Efficacy and Safety of Mepolizumab in Eosinophilic COPD: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.

IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Annals of Pharmacotherapy Pub Date : 2026-11-01 Epub Date: 2026-04-26 DOI:10.1177/10600280261437728
Rahul Bisht, Arusha Desai, Esteban Marcelo Mogrovejo Carrión, Anjali Bhardwaj, Sidharth Misra, Tejesh Bangalore Shivashankar, Ramita Gupta
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引用次数: 0

Abstract

Objective: To evaluate the efficacy and safety of mepolizumab, a humanized monoclonal antibody that targets interleukin-5, a key mediator in eosinophilic inflammation, in reducing moderate-to-severe exacerbations among patients with eosinophilic chronic obstructive pulmonary disease (COPD).

Data sources: PubMed, Scopus, Web of Science, and Cochrane databases were systematically searched using the terms: "Mepolizumab," "COPD," "Chronic Obstructive Pulmonary Disease," for randomized controlled trials comparing subcutaneous mepolizumab (100 mg every 4 weeks) with placebo in patients with eosinophilic COPD from inception till July 2025.

Study selection and data extraction: Randomized controlled trials comparing subcutaneous mepolizumab with placebo in adults with eosinophilic COPD were included. Two independent reviewers screened studies and extracted data. Finally, 4 studies with a total of 1953 patients were included. Of these, 978 (50.0%) received mepolizumab.

Data synthesis: Statistical analysis was performed using R software (version 4.5.0). Mepolizumab significantly prolonged the time to first moderate or severe exacerbation (hazard ratio [HR] = 0.80; 95% confidence interval [CI] 0.69-0.92; P = 0.016) and reduced the rate of moderate-to-severe exacerbations (rate ratio 0.80; 95% CI 0.78-0.83; P < 0.001). The risk of adverse events (AEs) (risk ratio [RR] = 1.00; 95% CI 0.95-1.06; P = 0.962) was similar between groups, while the risk of serious adverse events or death (RR = 0.83; 95% CI 0.72-0.96; P = 0.031) was significantly lower in the mepolizumab group.Relevance to Patient Care and Clinical Practice in Comparison With Existing Drugs:Mepolizumab provides a targeted, biomarker-guided treatment option, potentially reducing exacerbations without the added safety concerns like infections and metabolic complications as seen with existing therapies.

Conclusion and relevance: Mepolizumab reduces the time to first moderate or severe exacerbation and prolongs symptom-free periods in patients with eosinophilic COPD, without increasing the risk of AEs.

Mepolizumab治疗嗜酸性COPD的疗效和安全性:随机对照试验的系统评价和荟萃分析
目的:评估mepolizumab的有效性和安全性,mepolizumab是一种针对白细胞介素-5的人源化单克隆抗体,白细胞介素-5是嗜酸性粒细胞炎症的关键介质,可减少嗜酸性粒细胞慢性阻塞性肺疾病(COPD)患者中至重度加重。数据来源:PubMed, Scopus, Web of Science和Cochrane数据库系统地检索术语:“Mepolizumab”,“COPD”,“慢性阻塞性肺疾病”,用于比较从开始到2025年7月嗜酸性COPD患者皮下Mepolizumab(每4周100 mg)与安慰剂的随机对照试验。研究选择和数据提取:纳入了比较成人嗜酸性慢性阻塞性肺病患者皮下美polizumab与安慰剂的随机对照试验。两名独立审稿人筛选研究并提取数据。最后纳入4项研究,共纳入1953例患者。其中,978例(50.0%)接受了mepolizumab治疗。数据综合:采用R软件(4.5.0版本)进行统计分析。Mepolizumab显著延长了首次出现中度或重度恶化的时间(风险比[HR] = 0.80; 95%可信区间[CI] 0.69-0.92; P = 0.016),并降低了中度至重度恶化的发生率(发生率比0.80;95% CI 0.78-0.83; P < 0.001)。两组间不良事件(ae)发生风险(风险比[RR] = 1.00; 95% CI 0.95 ~ 1.06; P = 0.962)相似,而mepolizumab组严重不良事件或死亡风险(RR = 0.83; 95% CI 0.72 ~ 0.96; P = 0.031)显著降低。与现有药物相比,Mepolizumab与患者护理和临床实践的相关性:Mepolizumab提供了一种有针对性的、生物标志物引导的治疗选择,可能会减少病情恶化,而不会像现有疗法那样出现感染和代谢并发症等额外的安全问题。结论及相关性:Mepolizumab可减少嗜酸性COPD患者首次中度或重度加重的时间,延长无症状期,而不增加不良反应的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.70
自引率
0.00%
发文量
166
审稿时长
3-8 weeks
期刊介绍: Annals of Pharmacotherapy (AOP) is a peer-reviewed journal that advances pharmacotherapy throughout the world by publishing high-quality research and review articles to achieve the most desired health outcomes.The articles provide cutting-edge information about the most efficient, safe and cost-effective pharmacotherapy for the treatment and prevention of various illnesses. This journal is a member of the Committee on Publication Ethics (COPE). Average time from submission to first decision: 14 days
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