"The End of the Golden Weather": therapeutic strategies for mantle cell lymphoma relapsed or refractory to covalent BTK inhibitors.

IF 8.2 1区 医学 Q1 HEMATOLOGY
Brian T Grainger, Chan Y Cheah
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引用次数: 0

Abstract

Mantle cell lymphoma (MCL) is a subtype of non-Hodgkin lymphoma which is often characterised by a pattern of continued relapse after frontline chemoimmunotherapy. Although patients are usually able to regain durable disease control with covalent Bruton's tyrosine kinase inhibitors (cBTKi) at first relapse, it is now appreciated that such responses are often not sustained and the management of such patients represents a significant area of unmet need. There is an imperative to better understand resistance mechanisms and identify high-risk subsets of patients for whom cBTKi responses may be particularly short. Allogeneic stem cell transplant has an established role in appropriate candidates, however contemporary consensus is to preferentially offer chimeric antigen receptor (CAR) T-cell therapy. In this Review, we consider the available data on both existing and emerging treatment options, including non-covalent BTK inhibitors, bispecific antibodies, antibody-drug conjugates and Bcl-2 inhibitors and propose a treatment strategy prioritising clinical trials where available.

"黄金天气的终结":共价 BTK 抑制剂复发或难治套细胞淋巴瘤的治疗策略。
套细胞淋巴瘤(MCL)是非霍奇金淋巴瘤的一种亚型,其特点通常是前线化疗免疫治疗后持续复发。虽然患者在首次复发时通常能够通过共价布鲁顿酪氨酸激酶抑制剂(cBTKi)重新获得持久的疾病控制,但现在人们意识到,这种反应往往不能持续,对这类患者的治疗是一个尚未满足需求的重要领域。当务之急是更好地了解耐药机制,并确定cBTKi反应可能特别短暂的高危患者亚群。同种异体干细胞移植对合适的候选者有既定的作用,但当代的共识是优先提供嵌合抗原受体(CAR)T细胞疗法。在本综述中,我们考虑了现有和新兴治疗方案的可用数据,包括非共价BTK抑制剂、双特异性抗体、抗体-药物共轭物和Bcl-2抑制剂,并提出了优先进行临床试验的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Haematologica
Haematologica 医学-血液学
CiteScore
14.10
自引率
2.00%
发文量
349
审稿时长
3-6 weeks
期刊介绍: Haematologica is a journal that publishes articles within the broad field of hematology. It reports on novel findings in basic, clinical, and translational research. Scope: The scope of the journal includes reporting novel research results that: Have a significant impact on understanding normal hematology or the development of hematological diseases. Are likely to bring important changes to the diagnosis or treatment of hematological diseases.
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