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首页> 外文期刊>Annals of allergy, asthma, and immunology >Once-daily fluticasone furoate is efficacious in patients with symptomatic asthma on low-dose inhaled corticosteroids
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Once-daily fluticasone furoate is efficacious in patients with symptomatic asthma on low-dose inhaled corticosteroids

机译:每天一次糠酸氟替卡松对有症状哮喘患者的小剂量吸入糖皮质激素有效

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摘要

Background: Fluticasone furoate (FF) is an inhaled corticosteroid (ICS) with 24-hour activity in development as a once-daily treatment for the long-term management of asthma. Objective: To assess the efficacy and safety of 4 doses of once-daily FF administered using a dry powder inhaler in patients (12 years) with moderate asthma, uncontrolled on low-dose ICS (fluticasone propionate [FP] 200 μg/day or equivalent). Methods: This double-blind, placebo-controlled, dose-ranging study randomized 622 patients to 1 of 6 treatments: FF (100, 200, 300, or 400 μg) once daily in the evening, FP 250 μg twice daily (active control), or placebo for 8 weeks. The primary endpoint was the change from baseline in predose evening forced expiratory colume in 1 second (FEV 1) at week 8. Results: At week 8, relative to placebo, all doses of FF once daily and FP twice daily demonstrated significantly (P .001) greater increases from baseline and greater than 200-mL increases in predose FEV 1. There was no evidence of a dose-response relationship between FF doses. Improvement with once-daily FF was similar to or greater than that for twice-daily FP. Secondary efficacy endpoint findings generally supported the efficacy of FF 100 to 400 μg once daily, although statistically significant improvements versus placebo in symptom-free 24-hour periods were only reported for FF 400 μg. There were few withdrawals due to lack of efficacy. Oral candidiasis was reported in 0 to 4% of patients; 24-hour urinary cortisol excretion ratios were similar across active treatment groups and not significantly different from placebo. Conclusion: FF 100 to 400 μg once daily in the evening is effective and well tolerated in patients with asthma uncontrolled on low-dose ICS, with 100 μg and 200 μg, considered the most applicable doses in this asthma population. Trial Registration: clinicaltrials.gov Identifier: NCT00603278.
机译:背景:糠酸氟替卡松(FF)是一种吸入性皮质类固醇(ICS),具有24小时的开发活动,可作为每日一次的哮喘长期治疗药物。目的:评估使用干粉吸入器每日4次FF的剂量和安全性,对中度哮喘患者(<12岁)使用低剂量ICS(丙酸氟替卡松[FP] 200μg/天或当量)。方法:这项双盲,安慰剂对照,剂量范围研究将622例患者随机分配至6种治疗方法之一:傍晚每天一次FF(100、200、300或400μg),每天两次两次FP 250μg(主动控制) )或安慰剂治疗8周。主要终点是在第8周的1秒钟用药前傍晚强迫呼气的血中基线相对变化(FEV 1)。结果:在第8周,相对于安慰剂,所有剂量的FF每天一次,FP每天两次,均具有显着性(P < 0.001)从基线开始有更大的增加,而剂量前FEV 1则增加了200-mL以上。没有证据表明FF剂量之间存在剂量反应关系。每天一次FF的改善与每天两次FP的改善相似或更大。次要疗效终点结果通常支持FF 100至400μg每天一次的疗效,尽管据报道仅在FF 400μg下无症状的24小时内与安慰剂相比有统计学显着改善。由于缺乏疗效而很少撤药。据报告0%至4%的患者存在口腔念珠菌病;活性治疗组的24小时尿皮质醇排泄率相似,与安慰剂无显着差异。结论:每天晚上一次100至400μgFF对于不受低剂量ICS控制的哮喘患者有效且耐受性良好,分别为100μg和200μg,被认为是该哮喘人群中最适用的剂量。试用注册:clinicaltrials.gov标识符:NCT00603278。

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