CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The shifting therapeutic paradigm for relapsed/refractory mantle cell lymphoma.
The shifting therapeutic paradigm for relapsed/refractory mantle cell lymphoma.
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套细胞淋巴瘤(MCL)是非霍奇金淋巴瘤的一种异质性亚型,过去一直与较差的 5 年总生存率相关,侵袭性亚型尤其如此。多年来,传统细胞毒性化疗一直是复发/难治性(R/R)MCL 的主要治疗方法,直至分子靶向治疗和细胞疗法出现。当前一个重要问题是,R/R MCL 管理缺乏明确共识指南。管理困境部分源于新疗法之间缺乏头对头比较,结论往往依赖不同试验之间的比较。本循证综述讨论 R/R MCL 当前治疗选择,包括 BRUIN 研究的最新数据;该研究促使首创的非共价可逆 Bruton 酪氨酸激酶(BTK)抑制剂 pirtobrutinib 于 2023 年获批,以及近期 ibrutinib 撤出市场的情况。文章讨论靶向治疗前景和新型药物的耐受性考量,包括老年人群的特殊问题。
我们还重点介绍来自 ZUMA-2 的新兴数据,这些数据支持CAR-T(CAR-T)细胞疗法具有治愈潜力,并将其与研发管线中其他有前景的研究性药物进行比较,包括 glofitamab、epcoritamab 和 zilovertamab vedotin。最后,本文依据迄今最严格的临床证据总结管理建议。
Mantle cell lymphoma (MCL) is a heterogeneous subtype of non-Hodgkin lymphoma that has been historically associated with poor 5-year overall survival rates, especially for aggressive variants. Traditional cytotoxic chemotherapy had been a mainstay of therapy for relapsed/refractory (R/R) MCL for many years until the advent of molecularly targeted therapies and cell-based approaches.
However, a significant concern is the lack of definitive consensus guidelines for management of R/R MCL. The managerial conundrum partly stems from the absence of head-to-head comparisons of novel therapies, with conclusions drawn from cross-trial comparisons.
In this evidence-based review, we discuss the current therapeutic options for R/R MCL, including the most recent data from the BRUIN study that led to the approval of the first-in-class non-covalent reversible Bruton's tyrosine kinase (BTK) inhibitor pirtobrutinib in 2023, as well as the recent removal of ibrutinib from the market.
We discuss outlooks for targeted therapy and tolerability considerations for novel agents, including unique considerations for the elderly population.
We highlight emerging data that support the curative potential of chimeric antigen receptor-T (CAR-T) therapy from ZUMA-2, relative to other promising investigational agents in the pipeline, including glofitamab, epcoritamab, and zilovertamab vedotin.
We summarize management recommendations based upon the most rigorous clinical evidence to date.
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