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Teclistamab 用于多发性骨髓瘤:首创双特异性抗体的临床见解与实践考量

英文原题:Teclistamab for Multiple Myeloma: Clinical Insights and Practical Considerations for a First-in-Class Bispecific Antibody.

查看英文原题

Teclistamab for Multiple Myeloma: Clinical Insights and Practical Considerations for a First-in-Class Bispecific Antibody.

PubMed 2023/07/21(内容时间) Cancer Manag Res Q3 · IF 2.6(JCR 2025)

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中文摘要

Teclistamab是一种BCMAxCD3双特异性抗体,是首个获批用于治疗复发/难治性多发性骨髓瘤的药物。鉴于其在经过大量预处理的患者中具有显著疗效,且相较于靶向BCMA的CAR-T 细胞更易获得,teclistamab必将成为复发/难治性多发性骨髓瘤治疗的基石。Teclistamab具有一系列值得注意的不良反应,包括细胞因子释放综合征(CRS)、感染和神经毒性,医务人员必须采取独特的预防措施和预防性干预。本文综述了促使teclistamab获批的临床前和临床数据、重要的患者选择考量、CRS及其他副作用的管理策略,以及双特异性抗体治疗多发性骨髓瘤的未来前景。

展开英文摘要原文

Teclistamab is a BCMAxCD3 bispecific antibody, the first approved for the treatment of relapsed or refractory multiple myeloma. Given its impressive efficacy in heavily pretreated patients and better accessibility compared to BCMA-directed CAR T cells, teclistamab is sure to become a staple of relapsed/refractory multiple myeloma therapy. Teclistamab carries a set of notable adverse effects including cytokine release syndrome (CRS), infections, and neurotoxicity for which providers must take unique precautions and prophylactic measures.

Here, we review the preclinical and clinical data, which led to teclistamab's approval, important patient selection considerations, strategies for managing CRS and other side effects, and finally the future of bispecific antibody therapy in multiple myeloma.

论文信息

作者
Pan D、Richter J
单位
Division of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.United States
文献类型
综述
期刊
Cancer management and research2023
原文标识
PubMed 37497430 · DOI 10.2147/CMAR.S372237