Teclistamab-cqyv: The First Bispecific T-Cell Engager Antibody for the Treatment of Patients With Relapsed or Refractory Multiple Myeloma.

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

Abstract

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.

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
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。
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