The shifting therapeutic paradigm for relapsed/refractory mantle cell lymphoma

被引:5
|
作者
Kumar, Sumukh Arun [1 ]
Gao, Jenny [2 ]
Patel, Shyam A. [3 ,4 ]
机构
[1] St Vincent Hosp, Dept Internal Med, Worcester, MA 01608 USA
[2] UMass Chan Med Sch, RNA Therapeut Inst, Worcester, MA USA
[3] UMass Chan Med Sch, Ctr Clin & Translat Sci CCTS, Worcester, MA 01655 USA
[4] UMass Chan Med Sch, UMass Mem Med Ctr, Dept Med, Div Hematol Oncol, 55 Lake Ave North, Worcester, MA 01655 USA
关键词
Mantle cell lymphoma; Targeted therapies; CAR-T; BTK inhibitor; Bispecific antibodies; TYROSINE KINASE INHIBITOR; CHRONIC LYMPHOCYTIC-LEUKEMIA; TARGETING BTK; PHASE; 1/2; IBRUTINIB; PIRTOBRUTINIB; ACALABRUTINIB; OUTCOMES;
D O I
10.1016/j.leukres.2023.107385
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mantle cell lymphoma (MCL) is a heterogeneous subtype of non-Hodgkin lymphoma that has been historically associated with poor 5-year overall survival rates, especially for aggressive variants. Traditional cytotoxic chemotherapy had been a mainstay of therapy for relapsed/refractory (R/R) MCL for many years until the advent of molecularly targeted therapies and cell-based approaches. However, a significant concern is the lack of definitive consensus guidelines for management of R/R MCL. The managerial conundrum partly stems from the absence of head-to-head comparisons of novel therapies, with conclusions drawn from cross-trial comparisons. In this evidence-based review, we discuss the current therapeutic options for R/R MCL, including the most recent data from the BRUIN study that led to the approval of the first-in-class non-covalent reversible Bruton's tyrosine kinase (BTK) inhibitor pirtobrutinib in 2023, as well as the recent removal of ibrutinib from the market. We discuss outlooks for targeted therapy and tolerability considerations for novel agents, including unique considerations for the elderly population. We highlight emerging data that support the curative potential of chimeric antigen receptor-T (CAR-T) therapy from ZUMA-2, relative to other promising investigational agents in the pipeline, including glofitamab, epcoritamab, and zilovertamab vedotin. We summarize management recommendations based upon the most rigorous clinical evidence to date.
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页数:6
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