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来那度胺治疗急性髓系白血病的疗效与安全性:一项系统评价和荟萃分析

Efficacy and safety of lenalidomide for the treatment of acute myeloid leukemia: a systematic review and meta-analysis.

作者信息

Xie Chun-Hong, Wei Min, Yang Fei-Yan, Wu Fu-Zhen, Chen Lei, Wang Jian-Kun, Liu Qin, Huang Jin-Xiong

机构信息

Department of Hematology, Affiliated Liuzhou People's Hospital of Guangxi University of Science and Technology (Liuzhou People's Hospital), Liuzhou 545000, Guangxi, China,

出版信息

Cancer Manag Res. 2018 Sep 18;10:3637-3648. doi: 10.2147/CMAR.S168610. eCollection 2018.

Abstract

BACKGROUND

Lenalidomide is effective for the treatment of low-risk myelodysplastic syndromes with deletion 5q abnormalities. However, whether lenalidomide leads to a significant improvement in treatment response and overall survival (OS) in cases of acute myeloid leukemia (AML) remains controversial. A systematic review and a meta-analysis were performed to evaluate the efficacy and safety of lenalidomide in the treatment of AML.

METHODS

Clinical studies were identified from the Cochrane Central Register of Controlled Trials, PubMed, Embase, and ClinicalTrials.gov. Efficacy outcomes included overall response rate (ORR), complete remission (CR), and OS. Safety was evaluated based on the incidence of grade 3 and 4 treatment-related adverse events (AEs).

RESULTS

Eleven studies were included in our meta-analysis; collectively these studies featured 407 AML patients. Pooled estimates for overall ORR and CR were 31% (95% CI: 26%-36%) and 21% (95% CI: 16%-27%), respectively. Thrombocytopenia, anemia, neutropenia, and infection were the most common grade 3 and 4 AEs.

CONCLUSION

Lenalidomide may have some clinical activity in AML, but the population that would benefit from lenalidomide and incorporating lenalidomide into combination drug strategies need to be better defined.

摘要

背景

来那度胺对治疗伴有5q缺失异常的低危骨髓增生异常综合征有效。然而,来那度胺在急性髓系白血病(AML)患者中是否能显著改善治疗反应和总生存期(OS)仍存在争议。我们进行了一项系统评价和荟萃分析,以评估来那度胺治疗AML的疗效和安全性。

方法

从Cochrane对照试验中央注册库、PubMed、Embase和ClinicalTrials.gov中检索临床研究。疗效指标包括总缓解率(ORR)、完全缓解(CR)和OS。根据3级和4级治疗相关不良事件(AE)的发生率评估安全性。

结果

我们的荟萃分析纳入了11项研究,这些研究共涉及407例AML患者。汇总估计的总ORR和CR分别为31%(95%CI:26%-36%)和21%(95%CI:16%-27%)。血小板减少、贫血、中性粒细胞减少和感染是最常见的3级和4级AE。

结论

来那度胺在AML中可能具有一定的临床活性,但需要更好地明确能从该药中获益的人群以及将其纳入联合用药策略的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87ba/6152603/f72508725e26/cmar-10-3637Fig1.jpg

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