Hua Gwen, Scanlan Ryan, Straining Rachael, Carlson Daniel S
Geisinger Enterprise Pharmacy, Danville, Pennsylvania.
Temple University, Philadelphia, Pennsylvania.
J Adv Pract Oncol. 2023 Mar;14(2):163-171. doi: 10.6004/jadpro.2023.14.2.7. Epub 2023 Mar 1.
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.
多发性骨髓瘤(MM)仍然是一种起源于浆细胞的无法治愈的恶性肿瘤。尽管在治疗方面取得了重大进展,但复发仍然不可避免,因此仍需要新的治疗方法。替雷利珠单抗-cqyv是一种一流的双特异性T细胞衔接器(BiTE)抗体,用于治疗MM。替雷利珠单抗-cqyv通过与T细胞表面表达的分化簇3(CD3)受体以及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)结合来激活免疫系统。在一项关键试验中,替雷利珠单抗-cqyv已被证明是有效的,该试验表明,在经过大量预处理的患者中,总体缓解率超过60%。与其他靶向BCMA的药物相比,替雷利珠单抗-cqyv的副作用表明它对老年患者来说是一个更可耐受的选择。替雷利珠单抗-cqyv现已被美国食品药品监督管理局(FDA)批准作为单一疗法,用于治疗复发或难治性MM的成年患者。