Idecabtagene vicleucel for relapsed/refractory multiple myeloma: a review of recent advances.

W. Tu, Ya-juan Xiao, Yadong Wang, R. Luo, Zhe S Chen
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引用次数: 1

Abstract

The introduction of new classes of drugs for the treatment of multiple myeloma (MM) in the past 2 decades, such as proteasome inhibitors, immunomodulators and anti-CD38 monoclonal antibodies, coupled with autologous stem cell transplantation, has approximately doubled the 5-year survival rate of MM patients. However, the patients eventually relapse and/or become resistant to the drugs and treatment. The recent emergence of anti-B-cell maturation antigen (BCMA) therapies, especially chimeric antigen receptor T-cell (CAR-T) immunotherapy targeting BCMA, holds great prospect in MM treatment. In this article, we review in detail the advances of idecabtagene vicleucel (ide-cel, bb-2121), the first CAR-T therapy targeting BCMA for treating relapse or refractory MM approved by the U.S. Food and Drug Administration (FDA) in 2021, including the preclinical study and phase I and II clinical trials. Also, it is predicted in this review that despite its amazing clinical efficacy and relatively lower toxicity, a lot of challenges and unsolved problems for ide-cel therapy remain in the way ahead.
Idecbtagene vicleucel治疗复发/难治性多发性骨髓瘤:最新进展综述。
在过去的20年里,用于治疗多发性骨髓瘤(MM)的新型药物的引入,如蛋白酶体抑制剂、免疫调节剂和抗CD38单克隆抗体,再加上自体干细胞移植,使MM患者的5年生存率大约翻了一番。然而,患者最终会复发和/或对药物和治疗产生耐药性。最近出现的抗B细胞成熟抗原(BCMA)疗法,特别是针对BCMA的嵌合抗原受体T细胞(CAR-T)免疫疗法,在MM治疗中具有很大的前景。在这篇文章中,我们详细回顾了idecabtagene vicleucel(ide cel,bb-2121)的进展,包括临床前研究和I期和II期临床试验,这是美国食品药品监督管理局(FDA)于2021年批准的第一种针对BCMA的CAR-T疗法,用于治疗复发或难治性MM。此外,这篇综述预测,尽管其具有惊人的临床疗效和相对较低的毒性,但ide-cel治疗仍有许多挑战和未解决的问题。
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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