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原发性中枢神经系统淋巴瘤:分子发病机制与治疗进展

英文原题:Primary CNS lymphoma: update on molecular pathogenesis and therapy.

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Primary CNS lymphoma: update on molecular pathogenesis and therapy.

PubMed 2022/10/26(内容时间) Leuk Lymphoma Q3 · IF 2.1(JCR 2025)

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研究概要

原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见且侵袭性的结外非霍奇金淋巴瘤,作为脑肿瘤在诊断和管理方面带来了一系列独特的挑战。

中文摘要

原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见且侵袭性强的非霍奇金淋巴瘤结外亚型;作为脑肿瘤,它在诊断和管理方面面临独特挑战。随着新一代测序技术出现,本文综述对其分子和基因组发病机制的新认识,并重点介绍管理中的关键问题,关注新兴技术和新型生物疗法,包括单克隆抗体、免疫调节药物(IMiD)、布鲁顿酪氨酸激酶(BTK)抑制剂、PD-1抑制剂和CAR-T 治疗。整合应用这些方法可能增强诱导和巩固治疗效果,抑制NF-κB活化及抗肿瘤免疫应答,同时尽量减少基因毒性治疗常见的有害作用。

展开英文摘要原文

Primary central nervous system lymphoma (PCNSL) is a rare and aggressive form of extra-nodal non-Hodgkin lymphoma that as a brain tumor poses a unique set of challenges in diagnosis and management. With the advent of next-generation sequencing, we review updates in the understanding of its molecular and genomic pathogenesis. We also highlight key issues in management, with a focus on emerging technologies and new biological therapies including monoclonal antibodies, IMiDs, BTK inhibitors, PD-1 inhibitors, and CAR-T therapy. Integration of these approaches will likely enhance induction and consolidation strategies to suppress NF- B activation and the anti-tumor immune response, while minimizing the often noxious effects of genotoxic approaches.

论文信息

作者
Mo SS、Cleveland J、Rubenstein JL
单位
Department of Medicine, University of California, San Francisco, CA, USA.United States
文献类型
综述 · 美国 NIH 资助研究
期刊
Leukemia & lymphoma2023 Jan
原文标识
PubMed 36286546 · DOI 10.1080/10428194.2022.2133541