Maintenance of asthma control by once-daily inhaled ciclesonide in adults with persistent asthma

被引:91
作者
Chapman, KR
Patel, P
D'Urzo, AD
Alexander, M
Mehra, S
Oedekoven, C
Engelstätter, R
Boulet, LP
机构
[1] Univ Hlth Network, Toronto Western Hosp, Toronto, ON, Canada
[2] Allied Res Int, Mississauga, ON, Canada
[3] Primary Care Lung Clin, Toronto, ON, Canada
[4] Allied Hlth Ctr, Niagara Falls, ON, Canada
[5] Oshawa Clin, Oshawa, ON, Canada
[6] Altana Pharma AG, Constance, Germany
[7] Univ Laval, Hop Laval, Inst Cardiol & Pneumol, Quebec City, PQ, Canada
关键词
asthma; ciclesonide; cortisol; inhaled corticosteroids; safety;
D O I
10.1111/j.1398-9995.2004.00750.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Inhaled corticosteroids (ICS) are recommended therapy for persistent asthma, although side effects can limit appropriate use. Ciclesonide, a novel ICS, is activated in the lung, thereby reducing systemic activity and side effects. This 12-week, double-blind, randomized, parallel-group, placebo-controlled study evaluated the efficacy and safety of ciclesonide in adults with persistent asthma. Methods: After a 2-week baseline period in which current ICS treatment was continued, 329 patients were randomized to receive ciclesonide 160 mug (n=107) or 640 mug (n=112) (ex-actuator doses, equivalent to 200 and 800 mug ex-valve, respectively), or placebo (n=110) once daily in the morning. Efficacy was monitored by asthma symptom scores, rescue medication use, morning and evening peak expiratory flow (PEF) measurements, spirometry, and probability of study completion without experiencing lack of efficacy. Results: Morning PEF remained stable with either ciclesonide dose but decreased with placebo; the differences were significant (P<0.0001) for both ciclesonide doses vs placebo. The forced expiratory volume in 1 s and forced vital capacity decreased significantly with placebo (P<0.005), but were unchanged with ciclesonide. Lack of efficacy was significantly greater for patients switched to placebo (63%) than it was for those treated with ciclesonide 160 mug (30%) (P<0.0001 vs placebo) or ciclesonide 640 mug (31%) (P<0.0001 vs placebo). There were no significant differences between the two tested doses of ciclesonide with respect to efficacy and safety. Serum and 24-h urine cortisol were unaffected by ciclesonide treatment. Both doses of ciclesonide were well tolerated with no cases of oral candidiasis. Conclusion: Ciclesonide (160 or 640 mug) once daily in the morning effectively maintains asthma control, does not affect cortisol levels, and has an adverse event profile comparable with placebo in adults with primarily mild to moderate asthma.
引用
收藏
页码:330 / 337
页数:8
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