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Updated: Jun 8, 2025

Tumor Engraftment in a Xenograft Mouse Model of Human Mantle Cell Lymphoma
Published on: March 30, 2018
Advances in the treatment of mantle cell lymphoma with BTK inhibitors
Jiwei Shen1, Jiawei Li2, Rui Yang2
1College of Pharmacy of Liaoning University, Shenyang, Liaoning 110036, PR China; API Engineering Technology Research Center of Liaoning Province, Shenyang, Liaoning 110036, PR China; Small molecular targeted drug R&D Engineering Research Center of Liaoning Province, Shenyang, Liaoning 110036, PR China.
Abstract:
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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