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Update on the molecular pathogenesis and targeted approaches of mantle cell lymphoma: summary of the 12th annual conference of the European Mantle Cell Lymphoma Network

机译:外套细胞淋巴瘤的分子发病机理和靶向治疗方法的最新进展:欧洲外套细胞淋巴瘤网络第十二届年会摘要

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摘要

Mantle cell lymphoma (MCL) is a distinct subtype of malignant lymphoma which is characterized by the chromosomal translocation t(11;14)(q13;q32) resulting in constitutional overexpression of cyclin D1 and cell cycle dysregulation in almost all cases. Clinically, MCL shows an aggressive clinical course with a continuous relapse pattern and a median survival of only 3-5 years. However, recently a subset of 15% long-term survivors has been identified with a rather indolent clinical course. Targeted strategies include the proteasome inhibitors, immune modulatory drugs (IMiDs), mammalian target of rapamycin (mTOR) inhibitors and especially inhibitors of the B-cell receptor pathway. Our recent annual conference focused on the molecular pathogenesis of the disease and how these underlying molecular alterations may guide the selection and integration of innovative approaches for therapy. This review of the meeting covers in particular the identification of indolent cases, and deals with the role of the B-cell receptor pathway in MCL, as well as the detection of minimal residual disease and implementation of molecular approaches in current clinical trials.
机译:套细胞淋巴瘤(MCL)是恶性淋巴瘤的一种独特亚型,其特征是染色体易位t(11; 14)(q13; q32),导致几乎所有情况下细胞周期蛋白D1的结构性过度表达和细胞周期失调。在临床上,MCL表现出侵略性的临床过程,具有连续的复发模式,中位生存期仅为3-5年。但是,最近已经确定了一部分15%长期幸存者具有相当惰性的临床过程。靶向策略包括蛋白酶体抑制剂,免疫调节药物(IMiDs),雷帕霉素(mTOR)抑制剂的哺乳动物靶标,尤其是B细胞受体途径的抑制剂。我们最近的年度会议重点讨论了疾病的分子发病机理,以及这些潜在的分子变化如何指导创新疗法的选择和整合。会议的这次审查特别涵盖了惰性病例的鉴定,并探讨了M细胞中B细胞受体途径的作用,以及在当前的临床试验中检测到最小残留疾病和分子方法的实施。

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