Advances in the treatment of mantle cell lymphoma with BTK inhibitors

被引:0
作者
Shen, Jiwei [1 ,2 ,3 ]
Li, Jiawei [1 ]
Yang, Rui [1 ]
Wu, Shuang [1 ]
Mu, Zhimei [1 ]
Ding, Shi [1 ,2 ,3 ]
Zhang, Xinyu [1 ]
Duo, Meiying [1 ]
Chen, Ye [1 ,2 ,3 ]
Liu, Ju [1 ,2 ,3 ]
机构
[1] Liaoning Univ, Coll Pharm, Shenyang 110036, Liaoning, Peoples R China
[2] API Engn Technol Res Ctr Liaoning Prov, Shenyang 110036, Liaoning, Peoples R China
[3] Small Mol Targeted Drug R&D Engn Res Ctr Liaoning, Shenyang 110036, Liaoning, Peoples R China
关键词
Mantle cell lymphoma; BTK inhibitor; Overcome resistance; TYROSINE KINASE INHIBITOR; NF-KAPPA-B; IBRUTINIB RESISTANCE; SINGLE-ARM; EFFICACY; PIRTOBRUTINIB; ACALABRUTINIB; TEMSIROLIMUS; MULTICENTER; RESPONSES;
D O I
10.1016/j.leukres.2024.107615
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mantle cell lymphoma (MCL) is a heterogenous disease that is one of the most challenging blood cancers due to its poor prognosis, high risk of relapse and drug resistance. Recent researches have brought significant changes in MCL patients outcomes and new clinical. Bruton's Tyrosine Kinase (BTK), a key kinase in the B-cell antigen receptor (BCR) signaling pathway, is a clinical research hot spot and plays a major role in the survival and spread of malignant B cells. The first generation of BTK inhibitors, led by ibrutinib, have shown promising results in targeted treatment. Meanwhile, several inhibitors have entered clinical studies and demonstrated outstanding therapeutic activity in clinical trials for MCL, indicating a good prospect for development. Despite these encouraging findings, the duration of response is limited, and resistance to BTK inhibitors develops in a portion of individuals. This review summarizes the pathogenesis of MCL and targeted BTK inhibitors and provides an overview of the mutations that can lead to resistance to BTK inhibitors. The purpose of this article is to review the literature describing these selective therapies and provides perspectives for their further development.
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页数:11
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