Jorge Sinclair De Frías, Agostina Velo, Lorenzo Olivero, Abdul Rehman, Avinash Singh, David J Steiger
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引用次数: 0
Abstract
Introduction: Up to 40% of patients with COPD have an eosinophilic phenotype, which increases the risk of acute exacerbations. Mepolizumab, an anti - IL-5 monoclonal antibody, has shown mixed results. We conducted a systematic review and meta-analysis to evaluate the efficacy and safety of mepolizumab 100 mg in eosinophilic COPD.
Methods: Following PRISMA and Cochrane guidelines, we searched PubMed, Embase, and Cochrane Central through 18 May 2025. Randomized controlled trials comparing mepolizumab 100 mg versus placebo in eosinophilic COPD were included. The primary outcome was the annualized rate of moderate or severe exacerbations. Data were pooled using random-effects models.
Results: Four RCTs (1,953 patients) were included. Mepolizumab reduced annualized rate of moderate or severe exacerbations (Rate Ratio 0.80; 95% CI: 0.73-0.89; p < 0.00001) and prolonged time to first exacerbation (HR 0.78; 95% CI: 0.69-0.88; p < 0.0001). Sensitivity analysis excluding METREX showed fewer exacerbations requiring ED visits or hospitalization (Rate Ratio 0.63; 95% CI: 0.46-0.86; p = 0.004). Patient-reported outcomes did not improve. Safety was favorable, with reduced serious adverse events, including deaths (RR 0.84; 95% CI: 0.73-0.98; p = 0.03).
Conclusions: Mepolizumab reduces exacerbations with good safety in eosinophilic COPD, though without improvement in quality-of-life outcomes.
高达40%的COPD患者具有嗜酸性粒细胞表型,这增加了急性加重的风险。Mepolizumab是一种抗IL-5单克隆抗体,其结果喜忧参半。我们进行了一项系统回顾和荟萃分析,以评估mepolizumab 100mg治疗嗜酸性COPD的疗效和安全性。方法:按照PRISMA和Cochrane指南,检索PubMed、Embase和Cochrane Central至2025年5月18日。纳入了比较mepolizumab 100mg与安慰剂治疗嗜酸性COPD的随机对照试验。主要终点是中度或重度恶化的年化率。使用随机效应模型汇总数据。结果:纳入4项随机对照试验(1953例)。Mepolizumab降低了中度或重度恶化的年化率(比率比0.80;95% CI: 0.73-0.89; p p p = 0.004)。患者报告的结果没有改善。安全性良好,包括死亡在内的严重不良事件减少(RR 0.84; 95% CI: 0.73-0.98; p = 0.03)。结论:Mepolizumab可降低嗜酸性粒细胞性COPD患者的急性加重,安全性良好,但没有改善生活质量。