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来那度胺治疗多发性骨髓瘤:随机对照试验的系统评价和荟萃分析。

Lenalidomide treatment for multiple myeloma: systematic review and meta-analysis of randomized controlled trials.

机构信息

Department of Geriatric Hematology, Chinese PLA General Hospital, Beijing, China.

出版信息

PLoS One. 2013 May 14;8(5):e64354. doi: 10.1371/journal.pone.0064354. Print 2013.

Abstract

BACKGROUND

In recent years, a number of randomized controlled trials (RCTs) have reported on lenalidomide as a treatment for multiple myeloma (MM). Herein, we report results of a meta-analysis of RCTs examining the efficacy and safety of lenalidomide for MM.

PATIENTS AND METHODS

Databases were searched using the terms "lenalidomide or revlimid AND multiple myeloma."RCTs evaluating initial or maintenance therapeutic outcomes were included. Main outcome measures were response rates, progression-free survival (PFS), overall survival, and adverse events.

RESULTS

Seven trials were included (N = 192-614 participants). Lenalidomide doses and treatment regimens differed between trials. Complete response (CR) and very good partial response (VGPR) risk ratios (RR) favored lenalidomide over placebo (CR = 2.54, 95% confidence interval [CI] = 1.29-5.02; VGPR = 2.82, 95% CI = 1.30-6.09). The PFS hazard ratio favored lenalidomide over placebo (0.37, 95% CI = 0.33-0.41). For adverse events, neutropenia, deep vein thrombosis (DVT), infection, and hematologic cancer RR favored placebo over lenalidomide (neutropenia: 4.74, 95% CI = 2.96-7.57; DVT: 2.52; 95% CI: 1.60-3.98; infection: 1.98; 95% CI: 1.50-2.62; hematologic cancer: 3.20; 95% CI: 1.28-7.98).

CONCLUSIONS

Lenalidomide is an effective treatment for MM; however, treatment-related adverse events must be considered and appropriate adjustments and/or prophylactic treatment should be initiated where possible.

摘要

背景

近年来,多项随机对照试验(RCT)报道了来那度胺治疗多发性骨髓瘤(MM)的疗效。本研究对评估来那度胺治疗 MM 的疗效和安全性的 RCT 进行了荟萃分析。

患者与方法

检索使用“lenalidomide 或 revlimid AND multiple myeloma”等术语的数据库。纳入评估初始或维持治疗结果的 RCT。主要观察指标为缓解率、无进展生存期(PFS)、总生存期和不良事件。

结果

共纳入 7 项试验(N = 192-614 例患者)。试验之间来那度胺剂量和治疗方案不同。完全缓解(CR)和非常好的部分缓解(VGPR)风险比(RR)提示来那度胺优于安慰剂(CR:RR = 2.54,95%置信区间 [CI] = 1.29-5.02;VGPR:RR = 2.82,95% CI = 1.30-6.09)。PFS 风险比也提示来那度胺优于安慰剂(0.37,95% CI = 0.33-0.41)。关于不良事件,中性粒细胞减少、深静脉血栓形成(DVT)、感染和血液系统癌症 RR 提示安慰剂优于来那度胺(中性粒细胞减少症:RR = 4.74,95% CI = 2.96-7.57;DVT:RR = 2.52;95% CI = 1.60-3.98;感染:RR = 1.98;95% CI = 1.50-2.62;血液系统癌症:RR = 3.20;95% CI = 1.28-7.98)。

结论

来那度胺是 MM 的有效治疗药物;但是,必须考虑与治疗相关的不良反应,并在可能的情况下进行适当的调整和/或预防治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/461e/3653900/3a851feeb7c8/pone.0064354.g001.jpg

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