First clinical experience of isatuximab safety and tolerability in relapsed and refractory multiple myeloma: real-world data from a compassionate use program in Germany

T. Leitner, Cyrus Khandanpour, K. Wendelin, F. Oduncu, Christoph Kimmich, Ralph Naumann, Miriam Kull, Hartmut Goldschmidt, Martin Ehmer, C. Kiewitz, Hans-Jürgen Salwender
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Abstract

Therapy for relapsed and refractory multiple myeloma (RRMM) remains challenging. While monoclonal antibodies against CD38 combined with pomalidomide have demonstrated efficacy in clinical trials, real-world data remain sparse. We present real-world data from a compassionate use program (CUP) of isatuximab given in combination with pomalidomide and dexamethasone according to the German Compassionate Use Directive ahead of commercial availability for adult patients with RRMM. Patients had received at least two prior lines of therapy, including lenalidomide and a proteasome inhibitor (PI), and had demonstrated disease progression on the last therapy. Isatuximab was administered as part of the clinical routine. In total, 18 patients were included in the CUP before the official market availability of isatuximab. The data reflect a heterogeneous population in terms of age, risk factors, previous diseases, and treatments. Most of the patients had received two full isatuximab cycles. The analysis showed no new safety signals, supporting the manageable toxicity profile of isatuximab and highlighting its potential in real-world settings.
伊沙妥昔单抗对复发和难治性多发性骨髓瘤安全性和耐受性的首次临床经验:来自德国一项同情性使用计划的真实数据
复发性和难治性多发性骨髓瘤(RRMM)的治疗仍然充满挑战。虽然针对 CD38 的单克隆抗体联合泊马度胺在临床试验中显示出了疗效,但真实世界的数据仍然稀少。我们展示了一项同情使用计划(CUP)的真实数据,根据德国同情使用指令,伊沙妥昔单抗与泊马度胺和地塞米松联用,在RRMM成年患者中率先实现商业化。患者之前至少接受过两次治疗,包括来那度胺和蛋白酶体抑制剂(PI),并且在最后一次治疗中出现了疾病进展。伊沙妥昔单抗是临床常规治疗的一部分。在伊沙妥昔单抗正式上市之前,共有18名患者被纳入CUP。这些数据反映了人群在年龄、风险因素、既往疾病和治疗方面的异质性。大多数患者已经接受了两个完整的伊沙妥昔单抗周期。分析结果显示没有出现新的安全信号,支持了伊沙妥昔单抗可控的毒性特征,并突出了其在现实世界中的应用潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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