Chiang Hsin-Yu, Guo Zi-An, Wu Ta-Wei, Peng Tzu-Rong
Department of Pharmacy, 145204Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City, Taiwan.
Lupus. 2022 May;31(6):666-673. doi: 10.1177/09612033221090888. Epub 2022 Mar 23.
Belimumab is the first biological agent approved for the treatment of systemic lupus erythematosus (SLE). The efficacy and safety of belimumab for SLE patients are not clear. Therefore, this meta-analysis is integrating the efficacy and safety of belimumab for patients with SLE.
PubMed, EMBASE, and Cochrane Library were searched for randomized clinical trials (RCTs) that studied the efficacy and safety of belimumab plus standard therapy before November 1, 2021. Data were pooled using the random-effects model and are expressed as risk ratios (RRs) or mean difference (MD) and corresponding 95% confidence intervals (CIs). Heterogeneity was assessed and quantified using .
Seven RCTs with 3,009 participants were included in this meta-analysis. Belimumab showed significantly decreased at least a 4-point improvement in Safety of Estrogen in Lupus National Assessment (SELENA)-Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) score than placebo (RR, 1.32; 95% CI, 1.21-1.44; < 0.001). However, belimumab significantly reduced the prednisone dose by 50% or more than placebo (RR, 1.59; 95% CI, 1.17-2.15; = 0.003) and belimumab significantly increased the 36 Physical Component Summary (PCS) score (MD, 1.60; 95% CI, 0.30-2.90; = 0.02). Regarding adverse events, there was no significant difference between the belimumab group and the control group.
The results suggest that belimumab plus standard therapy is more effective than placebo plus standard therapy in SLE patients.
贝利尤单抗是首个被批准用于治疗系统性红斑狼疮(SLE)的生物制剂。贝利尤单抗治疗SLE患者的疗效和安全性尚不清楚。因此,本荟萃分析旨在综合评估贝利尤单抗治疗SLE患者的疗效和安全性。
检索了PubMed、EMBASE和Cochrane图书馆中截至2021年11月1日研究贝利尤单抗联合标准治疗的疗效和安全性的随机临床试验(RCT)。使用随机效应模型汇总数据,并以风险比(RRs)或平均差(MD)及相应的95%置信区间(CIs)表示。使用 评估和量化异质性。
本荟萃分析纳入了7项RCT,共3009名参与者。贝利尤单抗组在狼疮国家评估(SELENA)-系统性红斑狼疮疾病活动指数(SLEDAI)评分上至少改善4分的比例显著高于安慰剂组(RR,1.32;95%CI,1.21-1.44;<0.001)。然而,贝利尤单抗组将泼尼松剂量显著降低50%以上的比例高于安慰剂组(RR,1.59;95%CI,1.17-2.15;=0.003),且贝利尤单抗组显著提高了36项身体成分总结(PCS)评分(MD,1.60;95%CI,0.30-2.90;=0.02)。关于不良事件,贝利尤单抗组与对照组之间无显著差异。
结果表明,在SLE患者中,贝利尤单抗联合标准治疗比安慰剂联合标准治疗更有效。