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来那度胺和皮质类固醇联合按需环磷酰胺治疗复发/难治性多发性骨髓瘤患者的回顾性分析:一项单中心经验。

Addition of Cyclophosphamide "On Demand" to Lenalidomide and Corticosteroids in Patients With Relapsed/Refractory Multiple Myeloma-A Retrospective Review of a Single-center Experience.

机构信息

Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, ON, Canada.

Department of Biostatistics, Princess Margaret Cancer Centre, Toronto, ON, Canada.

出版信息

Clin Lymphoma Myeloma Leuk. 2019 Apr;19(4):e195-e203. doi: 10.1016/j.clml.2018.12.007. Epub 2018 Dec 20.

Abstract

INTRODUCTION

The combination of lenalidomide and dexamethasone (Len-Dex) is an established regimen for patients with relapsed or refractory myeloma. To prolong the benefit of this effective regimen, the Myeloma Program at Princess Margaret Cancer Centre has routinely added a third agent, oral cyclophosphamide (Cy) given weekly, to Len-Dex at disease progression.

PATIENTS AND METHODS

In the present report, we describe the cases of 53 patients who had received Len-Dex-Cy for a minimum of 4 weeks from January 2007 to December 2014 after progression with Len-Dex alone. The dose of added Cy ranged from 250 to 500 mg weekly. The median number of previous regimens, including Len-Dex, was 2 (range, 2-4); 80% of patients had undergone previous autologous stem cell transplantation.

RESULTS

The overall rate of response equal to or greater than a partial response was 34%, and clinical benefit (stable disease or better) was observed in 87% of the patients. The median duration of Len-Dex-Cy therapy was 6.9 months (range, 0.9-55.1 months). The median progression-free survival was 6.1 months (range, 4.2-8.1 months) from the addition of Cy and 24.1 months (range, 15.9-32.0 months) from start of Len-Dex.

CONCLUSION

The addition of Cy for patients with myeloma developing progression with Len-Dex was an inexpensive option with manageable toxicity that resulted in a clinically meaningful extension of disease control.

摘要

简介

来那度胺联合地塞米松(Len-Dex)是复发性或难治性骨髓瘤患者的既定治疗方案。为了延长这种有效方案的益处,玛格丽特公主癌症中心的骨髓瘤项目在疾病进展时常规将第三种药物,即每周给予的口服环磷酰胺(Cy),加入到 Len-Dex 中。

患者和方法

在本报告中,我们描述了 53 例患者的病例,这些患者在单独使用 Len-Dex 进展后,从 2007 年 1 月至 2014 年 12 月至少接受了 4 周的 Len-Dex-Cy 治疗。加入的 Cy 剂量范围为每周 250 至 500 毫克。包括 Len-Dex 在内的先前治疗方案的中位数为 2 个(范围,2-4);80%的患者接受过自体干细胞移植。

结果

总反应率等于或大于部分反应率为 34%,87%的患者观察到临床获益(稳定疾病或更好)。Len-Dex-Cy 治疗的中位持续时间为 6.9 个月(范围,0.9-55.1 个月)。从加入 Cy 开始,Len-Dex 的中位无进展生存期为 6.1 个月(范围,4.2-8.1 个月),从开始 Len-Dex 开始为 24.1 个月(范围,15.9-32.0 个月)。

结论

对于因使用 Len-Dex 而进展的骨髓瘤患者,加入 Cy 是一种廉价的选择,具有可管理的毒性,可显著延长疾病控制。

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