Department of Hematology, National Hospital Organization, Okayama Medical Center, Okayama, Japan.
Myeloma/Amyloidosis Center, Japanese Red Cross Medical Center, Tokyo, Japan.
Cancer Sci. 2020 Dec;111(12):4526-4539. doi: 10.1111/cas.14657. Epub 2020 Oct 15.
Isatuximab, an anti-CD38 monoclonal antibody, targets cells that strongly express CD38 including malignant plasma cells. This open-label, single-arm, multicenter, phase 1/2 trial investigated the tolerability/safety and efficacy of isatuximab monotherapy in Japanese patients with heavily pretreated, relapsed/refractory multiple myeloma (RRMM). In Phase 1, patients were sequentially assigned to receive isatuximab once weekly (QW) in cycle 1 (4 weeks) and every 2 weeks (Q2W) in subsequent cycles. Cohort 1 (n = 3) received 10 mg/kg QW/Q2W; cohort 2 (n = 5) received 20 mg/kg QW/Q2W. No dose-limiting toxicities occurred; the recommended dose for the single-arm phase 2 study (n = 28) was 20 mg/kg QW/Q2W. The overall safety profile was consistent with the current knowledge of isatuximab. The most common adverse events were infusion reactions (42.9%; 12/28); all were grade 1/2 and generally occurred during the first infusion. The overall response rate with 20 mg/kg QW/Q2W isatuximab was 36.4% (12/33); patients with high-risk cytogenetic abnormalities had comparable results. In phase 2, the median progression-free survival was 4.7 (95% confidence interval, 3.75 to not reached) months. Median overall survival was not reached. Isatuximab monotherapy was well tolerated and effective in patients with heavily pretreated RRMM including high-risk cytogenetic patients. This trial is registered at ClinicalTrials.gov as NCT02812706.
依沙妥昔单抗是一种抗 CD38 单克隆抗体,靶向表达 CD38 的细胞,包括恶性浆细胞。这项开放标签、单臂、多中心、1/2 期研究调查了伊沙妥昔单抗单药治疗日本复发/难治性多发性骨髓瘤(RRMM)患者的耐受性/安全性和疗效。在 1 期,患者依次接受伊沙妥昔单抗每周一次(QW)在第 1 周期(4 周)和随后每个周期每 2 周(Q2W)。队列 1(n=3)接受 10mg/kg QW/Q2W;队列 2(n=5)接受 20mg/kg QW/Q2W。未发生剂量限制毒性;单臂 2 期研究(n=28)的推荐剂量为 20mg/kg QW/Q2W。总体安全性与当前对伊沙妥昔单抗的了解一致。最常见的不良事件是输注反应(42.9%;28/28);均为 1/2 级,通常发生在第一次输注期间。20mg/kg QW/Q2W 伊沙妥昔单抗的总缓解率为 36.4%(28/33);具有高危细胞遗传学异常的患者具有可比的结果。在 2 期,中位无进展生存期为 4.7 个月(95%置信区间,3.75 至未达到)。中位总生存期未达到。伊沙妥昔单抗单药治疗在包括高危细胞遗传学患者在内的复发/难治性多发性骨髓瘤患者中具有良好的耐受性和疗效。该试验在 ClinicalTrials.gov 上注册为 NCT02812706。