Inhaled Combined Budesonide-Formoterol as Needed in Mild Asthma

被引:411
|
作者
O'Byrne, Paul M. [1 ,2 ]
FitzGerald, J. Mark [3 ]
Bateman, Eric D. [4 ]
Barnes, Peter J. [5 ]
Zhong, Nanshan [6 ]
Keen, Christina [7 ]
Jorup, Carin [7 ]
Lamarca, Rosa [8 ]
Ivanov, Stefan [7 ]
Reddel, Helen K. [9 ]
机构
[1] McMaster Univ, St Josephs Healthcare, Firestone Inst Resp Hlth, Rm 2E1,1280 Main St West, Hamilton, ON L8S 4K1, Canada
[2] McMaster Univ, Michael G DeGroote Sch Med, Dept Med, Hamilton, ON, Canada
[3] Univ British Columbia, Inst Heart & Lung Hlth, Vancouver, BC, Canada
[4] Univ Cape Town, Dept Med, Div Pulmonol, Cape Town, South Africa
[5] Imperial Coll, Natl Heart & Lung Inst, Airway Dis Sect, London, England
[6] Guangzhou Med Univ, Affiliated Hosp 1, State Key Lab Resp Dis, Guangzhou, Guangdong, Peoples R China
[7] AstraZeneca Res & Dev, Gothenburg, Sweden
[8] AstraZeneca Res & Dev, Barcelona, Spain
[9] Univ Sydney, Woolcock Inst Med Res, Sydney, NSW, Australia
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2018年 / 378卷 / 20期
关键词
RANDOMIZED CONTROLLED-TRIAL; RELIEVER THERAPY; SINGLE INHALER; DOUBLE-BLIND; CLINICAL-TRIAL; MAINTENANCE; BUDESONIDE/FORMOTEROL; CORTICOSTEROIDS; EXACERBATIONS; COMBINATION;
D O I
10.1056/NEJMoa1715274
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND In patients with mild asthma, as-needed use of an inhaled glucocorticoid plus a fast-acting beta(2)-agonist may be an alternative to conventional treatment strategies. METHODS We conducted a 52-week, double-blind trial involving patients 12 years of age or older with mild asthma. Patients were randomly assigned to one of three regimens: twice-daily placebo plus terbutaline (0.5 mg) used as needed (terbutaline group), twice-daily placebo plus budesonide-formoterol (200 mu g of budesonide and 6 mu g of formoterol) used as needed (budesonide-formoterol group), or twice-daily budesonide (200 mu g) plus terbutaline used as needed (budesonide maintenance group). The primary objective was to investigate the superiority of as-needed budesonide-formoterol to as-needed terbutaline with regard to electronically recorded weeks with well-controlled asthma. RESULTS A total of 3849 patients underwent randomization, and 3836 (1277 in the terbutaline group, 1277 in the budesonide-formoterol group, and 1282 in the budesonide maintenance group) were included in the full analysis and safety data sets. With respect to the mean percentage of weeks with well-controlled asthma per patient, budesonide-formoterol was superior to terbutaline (34.4% vs. 31.1% of weeks; odds ratio, 1.14; 95% confidence interval [CI], 1.00 to 1.30; P = 0.046) but inferior to budesonide maintenance therapy (34.4% and 44.4%, respectively; odds ratio, 0.64; 95% CI, 0.57 to 0.73). The annual rate of severe exacerbations was 0.20 with terbutaline, 0.07 with budesonide-formoterol, and 0.09 with budesonide maintenance therapy; the rate ratio was 0.36 (95% CI, 0.27 to 0.49) for budesonide-formoterol versus terbutaline and 0.83 (95% CI, 0.59 to 1.16) for budesonide-formoterol versus budesonide maintenance therapy. The rate of adherence in the budesonide maintenance group was 78.9%. The median metered daily dose of inhaled glucocorticoid in the budesonide-formoterol group (57 mu g) was 17% of the dose in the budesonide maintenance group (340 mu g). CONCLUSIONS In patients with mild asthma, as-needed budesonide-formoterol provided superior asthma-symptom control to as-needed terbutaline, assessed according to electronically recorded weeks with well-controlled asthma, but was inferior to budesonide maintenance therapy. Exacerbation rates with the two budesonide-containing regimens were similar and were lower than the rate with terbutaline. Budesonide-formoterol used as needed resulted in substantially lower glucocorticoid exposure than budesonide maintenance therapy.
引用
收藏
页码:1865 / 1876
页数:12
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