Mantle Cell Lymphoma: Biological Insights and Treatment Advances

John P. Leonard , Michael E. Williams , Andre Goy , Steven Grant , Michael Pfreundschuh , Steve T. Rosen , John W. Sweetenham
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引用次数: 31

Abstract

Mantle cell lymphoma (MCL) exhibits considerable molecular heterogeneity and complexity, and is regarded as one of the most challenging lymphomas to treat. With increased understanding of the pathobiology of MCL, it is proposed that MCL is the result of 3 major converging factors, namely, deregulated cell cycle pathways, defects in DNA damage responses, and dysregulation of cell survival pathways. In the present era of targeted therapies, these biologic insights have resulted in the identification of several novel rational targets for therapeutic intervention in MCL that are undergoing active clinical testing. To date, there is no standard of care in MCL. Several approaches including conventional anthracycline-based therapies and intensive high-dose strategies with and without stem cell transplantation have failed to produce durable remissions for most patients. Moreover, considering the heterogeneity of MCL, it is increasingly being recognized that risk-adapted therapy might be a relevant therapeutic approach in this disease. At the first and second Global Workshops on Mantle Cell Lymphoma, questions addressing advances in the pathobiology of MCL, optimization of existing therapies, assessment of current data with novel therapeutic strategies, and the identification of molecular or phenotypic risk factors for utilization in risk-adapted therapies were discussed and will be summarized herein.

套细胞淋巴瘤:生物学见解和治疗进展
套细胞淋巴瘤(MCL)表现出相当大的分子异质性和复杂性,被认为是最具挑战性的淋巴瘤之一。随着对MCL病理生物学认识的增加,提出MCL是细胞周期通路失调、DNA损伤反应缺陷和细胞存活通路失调3个主要趋同因素的结果。在目前的靶向治疗时代,这些生物学见解已经导致了MCL治疗干预的几个新的合理靶点的确定,这些靶点正在进行积极的临床试验。到目前为止,MCL的治疗还没有标准。包括传统的蒽环类药物治疗和强化大剂量策略(包括或不包括干细胞移植)在内的几种方法未能对大多数患者产生持久的缓解。此外,考虑到MCL的异质性,人们越来越认识到风险适应疗法可能是该疾病的一种相关治疗方法。在第一届和第二届套细胞淋巴瘤全球研讨会上,讨论了MCL的病理生物学进展、现有治疗方法的优化、新治疗策略的现有数据评估以及风险适应疗法中分子或表型风险因素的识别等问题,并将在此进行总结。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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