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复发/难治性 MCL 的治疗

英文原题:Treatment of relapsed/refractory MCL.

查看英文原题

Treatment of relapsed/refractory MCL.

PubMed 2025/02/13(内容时间) Blood Q1 · IF 23.9(JCR 2025)

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中文摘要

套细胞淋巴瘤(MCL)是一种罕见的B细胞非霍奇金淋巴瘤亚型,其临床特征为异质性行为,病程从惰性到高度侵袭性且预后有限不等。一线和复发 setting 中的靶向治疗选择正越来越多地塑造MCL的治疗格局。新的靶向和免疫治疗方法的开发与实施已改善了难治或复发性MCL患者的结局。然而,长期预后仍然有限,复发/难治性(R/R)疾病患者,尤其是那些BTK抑制剂治疗失败的患者,通常结局不佳。本综述总结了R/R MCL当前和新兴的治疗选择,重点关注联合靶向治疗策略的实施,如BTK抑制剂和BCL2抑制剂,以及免疫治疗方法,包括CAR-T 细胞和双特异性抗体。

展开英文摘要原文

Mantle cell lymphoma (MCL) is a rare subtype of B-cell non-Hodgkin lymphoma that is clinically characterized by its heterogeneous behavior, with courses ranging from indolent to highly aggressive cases with limited prognosis. Targeted treatment alternatives in first-line and relapse settings are more and more shaping the therapeutic landscape of MCL. The development and implementation of new targeted and immunotherapeutic approaches have already improved outcomes for patients with MCL with refractory or relapsed disease.

However, long-term prognosis is still limited, and patients with relapsed/refractory (R/R) disease, especially those failing Bruton tyrosine kinase (BTK) inhibitor treatment, usually have a dismal outcome. This review summarizes the current and emerging treatment options for R/R MCL, focusing on the implementation of combined targeted treatment strategies such as BTK inhibitors and BCL2 inhibitors, as well as immune-therapeutic approaches including chimeric antigen receptor T cells and bispecific antibodies.

论文信息

作者
Silkenstedt E、Dreyling M
单位
Department of Medicine III, Ludwig Maximilian University Hospital, Munich, Germany.Germany
文献类型
综述
期刊
Blood2025 Feb 13
原文标识
PubMed 39059015 · DOI 10.1182/blood.2023022353