Kyriakopoulos Christos, Papadopoulou Efthymia, Potonos Dimitrios, Exarchos Konstantinos, Beris Evangelos, Aggelopoulou Christina, Tryfon Stavros, Gogali Athena, Kostikas Konstantinos
Respiratory Medicine Department, Faculty of Medicine, University of Ioannina, Ioannina, Greece.
Respiratory Medicine Department, General Hospital of Thessaloniki G Papanikolaou, Thessaloniki, Greece.
ERJ Open Res. 2025 Mar 24;11(2). doi: 10.1183/23120541.00625-2024. eCollection 2025 Mar.
Three biologics targeting interleukin 5 (anti-IL-5) or its receptor-α (anti-IL-5Rα) are approved for patients with severe asthma.
We systematically searched the literature published in Medline and Embase up to 1 May 2023 to identify observational studies and nonrandomised trials that assess the response to anti-IL-5/5Rα in real-life patients with severe eosinophilic asthma. We also performed random-effects meta-analyses.
We identified 6401 studies, of which 92 with 9546 patients were analysed. Biologics use was associated with a 62% reduction in severe exacerbations (risk ratio 0.38, 95% CI 0.29-0.50) and a 54% reduction in hospitalisations (risk ratio 0.46, 95% CI 0.35-0.61) at 12 months of treatment, compared to pre-treatment. Biologics improved asthma control (decrease in asthma control questionnaire score by 1.11 points (95% CI -1.29--0.94) and increase in asthma control test score by 6.41 points (95% CI 5.66-7.16)) and increased the asthma quality of life questionnaire score by 1.08 points (95% CI 0.88-1.28) and forced expiratory volume in 1 s by 0.21 L (95% CI 0.15-0.27) at 12 months. There was a significant reduction in oral corticosteroids use of 51% (risk ratio 0.49, 95% CI 0.42-0.56), with a mean dose reduction of 6.01 mg·day (95% CI -7.55--4.48) at 12 months of treatment. Similar findings were observed at 3-4, 6 and 24 months. A biomarker-related response to treatment was also noted.
This comprehensive meta-analysis summarises the significant clinical response to anti-IL-5/5Rα biologics in real-life studies, providing important insights for their use in clinical practice.
三种靶向白细胞介素5(抗IL-5)或其受体α(抗IL-5Rα)的生物制剂已被批准用于重度哮喘患者。
我们系统检索了截至2023年5月1日发表在Medline和Embase上的文献,以确定评估重度嗜酸性粒细胞性哮喘患者在现实生活中对抗IL-5/5Rα反应的观察性研究和非随机试验。我们还进行了随机效应荟萃分析。
我们识别出6401项研究,其中对92项研究(共9546例患者)进行了分析。与治疗前相比,在治疗12个月时,使用生物制剂可使严重发作减少62%(风险比0.38,95%置信区间0.29 - 0.50),住院减少54%(风险比0.46,95%置信区间0.35 - 0.61)。生物制剂改善了哮喘控制(哮喘控制问卷评分降低1.11分(95%置信区间 - 1.29至 - 0.94),哮喘控制测试评分增加6.41分(95%置信区间5.66 - 7.16)),并使哮喘生活质量问卷评分在12个月时增加1.08分(95%置信区间0.88 - 1.28),第1秒用力呼气量增加0.21 L(95%置信区间0.15 - 0.27)。口服糖皮质激素的使用显著减少了51%(风险比0.49,95%置信区间0.42 - 0.56),在治疗12个月时平均剂量减少6.01 mg·天(95%置信区间 - 7.55至 - 4.48)。在3 - 4个月、6个月和24个月时观察到类似结果。还注意到与生物标志物相关的治疗反应。
这项全面的荟萃分析总结了现实生活研究中抗IL-5/5Rα生物制剂显著的临床反应,为其在临床实践中的应用提供了重要见解。