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来那度胺、地塞米松联合伊沙佐米方案治疗达雷妥尤单抗暴露的复发/难治性多发性骨髓瘤患者的疗效:一项回顾性分析。

Efficacy of ixazomib, lenalidomide, dexamethasone regimen in daratumumab-exposed relapsed/refractory multiple myeloma patients: A retrospective analysis.

机构信息

Department of Internal Medicine, Hematology and Oncology, University Hospital Brno and Faculty of Medicine, Masaryk University, Brno, Czech Republic.

Central European Institute of Technology, Masaryk University, Brno, Czech Republic.

出版信息

Eur J Haematol. 2024 Dec;113(6):810-816. doi: 10.1111/ejh.14292. Epub 2024 Aug 26.

Abstract

We performed retrospective analysis of relapsed/refractory multiple myeloma (RRMM) patients previously exposed to daratumumab treated with ixazomib, lenalidomide, dexamethasone (IRd) regimen in real clinical practice. Our aim was to evaluate efficacy of IRd in these patients and select a subset of patients that would benefit from this treatment the most. In total, we analyzed 43 daratumumab-exposed RRMM patients treated in our center. Minimal response or better was achieved by 53.5% of patients from the cohort. Median progression free survival (PFS) was 4.56 months (95% CI: 2.56, 8.03) and median overall survival (OS) was 28.92 months (95% CI: 5.4, NR). Duration of response (DOR) was evaluable in 28 patients and reached a median of 21.3 months (95% CI: 6.85, NR). Next, we evaluated hazard ratios (HR) for OS and PFS. There was improved OS in patients that were not-triple refractory or worse (HR = 0.39, 95%Cl (0.14; 1.10), p = .07) and in patients, that had less than three previous lines of treatment (LOT) (HR = 0.13, 95%Cl (0.03; 0.6) p = .003). Similar to OS, there was improved PFS in patients, that were not triple-refractory or worse (HR = 0.52, 95%Cl (0.25; 1.10), p = .08). We concluded, that the best survival benefit for RRMM patients pretreated with daratumumab to IRd regimen was observed in patients that were not triple-refractory and had less than three previous lines of treatment (LOT). The DOR in these patients was 21.3 months (95% CI: 6.85, NR).

摘要

我们对先前接受过达雷妥尤单抗治疗的复发性/难治性多发性骨髓瘤(RRMM)患者进行了回顾性分析,这些患者在真实临床实践中接受了伊沙佐米、来那度胺和地塞米松(IRd)方案治疗。我们的目的是评估 IRd 在这些患者中的疗效,并选择最能从中受益的患者亚组。总共分析了我们中心治疗的 43 名达雷妥尤单抗暴露的 RRMM 患者。该队列中有 53.5%的患者达到了最小缓解或更好的缓解。中位无进展生存期(PFS)为 4.56 个月(95%CI:2.56,8.03),中位总生存期(OS)为 28.92 个月(95%CI:5.4,NR)。可评估 28 例患者的缓解持续时间(DOR),达到 21.3 个月的中位数(95%CI:6.85,NR)。接下来,我们评估了 OS 和 PFS 的危险比(HR)。无三重耐药或更差的患者 OS 改善(HR=0.39,95%Cl(0.14;1.10),p=0.07),且治疗线数(LOT)少于 3 线的患者 OS 改善(HR=0.13,95%Cl(0.03;0.6),p=0.003)。与 OS 相似,无三重耐药或更差的患者 PFS 改善(HR=0.52,95%Cl(0.25;1.10),p=0.08)。我们得出结论,在先前接受过达雷妥尤单抗治疗的 RRMM 患者中,接受 IRd 方案治疗的患者中,无三重耐药且 LOT 少于 3 线的患者的生存获益最佳。这些患者的 DOR 为 21.3 个月(95%CI:6.85,NR)。

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