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Advances in Molecular Biology and Targeted Therapy of Mantle Cell Lymphoma

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2019 Sep 11
PMID 31500350
Citations 12
Authors
Affiliations
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Abstract

Mantle cell lymphoma (MCL) is a heterogeneous malignancy with a broad spectrum of clinical behavior from indolent to highly aggressive cases. Despite the fact that MCL remains in most cases incurable by currently applied immunochemotherapy, our increasing knowledge on the biology of MCL in the last two decades has led to the design, testing, and approval of several innovative agents that dramatically changed the treatment landscape for MCL patients. Most importantly, the implementation of new drugs and novel treatment algorithms into clinical practice has successfully translated into improved outcomes of MCL patients not only in the clinical trials, but also in real life. This review focuses on recent advances in our understanding of the pathogenesis of MCL, and provides a brief survey of currently used treatment options with special focus on mode of action of selected innovative anti-lymphoma molecules. Finally, it outlines future perspectives of patient management with progressive shift from generally applied immunotherapy toward risk-stratified, patient-tailored protocols that would implement innovative agents and/or procedures with the ultimate goal to eradicate the lymphoma and cure the patient.

Citing Articles

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Expression of PD1 and PDL1 as immune-checkpoint inhibitors in mantle cell lymphoma.

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CircCTNNA1 is Upregulated in Mantle Cell Lymphoma and Predicts Poor Survival by Sponging miR-34a to Increase Cell Proliferation.

Lu C, Song C, Han Q, Jing X Mediterr J Hematol Infect Dis. 2022; 14(1):e2022047.

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Cost-Effectiveness of Brexucabtagene Autoleucel versus Best Supportive Care for the Treatment of Relapsed/Refractory Mantle Cell Lymphoma following Treatment with a Bruton's Tyrosine Kinase Inhibitor in Canada.

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Inhibition of LINK-A lncRNA overcomes ibrutinib resistance in mantle cell lymphoma by regulating Akt/Bcl2 pathway.

Zhang Y, Lu P, Zhou Y, Zhang L PeerJ. 2022; 9:e12571.

PMID: 35003920 PMC: 8686732. DOI: 10.7717/peerj.12571.


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