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美法仑、环磷酰胺和地塞米松(MCD)作为复发/难治性多发性骨髓瘤患者挽救治疗的疗效和安全性

Efficacy and Safety of Melphalan, Cyclophosphamide and Dexamethasone (MCD) as a Salvage Treatment for Patients with Relapsed/Refractory Multiple Myeloma.

作者信息

Lee Seung-Shin, Lee Je-Jung

机构信息

Department of Hematology-Oncology, Wonkwang University Hospital, Iksan, Korea.

Department of Hematology-Oncology, Chonnam National University Hwasun Hospital, Hwasun, Korea.

出版信息

Chonnam Med J. 2019 Jan;55(1):25-30. doi: 10.4068/cmj.2019.55.1.25. Epub 2019 Jan 25.

Abstract

This study investigated the efficacy and safety of melphalan, cyclophosphamide, and dexamethasone (MCD) as a salvage regimen for heavily treated relapsed or refractory multiple myeloma patients. We retrospectively analyzed a total of 27 patients who received the MCD regimen between April 2011 and November 2013. The MCD regimen consisted of oral melphalan 6.75 mg/m on days 1-4, once-weekly dose of oral cyclophosphamide 300 mg/m and dexamethasone 20 mg/m on days 1-4 and days 15-18. Each cycle was repeated every 28 days. The median age of the patients was 66 years and the MCD regimen was initiated at a median 37.7 months from diagnosis. Patients received a median of five regimens including autologous stem cell transplantation. The overall response rate was 25.9% (very good partial response 3.7%, partial response 22.2%) and 8 (29.6%) patients achieved a minor response. Median progression-free survival was 5.6 months (95% confidence interval [CI], 4.2-8.5) ; overall survival 11.7 months (95% CI, 5.4-16.6). Grade 3 or 4 neutropenia and thrombocytopenia were observed in 51.8% and 33.3%, respectively. Although the overall response rate is relatively low, the MCD regimen may have a role as a bridge to a novel regimen in heavily pretreated patients with MM.

摘要

本研究调查了美法仑、环磷酰胺和地塞米松(MCD)作为挽救方案用于接受过大量治疗的复发或难治性多发性骨髓瘤患者的疗效和安全性。我们回顾性分析了2011年4月至2013年11月期间共27例接受MCD方案治疗的患者。MCD方案包括第1 - 4天口服美法仑6.75 mg/m²,第1 - 4天和第15 - 18天每周一次口服环磷酰胺300 mg/m²以及地塞米松20 mg/m²。每个周期每28天重复一次。患者的中位年龄为66岁,MCD方案在诊断后中位37.7个月开始使用。患者接受的方案中位数为5种,包括自体干细胞移植。总缓解率为25.9%(非常好的部分缓解3.7%,部分缓解22.2%),8例(29.6%)患者达到轻微缓解。中位无进展生存期为5.6个月(95%置信区间[CI],4.2 - 8.5);总生存期为11.7个月(95%CI,5.4 - 16.6)。3/4级中性粒细胞减少和血小板减少分别见于51.8%和33.3%的患者。尽管总缓解率相对较低,但MCD方案可能在接受过大量预处理的MM患者中作为通向新方案的桥梁发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9af1/6351330/3d5729af7cd2/cmj-55-25-g001.jpg

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