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Once-daily fluticasone furoate is efficacious in patients with symptomatic asthma on low-dose inhaled corticosteroids
被引:43
|作者:
Bleecker, Eugene R.
[1
]
Bateman, Eric D.
[2
]
Busse, William W.
[3
]
Woodcock, Ashley
[4
]
Frith, Lucy
[5
]
House, Karen W.
[6
]
Jacques, Loretta
[5
]
Davis, Angela M.
[6
]
Haumann, Brett
[5
,7
]
Lotvall, Jan
[8
]
机构:
[1] Wake Forest Univ Hlth Sci, Ctr Genom & Personalized Med Res, Winston Salem, NC 27157 USA
[2] Univ Cape Town, Dept Med, ZA-7925 Cape Town, South Africa
[3] Univ Wisconsin, Dept Med, Madison, WI USA
[4] Univ Manchester, Sch Translat Med, Manchester Acad Hlth Sci Ctr, Manchester, Lancs, England
[5] GlaxoSmithKline, Resp Med Dev Ctr, London, England
[6] GlaxoSmithKline, Resp Med Dev Ctr, Res Triangle Pk, NC USA
[7] Circassia, Oxford, England
[8] Univ Gothenburg, Krefting Res Ctr, Gothenburg, Sweden
关键词:
PERSISTENT ASTHMA;
NOCTURNAL ASTHMA;
REFERENCE VALUES;
SINGLE INHALER;
BUDESONIDE;
PROPIONATE;
SALMETEROL;
ADHERENCE;
THERAPY;
POWDER;
D O I:
10.1016/j.anai.2012.08.017
中图分类号:
R392 [医学免疫学];
学科分类号:
100102 ;
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 mu g/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 mu g) once daily in the evening, FP 250 mu g 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 (FEV1) 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 FEV1. 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 mu g once daily, although statistically significant improvements versus placebo in symptom-free 24-hour periods were only reported for FF 400 mu g. 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 mu g once daily in the evening is effective and well tolerated in patients with asthma uncontrolled on low-dose ICS, with 100 mu g and 200 mu g, considered the most applicable doses in this asthma population. Trial Registration: clinicaltrials.gov Identifier: NCT00603278. (C) 2012 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
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页码:353 / +
页数:10
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