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DARATUMUMAB: MONOCLONAL ANTIBODY THERAPY TO TREAT MULTIPLE MYELOMA

机译:达拉妥单抗:单克隆抗体疗法治疗多发性骨髓瘤

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摘要

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.
机译:Daratumumab(Darzalex(TM))是靶向CD38的人类单克隆抗体(MAb);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作用(ADCP),二次交联时的细胞凋亡和通过A的免疫调节作用免疫抑制细胞减少。 Daratumumab作为单一药物并与来那度胺合用,在经过大量预处理,复发的患者中具有良好的毒性,并具有令人鼓舞的临床活性,在这些患者中,其他新型药物(如硼替佐米,沙利度胺和来那度胺)和干细胞移植均已失败。鉴于令人鼓舞的疗效和可接受的安全性,daratumumab已作为单一疗法以及与常规和新型抗MM药物联合使用,成为MM的一种新型治疗选择。这项审查将侧重于daratumumab在MM中的临床前药理学,药代动力学,安全性和临床发展。

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