Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
The Judy and Bernard Briskin Center for Multiple Myeloma Research, City of Hope, Duarte, California, USA.
Drugs Today (Barc). 2021 Nov;57(11):665-675. doi: 10.1358/dot.2021.57.11.3343690.
Isatuximab is an IgG1 monoclonal antibody targeting CD38 that has received regulatory approval in combination regimens for patients with relapsed/refractory multiple myeloma. CD38 is an antigen with high surface expression on multiple myeloma cells. While daratumumab holds most of the market share for this drug class, isatuximab offers several unique aspects including a mechanism of action that may involve more direct myeloma-cell inhibition and killing and less reliance on cross-linking and immune effector cells, as well as subgroup data from pivotal trials showing notable efficacy in populations with renal impairment, high-risk cytogenetics and the elderly. While the administration of the drug remains intravenous, studies of fixed-volume infusion and rapid infusion may improve drug administration convenience. Ongoing studies are examining isatuximab in combination with other immune therapies and cellular therapies, conventional chemotherapy and across other disease entities.
依沙替康是一种针对 CD38 的 IgG1 单克隆抗体,已在复发/难治性多发性骨髓瘤的联合治疗方案中获得监管批准。CD38 是一种在多发性骨髓瘤细胞上高表达的抗原。虽然达雷妥尤单抗在该药物类别中占据了大部分市场份额,但依沙替康具有几个独特的方面,包括作用机制可能涉及更直接的骨髓瘤细胞抑制和杀伤,较少依赖交联和免疫效应细胞,以及关键性试验的亚组数据显示在肾功能损害、高危细胞遗传学和老年人等人群中具有显著疗效。虽然该药物仍需静脉注射,但固定容量输注和快速输注的研究可能会提高药物给药的便利性。正在进行的研究正在评估依沙替康与其他免疫疗法和细胞疗法、常规化疗以及其他疾病实体的联合应用。