Teclistamab-cqyv:首个用于治疗复发或难治性多发性骨髓瘤的双特异性t细胞结合抗体

Gwen Hua, Ryan Scanlan, Rachael Straining, Daniel S Carlson
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引用次数: 2

摘要

多发性骨髓瘤(MM)仍然是一种无法治愈的恶性肿瘤起源于浆细胞。尽管在治疗方面取得了重大进展,但复发仍然是不可避免的,因此仍然需要新的治疗方法。Teclistamab-cqyv是治疗MM的一类双特异性T细胞接合(BiTE)抗体。Teclistamab-cqyv通过结合T细胞表面表达的CD3受体和MM细胞和一些健康b系细胞表面表达的b细胞成熟抗原(BCMA)来激活免疫系统。在一项关键试验中,Teclistamab-cqyv已被证明是有效的,在重度预处理患者中显示出超过60%的总缓解率。与其他bcma靶向药物相比,teclistamab-cqyv的副作用特征表明老年患者更耐受。Teclistamab-cqyv现已被美国食品和药物管理局(FDA)批准作为治疗复发或难治性MM成人患者的单一疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Teclistamab-cqyv: The First Bispecific T-Cell Engager Antibody for the Treatment of Patients With Relapsed or Refractory Multiple Myeloma.

Multiple myeloma (MM) remains an incurable malignancy originating from plasma cells. Despite significant advances in treatment, relapses remain inevitable, and novel therapies continue to be needed. Teclistamab-cqyv is a first-in-class, bispecific T-cell engager (BiTE) antibody for the treatment of MM. Teclistamab-cqyv activates the immune system by binding to the cluster of differentiation 3 (CD3) receptor expressed on the surface of T cells and to the B-cell maturation antigen (BCMA) expressed on the surface of MM cells and some healthy B-lineage cells. Teclistamab-cqyv has been shown to be effective in a pivotal trial that demonstrated an overall response rate of more than 60% in heavily pretreated patients. Compared with other BCMA-targeted agents, the side effect profile of teclistamab-cqyv suggests a more tolerable option for elderly patients. Teclistamab-cqyv is now approved by the US Food and Drug Administration (FDA) as monotherapy for the treatment of adult patients with relapsed or refractory MM.

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