BTK Inhibitors and CAR T-Cell Therapy in Treating Mantle Cell Lymphoma-Finding a Dancing Partner

被引:15
|
作者
Munoz, Javier L. [1 ]
Wang, Yucai [2 ]
Jain, Preetesh [3 ]
Wang, Michael [3 ]
机构
[1] Mayo Clin, Phoenix, AZ USA
[2] Mayo Clin, Rochester, MN USA
[3] Univ Texas Houston, MD Anderson Canc Ctr, Dept Lymphoma Myeloma, Div Canc Med, 1515 Holcombe Blvd, Houston, TX 77030 USA
关键词
Bruton's tyrosine kinase; Chimeric antigen receptor T-cell therapy; Relapsed; refractory mantle cell lymphoma; Combination therapy; CHRONIC LYMPHOCYTIC-LEUKEMIA; WALDENSTROM MACROGLOBULINEMIA; IBRUTINIB; ZANUBRUTINIB; EFFICACY; FAILURE;
D O I
10.1007/s11912-022-01286-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of Review This review focuses on the feasibility of combining Bruton's tyrosine kinase (BTK) inhibitors (BTKis) with chimeric antigen receptor (CAR) T-cell therapy in patients with relapsed or refractory (R/R) mantle cell lymphoma (MCL). Potential scenarios for combination treatment with these agents are presented. Recent Findings BTKis and CAR T-cell therapy have revolutionized the treatment paradigm for R/R MCL. Ibrutinib, acalabrutinib, and zanubrutinib are covalent irreversible BTKis approved for R/R MCL. Brexucabtagene autoleucel was the first CAR T-cell therapy approved for R/R MCL based on findings from the ZUMA-2 trial. There is evidence to suggest that combination treatment with BTKis and CAR T-cell therapy may improve CAR T-cell efficacy. As BTKis and CAR T-cell therapy become mainstays in R/R MCL therapy, combination treatment strategies should be evaluated for their potential benefit in R/R MCL.
引用
收藏
页码:1299 / 1311
页数:13
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