贝兰他单-马福多汀在复发/难治性多发性骨髓瘤中的实际应用:系统回顾

Abdelrahman Nanah, Samer Al Hadidi
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引用次数: 1

摘要

Belantamab mafodotin是一种针对b细胞成熟抗原的抗体药物偶联物,已于2020年8月获得美国食品和药物管理局(fda)的加速批准,用于复发或难治性多发性骨髓瘤成年患者,这些患者先前接受过至少4种治疗,包括抗cd38单克隆抗体、蛋白酶体抑制剂和免疫调节药物。2022年11月,belantamab mafodotin在一项验证性试验失败后从美国市场撤出。在我们的综述中,我们对在现实环境中使用belantamab mafodotin的有效性和安全性进行了系统的综述。
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Real-World Use of Belantamab Mafodotin in Relapsed/Refractory Multiple Myeloma: A Systematic Review
Belantamab mafodotin is an antibody drug conjugate directed against B-cell maturation antigen and was approved by the Food and Drug Administration under accelerated approval for use in the US in August 2020 for adult patients with relapsed or refractory multiple myeloma who have received at least 4 prior therapies, including an anti-CD38 monoclonal antibody, a proteasome inhibitor, and an immunomodulatory drug. In November 2022 belantamab mafodotin was withdrawn from the US market after failure of a required confirmatory trial. In our review, we provide a systematic review on the use of belantamab mafodotin efficacy and safety in a real-world setting.
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