Division of Respiratory Medicine, Department of Medicine, University of Toronto, Toronto, Ontario, Canada
Division of Pulmonology and UCT Lung Institute, Department of Medicine, University of Cape Town, Cape Town, South Africa.
BMJ Open Respir Res. 2021 Aug;8(1). doi: 10.1136/bmjresp-2020-000819.
Despite currently available standard-of-care inhaled corticosteroid (ICS)/long-acting β-agonist therapies, a substantial proportion of patients with asthma remain inadequately controlled. This pooled analysis evaluated efficacy and safety of mometasone furoate/indacaterol acetate (MF/IND) versus fluticasone propionate/salmeterol xinafoate (FLU/SAL) in patients with inadequately controlled asthma.
This analysis included patients from PALLADIUM (NCT02554786) and IRIDIUM (NCT02571777) studies who received high-dose MF/IND (320/150 µg) or medium-dose MF/IND (160/150 µg) one time a day or high-dose FLU/SAL (500/50 µg) two times a day for 52 weeks. Reduction in asthma exacerbations, improvement in lung function, asthma control, and safety were evaluated for 52 weeks.
In total, 3154 patients (high-dose MF/IND, n=1054; medium-dose MF/IND, n=1044; high-dose FLU/SAL, n=1056) were included. High-dose MF/IND showed 26%, 22% and 19% reductions in rate of severe, moderate or severe, and all (mild, moderate and severe) exacerbations versus high-dose FLU/SAL, respectively, over 52 weeks (all, p<0.05). High-dose MF/IND improved trough FEV versus high-dose FLU/SAL at weeks 26 (Δ, 43 mL, p=0.001) and 52 (Δ, 51 mL, p<0.001). Reductions in asthma exacerbation rate and improvement in trough FEV with medium-dose MF/IND were comparable with high-dose FLU/SAL over 52 weeks. All treatments improved Asthma Control Questionnaire-7 score from baseline to 52 weeks with no difference between treatments. Safety was comparable between high-dose MF/IND and high-dose FLU/SAL.
One time a day, single-inhaler, high-dose MF/IND reduced asthma exacerbations and improved lung function versus two times a day, high-dose FLU/SAL in patients with inadequately controlled asthma. Similarly, improved outcomes were seen with one time a day, medium-dose MF/IND and two times a day, high-dose FLU/SAL, but at a lower ICS dose.
尽管目前有标准的吸入性皮质类固醇(ICS)/长效β激动剂疗法,但仍有相当一部分哮喘患者控制不佳。本汇总分析评估了中剂量糠酸莫米松/茚达特罗(MF/IND)与丙酸氟替卡松/沙美特罗(FLU/SAL)在控制不佳的哮喘患者中的疗效和安全性。
本分析纳入了 PALLADIUM(NCT02554786)和 IRIDIUM(NCT02571777)研究的患者,他们接受了高剂量 MF/IND(320/150μg)或中剂量 MF/IND(160/150μg)每日一次,或高剂量 FLU/SAL(500/50μg)每日两次,治疗 52 周。评估了 52 周内哮喘恶化的减少、肺功能的改善、哮喘控制和安全性。
共有 3154 名患者(高剂量 MF/IND,n=1054;中剂量 MF/IND,n=1044;高剂量 FLU/SAL,n=1056)被纳入。高剂量 MF/IND 与高剂量 FLU/SAL 相比,52 周内严重、中度或重度以及所有(轻度、中度和重度)恶化的发生率分别降低了 26%、22%和 19%(均,p<0.05)。高剂量 MF/IND 在 26 周(Δ,43 mL,p=0.001)和 52 周(Δ,51 mL,p<0.001)时改善了谷值 FEV 与高剂量 FLU/SAL。52 周时,中剂量 MF/IND 与高剂量 FLU/SAL 相比,哮喘恶化率降低和谷值 FEV 改善的情况相当。所有治疗均从基线改善了哮喘控制问卷-7 评分至 52 周,治疗之间无差异。高剂量 MF/IND 与高剂量 FLU/SAL 的安全性相当。
在控制不佳的哮喘患者中,每日一次、单吸入器高剂量 MF/IND 与每日两次、高剂量 FLU/SAL 相比,降低了哮喘恶化率并改善了肺功能。同样,每日一次、中剂量 MF/IND 与每日两次、高剂量 FLU/SAL 也观察到了改善的结果,但 ICS 剂量较低。