Department of Medicine, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Centre for Lymphoid Cancer, BC Cancer, Vancouver, BC, Canada.
Leuk Lymphoma. 2024 Aug;65(8):1044-1054. doi: 10.1080/10428194.2024.2338851. Epub 2024 Apr 18.
In this review we summarize the current evidence describing the management of patients with relapsed/refractory MCL and outline the various novel therapeutics that have been developed over the past two decades. We also describe how overall response rates, complete response rates, duration of responses, and life expectancy have dramatically increased with the introduction of novel therapies, particularly covalent Bruton Tyrosine Kinase inhibitors (BTKi) and chimeric antigen receptor T-cell (CAR-T) therapy. The most recent emerging options for patients with progressive disease following BTKi or CAR-T, including non-covalent BTKi, antibody-drug conjugates, Bcl-2 inhibitors, and bispecific antibodies, may further improve response rates and outcomes. Future directions should focus on identifying the best sequencing and/or combinations of the increasingly available treatment options while prioritizing strategies with curative potential.
在这篇综述中,我们总结了目前描述复发性/难治性 MCL 患者管理的证据,并概述了过去二十年开发的各种新型治疗方法。我们还描述了随着新型治疗方法,特别是共价 Bruton 酪氨酸激酶抑制剂(BTKi)和嵌合抗原受体 T 细胞(CAR-T)疗法的引入,总体缓解率、完全缓解率、反应持续时间和预期寿命是如何显著提高的。对于 BTKi 或 CAR-T 治疗后疾病进展的患者,最近出现的新选择,包括非共价 BTKi、抗体药物偶联物、Bcl-2 抑制剂和双特异性抗体,可能会进一步提高缓解率和改善预后。未来的方向应该集中在确定最佳的治疗方案排序和/或组合,同时优先考虑具有治愈潜力的策略。