LABA/LAMA 与 LABA/ICS 固定剂量联合制剂在预防 COPD 加重中的作用:文献汇总数据的建模分析。
LABA/LAMA versus LABA/ICS fixed-dose combinations in the prevention of COPD exacerbations: a modeling analysis of literature aggregate data.
机构信息
Center for Drug Clinical Evaluation Shanghai, University of Traditional Chinese Medicine, No. 1200 Cailun Road, Shanghai, China.
出版信息
Eur J Clin Pharmacol. 2023 Oct;79(10):1321-1332. doi: 10.1007/s00228-023-03543-y. Epub 2023 Jul 29.
OBJECTIVES
This study aimed to quantitatively compare the efficacy and safety of long-acting β-agonist (LABA)/long-acting muscarinic antagonist (LAMA) and LABA/inhaled corticosteroid (ICS) fixed-dose combinations (FDCs) in preventing moderate or severe chronic obstructive pulmonary disease (COPD) exacerbations.
METHODS
A literature search was performed using public databases. The time course characteristics of the probability of a moderate or severe exacerbation in stable COPD patients treated with LABA/LAMA and LABA/ICS FDCs were described by the parametric survival function. A random-effects model in a single-arm meta-analysis was used to analyze the incidence of serious adverse events (SAEs) and pneumonia.
RESULTS
Twenty studies including 23,955 participants were included. The proportion of participants with a history of COPD exacerbation (%) in the previous year and the postbronchodilator forced expiratory volume in the first second (FEV) (%predicted) were important factors affecting drug efficacy. After adjusting the above factors to median levels of 100% and 45.5%, respectively, the moderate or severe exacerbation rates at 52 weeks for olodaterol/tiotropium, formoterol/budesonide, indacaterol/glycopyrronium, formoterol/glycopyrronium, vilanterol/fluticasone, salmeterol/fluticasone, and vilanterol/umeclidinium were 38.3%, 41.0%, 42.6%, 47.0%, 47.5%, 47.9%, and 53.0%, respectively. In terms of safety, significant differences were observed among drugs containing different LABA/LAMA FDCs.
CONCLUSIONS
This study showed that not all LABA/LAMA FDCs were superior to LABA/ICS FDCs in safety and in preventing moderate or severe exacerbations in patients with stable COPD, providing important quantitative information for COPD-related guidelines.
目的
本研究旨在定量比较长效β-激动剂(LABA)/长效抗胆碱能拮抗剂(LAMA)和 LABA/吸入性皮质类固醇(ICS)固定剂量组合(FDC)在预防中重度慢性阻塞性肺疾病(COPD)加重方面的疗效和安全性。
方法
使用公共数据库进行文献检索。采用参数生存函数描述稳定型 COPD 患者接受 LABA/LAMA 和 LABA/ICS FDC 治疗时中重度加重的概率随时间的变化特征。采用单臂荟萃分析的随机效应模型分析严重不良事件(SAE)和肺炎的发生率。
结果
共纳入 20 项研究,共计 23955 名参与者。既往 1 年 COPD 加重史的参与者比例(%)和支气管扩张剂后第一秒用力呼气容积(FEV)占预计值的百分比(%predicted)是影响药物疗效的重要因素。在分别调整上述因素至中位数水平(100%和 45.5%)后,52 周时 olodaterol/tiotropium、formoterol/budesonide、indacaterol/glycopyrronium、formoterol/glycopyrronium、vilanterol/fluticasone、salmeterol/fluticasone 和 vilanterol/umeclidinium 的中重度加重发生率分别为 38.3%、41.0%、42.6%、47.0%、47.5%、47.9%和 53.0%。安全性方面,不同 LABA/LAMA FDC 药物之间存在显著差异。
结论
本研究表明,并非所有 LABA/LAMA FDC 都在安全性和预防稳定型 COPD 患者中重度加重方面优于 LABA/ICS FDC,为 COPD 相关指南提供了重要的定量信息。