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卡非佐米挽救治疗复发或难治性多发性骨髓瘤患者的疗效和安全性:一项多中心回顾性观察研究。

Efficacy and safety of salvage therapy using Carfilzomib for relapsed or refractory multiple myeloma patients: a multicentre retrospective observational study.

机构信息

Institute of Haematology, Rabin Medical Centre, Petah Tikva, Israel.

Sackler Faculty of Medicine, Tel-Aviv University, Ramat Aviv, Israel.

出版信息

Br J Haematol. 2016 Jan;172(1):89-96. doi: 10.1111/bjh.13799. Epub 2015 Nov 16.

DOI:10.1111/bjh.13799
PMID:26567759
Abstract

Carfilzomib has been established in previous years as a treatment for patients with relapsed and/or refractory multiple myeloma (RR-MM). A retrospective multicentre study to evaluate the clinical use of carfilzomib for RR-MM outside of a clinical trial setting was conducted by our group. One hundred and thirty-five patients were included. All patients had been previously exposed to bortezomib and 93% had also been treated with lenalidomide. The vast majority of patients received carfilzomib as part of a two- or three-drug combination. The overall response rate was 47·2%. Multivariate analysis revealed bortezomib resistance, lenalidomide resistance and albumin <35 g/l to negatively impact the likelihood of achieving response. The median duration of response was 8·4 months, and was significantly higher in patients receiving three-drug combination and patients presenting without extramedullary disease. The median progression-free survival and overall survival for the entire cohort was 4·9 months (95% confidence interval [CI] 3·8-6·4) and 12·2 months (95% CI 9-not reached), respectively. Toxicity was manageable, although treatment-related death was seen in 5% of patients. In the setting of progressive multiple myeloma, carfilzomib in a combination regimens yields effective results with a manageable toxicity.

摘要

卡非佐米在过去几年中已被确立为治疗复发和/或难治性多发性骨髓瘤(RR-MM)的方法。我们的团队进行了一项回顾性多中心研究,以评估卡非佐米在临床试验之外用于 RR-MM 的临床应用。共纳入了 135 例患者。所有患者均曾接受硼替佐米治疗,93%的患者还接受过来那度胺治疗。绝大多数患者接受了卡非佐米联合两种或三种药物的治疗。总体缓解率为 47.2%。多变量分析显示,硼替佐米耐药、来那度胺耐药和白蛋白<35g/l 与缓解率的降低显著相关。中位缓解持续时间为 8.4 个月,接受三联治疗和无髓外疾病的患者缓解持续时间显著更长。整个队列的中位无进展生存期和总生存期分别为 4.9 个月(95%置信区间 [CI] 3.8-6.4)和 12.2 个月(95% CI 9-未达到)。毒性是可管理的,尽管有 5%的患者出现了与治疗相关的死亡。在进展性多发性骨髓瘤中,卡非佐米联合治疗方案具有有效的疗效,毒性可管理。

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