Efficacy of once-daily, single-inhaler, fixed-dose combination of mometasone/indacaterol/glycopyrronium in patients with asthma with or without persistent airflow limitation: Post hoc analysis from the IRIDIUM study

茚达特罗 医学 哮喘 析因分析 沙美特罗 皮质类固醇 支气管扩张剂 丙酸氟替卡松 氟替卡松 内科学 固定剂量组合 慢性阻塞性肺病 吸入器 麻醉
作者
Richard N. van Zyl-Smit,Huib A.M. Kerstjens,Jorge Máspero,Κonstantinos Κostikas,Motoi Hosoe,Ana- Maria Tanase,Peter D’Andrea,Karen Mezzi,Dominic E. A. Brittain,David Lawrence,Kenneth R. Chapman
出处
期刊:Respiratory Medicine [Elsevier BV]
卷期号:211: 107172-107172 被引量:2
标识
DOI:10.1016/j.rmed.2023.107172
摘要

BackgroundA novel, once-daily, fixed-dose combination of mometasone furoate/indacaterol acetate/glycopyrronium bromide (MF/IND/GLY) delivered via Breezhaler® is the first inhaled corticosteroid/long-acting ꞵ2-agonist/long-acting muscarinic antagonist (ICS/LABA/LAMA) therapy approved for the maintenance treatment of asthma in adults inadequately controlled on ICS/LABA combination. In patients with asthma and persistent airflow limitation (PAL), maximal treatment, especially with combination is suggested. This post hoc analysis of data from the IRIDIUM study assessed the efficacy of MF/IND/GLY in asthma patients with and without PAL.MethodsPatients with post-bronchodilator FEV1 ≤80% of predicted and FEV1/FVC ratio of ≤0.7 were categorised as PAL subgroup and the remaining as the non-PAL subgroup. Lung function parameters (FEV1, PEF, and FEF25%–75%) and annualised asthma exacerbations rates were evaluated in both subgroups across the treatment arms: once-daily high-dose MF/IND/GLY (160/150/50 μg), high-dose MF/IND (320/150 μg) and twice-daily high-dose fluticasone/salmeterol (FLU/SAL; 500/50 μg).ResultsOf the 3092 randomised patients, 64% (n = 1981) met the criteria for PAL. Overall, there was no evidence of treatment difference between PAL and non-PAL subgroups (interaction P-value for FEV1, FEF25%–75%, PEF, moderate or severe exacerbations, severe exacerbations and all exacerbations were 0.42, 0.08, 0.43 0.29, 0.35 and 0.12, respectively). In the PAL subgroup, high-dose MF/IND/GLY versus high-dose MF/IND and high-dose FLU/SAL improved trough FEV1 (mean difference: 102 mL [P < 0.0001] and 137 mL [P < 0.0001]) and reduced moderate or severe (16% and 32%), severe (25% and 39%) and all exacerbations (19% and 38%), respectively.ConclusionsOnce-daily fixed-dose MF/IND/GLY was efficacious in asthma patients with and without persistent airflow limitation.
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