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:Evaluating pirtobrutinib for the treatment of relapsed or refractory mantle cell lymphoma.
Evaluating pirtobrutinib for the treatment of relapsed or refractory mantle cell lymphoma.
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对于接受 cBTKi 治疗后进展的 R/R MCL 患者,pirtobrutinib 是一种重要且有效的治疗选择,可带来有利的结局。在 post-cBTKi 背景下,当 CAR-T 细胞治疗不可用或不可行时,pirtobrutinib 是 R/R MCL 的首选治疗。如何将 pirtobrutinib 与 CAR-T 细胞治疗及其他可用或新兴疗法进行序贯或联合,仍需进一步研究。未来研究还应探索 pirtobrutinib 在 MCL 更早期治疗线中的作用。
套细胞淋巴瘤(MCL)是一种不常见的非霍奇金淋巴瘤,通常被认为无法治愈。共价BTK抑制剂(cBTKi)是复发/难治性(R/R)MCL治疗的基石,但cBTKi治疗失败后治疗选择有限且预后较差。Pirtobrutinib是一种非共价BTK抑制剂,已展现出优异的疗效和安全性,代表了R/R MCL不断演变的治疗格局中一种重要的新治疗方法。涵盖领域:本综述将概述R/R MCL的治疗格局、pirtobrutinib的特征,以及来自关键临床试验的pirtobrutinib在R/R MCL中的疗效和安全性数据。检索了PubMed和主要血液学会议论文集,以确定涉及pirtobrutinib的相关研究。
INTRODUCTION: Mantle cell lymphoma (MCL) is an uncommon non-Hodgkin lymphoma that is generally considered incurable. Covalent BTK inhibitors (cBTKi) are the cornerstone of treatment for relapsed or refractory (R/R) MCL, but treatment options are limited and prognosis is poor after cBTKi failure. Pirtobrutinib is a non-covalent BTK inhibitor that has demonstrated excellent efficacy and safety and represents an important new treatment in the evolving treatment landscape of R/R MCL. AREAS COVERED: This review will provide an overview of the therapeutic landscape of R/R MCL, characteristics of pirtobrutinib, and efficacy and safety data of pirtobrutinib in R/R MCL from pivotal clinical trials.
PubMed and major hematology conference proceedings were searched to identify relevant studies involving pirtobrutinib. EXPERT OPINION: For patients with R/R MCL that has progressed after treatment with cBTKi, pirtobrutinib is an important and efficacious treatment that confers favorable outcomes.
In the post-cBTKi setting, when chimeric antigen receptor (CAR) T-cell therapy is not available or feasible, pirtobrutinib is the preferred treatment for R/R MCL. How to sequence or combine pirtobrutinib with CAR T-cell therapy and other available or emerging therapies requires further investigation. Future studies should also explore the role of pirtobrutinib in earlier lines of therapy for MCL.
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