Daratumumab:单克隆抗体治疗多发性骨髓瘤。

C. Xia, M. Ribeiro, S. Scott, S. Lonial
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引用次数: 3

摘要

Daratumumab (Darzalex[TM])是一种靶向CD38的人单克隆抗体(MAb);一种在多发性骨髓瘤(MM)细胞中高度表达的表面蛋白。临床前研究表明,daratumumab通过多种机制诱导MM细胞死亡,包括补体依赖性细胞毒性(CDC)、抗体依赖性细胞介导的细胞毒性(ADCC)、抗体依赖性细胞吞噬(ADCP)、继发性交联后的细胞凋亡以及通过减少免疫抑制细胞产生的免疫调节作用。Daratumumab具有良好的毒性特征和令人鼓舞的临床活性,可作为单药和与来那度胺联合使用,用于重度预处理的复发患者,这些患者的其他新药(如硼替佐米、沙利度胺和来那度胺)和干细胞移植已经失败。鉴于令人鼓舞的疗效和可接受的安全性,daratumumab已成为MM的一种新的治疗选择,既可以作为单一治疗,也可以与传统和新型抗MM药物联合使用。本文将重点讨论daratumumab治疗MM的临床前药理学、药代动力学、安全性和临床发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Daratumumab: monoclonal antibody therapy to treat multiple myeloma.
Daratumumab (Darzalex[TM]) is a human monoclonal antibody (MAb) that targets CD38; a surface protein highly expressed across multiple myeloma (MM) cells. Preclinical studies have shown daratumumab induces MM cell death through several mechanisms, including complement-dependent cytotoxicity (CDC) antibody-dependent cell-mediated cytotoxicity (ADCC), antibody-dependent cellular phagocytosis (ADCP), apoptosis upon secondary crosslinking and immunomodulatory effects via a decrease in immune suppressive cells. Daratumumab has a favorable toxicity profile and encouraging clinical activity as a single agent and in combination with lenalidomide in heavily pretreated, relapsed patients in whom other novel agents (such as bortezomib, thalidomide and lenalidomide) and stem cell transplant have already failed. Given the encouraging efficacy and acceptable safety profile, daratumumab has emerged as a novel treatment option for MM both as a monotherapy and in combination with conventional and novel anti-MM agents. This review will focus on preclinical pharmacology, pharmacokinetics, safety and clinical development of daratumumab in MM.
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