; RESISTANCE MECHANISMS; SUBGROUP ANALYSIS; BTK; IBRUTINIB; INHIBITORS; SAFETY; START;
D O I
10.1080/17474086.2024.2389993
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionMantle cell lymphoma (MCL) is an uncommon non-Hodgkin lymphoma that is generally considered incurable. Covalent BTK inhibitors (cBTKi) are the cornerstone of treatment for relapsed or refractory (R/R) MCL, but treatment options are limited and prognosis is poor after cBTKi failure. Pirtobrutinib is a non-covalent BTK inhibitor that has demonstrated excellent efficacy and safety and represents an important new treatment in the evolving treatment landscape of R/R MCL.Areas coveredThis review will provide an overview of the therapeutic landscape of R/R MCL, characteristics of pirtobrutinib, and efficacy and safety data of pirtobrutinib in R/R MCL from pivotal clinical trials. PubMed and major hematology conference proceedings were searched to identify relevant studies involving pirtobrutinib.Expert opinionFor patients with R/R MCL that has progressed after treatment with cBTKi, pirtobrutinib is an important and efficacious treatment that confers favorable outcomes. In the post-cBTKi setting, when chimeric antigen receptor (CAR) T-cell therapy is not available or feasible, pirtobrutinib is the preferred treatment for R/R MCL. How to sequence or combine pirtobrutinib with CAR T-cell therapy and other available or emerging therapies requires further investigation. Future studies should also explore the role of pirtobrutinib in earlier lines of therapy for MCL.
引用
收藏
页码:651 / 659
页数:9
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