A pooled analysis of FEV1, decline in COPD patients randomized to inhaled corticosteroids or placebo

被引:107
作者
Soriano, Joan B.
Sin, Don D.
Zhang, Xuekui
Camp, Pat G.
Anderson, Julie A.
Anthonisen, Nick R.
Buist, A. Sonia
Burge, P. Sherwood
Calverley, Peter M.
Connett, John E.
Petersson, Stefan
Postma, Dirkje S.
Szafranski, Wojciech
Vestbo, Jorgen
机构
[1] Recinte Hosp Joan March, Program Epidemiol & Clin Res, Fdn Caubet, CIMERA Illes Balears,Int Ctr Adv Resp Med, Bunyola 07110, Mallorca, Spain
[2] St Pauls Hosp, James Hogg iCAPTURE Ctr Cardiovasc & Pulm Res, Vancouver, BC V6Z 1Y6, Canada
[3] GlaxoSmithKline R&D, Dept Stat, Greenford, Middx, England
[4] Univ Manitoba, Dept Med, Winnipeg, MB, Canada
[5] Oregon Hlth & Sci Univ, Dept Med, Portland, OR 97201 USA
[6] Heartlands Hosp NHS Trust, Dept Resp Med, Birmingham, W Midlands, England
[7] Aintree Univ Hosp NHS Fdn Trust, Dept Med, Liverpool, Merseyside, England
[8] Univ Minnesota, Sch Publ Hlth, Div Biostat, Minneapolis, MN 55455 USA
[9] AstraZeneca R&D, Dept Stat, Lund, Sweden
[10] Univ Groningen, Univ Med Ctr Groningen, Dept Pulmonol, Groningen, Netherlands
[11] Voivodeship Specialist Hosp, Dept Lung Dis, Radom, Poland
[12] S Manchester Univ Hosp NHS Trust, Wythenshawe Hosp, NW Lung Ctr, Manchester, Lancs, England
基金
加拿大健康研究院;
关键词
COPD; corticosteroids; FEV1; natural history; pooled analysis;
D O I
10.1378/chest.06-1696
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: There is controversy about whether therapy with inhaled corticosteroids (ICSs) modifies the natural history of COPD, characterized by an accelerated decline in FEV1. Methods: The Inhaled Steroids Effect Evaluation in COPD (ISEEC) study is a pooled study of patient-level data from seven long-term randomized controlled trials of ICS vs placebo lasting >= 12 months in patients with moderate-to-severe COPD. We have previously reported a survival benefit for ICS therapy in COPD patients using ISEEC data. We aimed to determine whether the regular use of ICSs vs placebo improves FEV1 decline in COPD patients, and whether this relationship is modified by gender and smoking. Results: There were 3,911 randomized participants (29.2% female) in this analysis. In the first 6 months after randomization, ICS use was associated with a significant mean (+/- SE) relative increase in FEV1 of 2.42 +/- 0.19% compared with placebo (p < 0.01), which is quantifiable in absolute terms as 42 mL in men and 29 mL in women over 6 months. From 6 to 36 months, there was no significant difference between placebo and ICS therapy in terms of FEV1 decline (-0.01 +/- 0.09%; p = 0.86). The initial treatment effect was dependent on smoking status and gender. Smokers who continued to smoke had a smaller increase in FEV1 during the first 6 months than did ex-smokers. Female ex-smokers had a larger increase in FEV1 with ICS therapy than did male ex-smokers. Conclusions: We conclude that in COPD in the first 6 months of treatment, ICS therapy is more effective in ex-smokers than in current smokers with COPD in improving lung function, and women may have a bigger response to ICSs than men. However, it seems that after 6 months, ICS therapy does not modify the decline in FEV1 among those who completed these randomized clinical trials.
引用
收藏
页码:682 / 689
页数:8
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