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贝利尤单抗联合标准治疗对系统性红斑狼疮患者的疗效与安全性:一项荟萃分析

Efficacy and Safety of Belimumab Plus Standard Therapy in Patients With Systemic Lupus Erythematosus: A Meta-analysis.

作者信息

Wei Li-Qiang, Liang Yong-Gang, Zhao Yong, Liang Hui-Tao, Qin Dong-Chun, She Ming-Cong

机构信息

Department of Clinical Laboratory, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.

Zhengzhou Central Hospital Affiliated with Zhengzhou University, Zhengzhou, Henan, China.

出版信息

Clin Ther. 2016 May;38(5):1134-40. doi: 10.1016/j.clinthera.2016.02.022. Epub 2016 Mar 25.

Abstract

PURPOSE

The treatment of belimumab plus standard therapy in patients with systemic lupus erythematosus (SLE) has been studied extensively in recent years. Our aim was to estimate the efficacy and safety of this therapy compared with placebo plus standard therapy in patients with SLE.

METHODS

PubMed, Web of Science, Embase, Chinese Biomedical Literature Database (CBM, Chinese), and Wanfang Database (Chinese) were searched for all randomized clinical trials that mainly studied the efficacy and safety of belimumab plus standard therapy before June 2015. We extracted or calculated the rate of the SLE Response Index and adverse event rate at 52 weeks in all the included studies. The odds ratio (OR) with 95% CI between the 2 groups in this meta-analysis was conducted by using a random-effects model. Sensitivity and publication bias analyses were also performed. All statistical tests were performed by using Stata software version 12.0 (StataCorp., College Station, Texas).

FINDINGS

In the overall samples (4 studies, N = 4692 ), a significantly higher SLE Response Index rate at 52 weeks was found in belimumab plus standard therapy group compared with the placebo plus standard therapy group in all studies (OR = 1.49; 95% CI, 1.26-1.77 ; P < 0.001 ). When assessed with the incidence of serious adverse events, the data revealed that there was no significant difference between the 2 groups, with pooled OR = 1.08; 95% CI, 0.83-1.39; P = 0.573; OR = 1.23; 95% CI, 1.02-1.48; P = 0.029; and OR = 1.07; 95% CI, 0.88-1.29; P = 0.506.

IMPLICATIONS

The results suggest that treatment with belimumab plus standard therapy is more effective than placebo plus standard therapy in SLE patients, which represents major progress in the treatment of SLE. Regardless of the statistical analyses, further research is necessary to optimize treatment effects.

摘要

目的

近年来,对系统性红斑狼疮(SLE)患者使用贝利木单抗联合标准疗法进行了广泛研究。我们的目的是评估该疗法与安慰剂联合标准疗法相比,在SLE患者中的疗效和安全性。

方法

检索了PubMed、科学网、Embase、中国生物医学文献数据库(CBM,中文)和万方数据库(中文),查找2015年6月之前主要研究贝利木单抗联合标准疗法疗效和安全性的所有随机临床试验。我们提取或计算了所有纳入研究中52周时的SLE反应指数率和不良事件率。本荟萃分析中两组之间的比值比(OR)及其95%置信区间(CI)采用随机效应模型进行计算。还进行了敏感性和发表偏倚分析。所有统计检验均使用Stata软件12.0版(StataCorp.,德克萨斯州大学城)进行。

结果

在总体样本(4项研究,N = 4692)中,所有研究均显示,与安慰剂联合标准疗法组相比,贝利木单抗联合标准疗法组在52周时的SLE反应指数率显著更高(OR = 1.49;95%CI,1.26 - 1.77;P < 0.001)。在评估严重不良事件发生率时,数据显示两组之间无显著差异,合并OR = 1.08;95%CI,0.83 - 1.39;P = 0.573;OR = 1.23;95%CI,1.02 - 1.48;P = 0.029;OR = 1.07;95%CI,0.88 - 1.29;P = 0.506。

结论

结果表明,贝利木单抗联合标准疗法治疗SLE患者比安慰剂联合标准疗法更有效,这代表了SLE治疗的重大进展。无论统计分析结果如何,都需要进一步研究以优化治疗效果。

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