Effect of 1-year treatment with roflumilast in severe chronic obstructive pulmonary disease

被引:229
作者
Calverley, Peter M. A.
Sanchez-Torill, Fernando
McIvor, Andrew
Teichmann, Peter
Bredenbroeker, Dirk
Fabbri, Leonardo M.
机构
[1] Univ Liverpool, Aintree Hosp, Dept Med, Div Infect & Immun, Liverpool L69 3BX, Merseyside, England
[2] Hosp Arnau Vilanova, Valencia, Spain
[3] Queen Elizabeth 2 Hlth Sci Ctr, Halifax, NS, Canada
[4] Altana Pharma AG, Nycomed Grp, Constance, Germany
[5] Univ Modena, Dept Resp Dis, I-41100 Modena, Italy
关键词
antiinflammatory; chronic obstructive pulmonary disease; exacerbations; lung function; phosphodiesterase-4; inhibitor;
D O I
10.1164/rccm.200610-1563OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: The oral phosphodiesterase-4 (PDE4) inhibitor, roflumilast, can improve lung function in moderate chronic obstructive pulmonary disease (COPD). Whether treatment is effective in more severe COPD (GOLD [Global Initiative for Chronic Obstructive Lung Disease] stages III and IV) over a longer period is unknown. Objectives: To determine whether roflumilast improves lung function and decreases exacerbation frequency over 1 year in patients with stable COPD. Methods: We conducted a randomized, placebo-controlled, double-blind, parallel-group trial for I year. We recruited 1,513 patients (mean post-bronchodilator FEV, 41 % predicted), 760 receiving oral 500 mu g roflumilast and 753 receiving placebo once daily. Measurements and Main Results: We recorded post-bronchodilator FEV1, exacerbation rate, St. George's Respiratory Questionnaire total score at the study end point, and number and type of reported adverse events during treatment. Post-bronchodilator FEV, increased by 39 ml with roflumilast compared with placebo by 52 weeks (p = 0.001). The mean exacerbation rate was low and comparable in both treatment groups (0.86 vs. 0.92 exacerbation s/patient/yr for roflumilast and placebo, respectively). In a retrospective analysis, the exacerbation rate in patients in GOLD stage IV disease was 36% lower in patients treated with roflumilast than in those treated with placebo (1.01 vs. 1.59 exacerbations/patient/year, respectively; p = 0.024). The St. George's Respiratory Questionnaire total score did not differ between treatments. The commonest adverse events related to roflumilast treatment were diarrhea, nausea, and headache, which usually subsided during continued treatment. However, roflumilast resulted in more withdrawals within the first 3 to 4 weeks of administration. Conclusions: In severe, stable COPD, PDE4 inhibition with roflumilast produced a modest but significant improvement in lung function without changing the exacerbation rate or health status. However, patients with very severe disease experienced fewer exacerbations with roflumilast.
引用
收藏
页码:154 / 161
页数:8
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