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硼替佐米为基础的治疗转换至 IRd 在新诊断多发性骨髓瘤中是一种有效的方法。

-class transition from bortezomib-based therapy to IRd is an effective approach in newly diagnosed multiple myeloma.

机构信息

Rocky Mountain Cancer Centers/US Oncology Research, Denver, CO 80218, USA.

Department of Medicine, Division of Blood & Marrow Transplantation, Moores Cancer Center, University of California San Diego, La Jolla, CA 92037, USA.

出版信息

Future Oncol. 2024 Jan;20(3):131-143. doi: 10.2217/fon-2023-0272. Epub 2023 Oct 9.

Abstract

To compare the effectiveness of -class transition to all-oral ixazomib-lenalidomide-dexamethasone (IRd) following parenteral bortezomib (V)-based induction versus continued V-based therapy in US oncology clinics. Non-transplant eligible patients with newly diagnosed multiple myeloma (MM) receiving transition to IRd (N = 100; US MM-6), or V-based therapy (N = 111; INSIGHT MM). Following inverse probability of treatment weighting, overall response rate was 73.2% with IRd versus 57.5% with V-based therapy (p < 0.0001). Median duration of treatment was 10.8 versus 5.3 months (p < 0.0001). Overall, 18/24% of patients discontinued IRd/V-based therapy due to adverse events. IRd after V-based induction was associated with significantly improved overall response rate and duration of treatment than continued V-based combination therapy. : US MM-6: NCT03173092; INSIGHT MM: NCT02761187 (ClinicalTrials.gov).

摘要

比较 - 类别的有效性

向所有口服 ixazomib-lenalidomide-地塞米松(IRd)过渡

与继续基于硼替佐米(V)的治疗相比,在美国肿瘤学诊所中的疗效

适合接受新诊断多发性骨髓瘤(MM)的患者进行治疗(N=100;美国 MM-6),或接受基于 V 的治疗(N=111;INSIGHT MM)。

在进行治疗的逆概率加权后,IRd 的总缓解率为 73.2%,而 V 为 57.5%基于治疗(p<0.0001)。治疗的中位持续时间分别为 10.8 和 5.3 个月(p<0.0001)。总体而言,由于不良事件,18/24%的患者停止了 IRd/V 基于治疗。

V 基于诱导后 IRd 与继续 V 联合治疗相比,总体缓解率和治疗持续时间明显提高。:美国 MM-6:NCT03173092;INSIGHT MM:NCT02761187(ClinicalTrials.gov)。

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