The effect of indacaterol/glycopyrronium versus tiotropium or salmeterol/fluticasone on the prevention of clinically important deterioration in COPD

被引:37
|
作者
Anzueto, Ntonio R. [1 ,2 ]
Vogelmeier, Claus F. [3 ]
Kostikas, Konstantinos [4 ]
Mezzi, Karen [4 ]
Fucile, Sebastian [5 ]
Bader, Giovanni [4 ]
Shen, Steven [5 ]
Banerji, Donald [5 ]
Fogel, Robert [5 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA
[2] Univ Texas San Antonio, South Texas Vet Healthcare Syst, San Antonio, TX USA
[3] Philipps Univ Marburg, Dept Med Pulm & Crit Care Med, Univ Med Ctr Giessen & Marburg, Marburg, Germany
[4] Novartis Pharma AG, Basel, Switzerland
[5] Novartis Pharmaceut, 1 Hlth Plaza, E Hanover, NJ 07936 USA
来源
INTERNATIONAL JOURNAL OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE | 2017年 / 12卷
关键词
IND/GLY; deterioration; COPD; OBSTRUCTIVE PULMONARY-DISEASE; SALMETEROL-FLUTICASONE; PARALLEL-GROUP; HEALTH-STATUS; LUNG-FUNCTION; DOUBLE-BLIND; QVA149; UMECLIDINIUM/VILANTEROL; GLYCOPYRRONIUM; EXACERBATIONS;
D O I
10.2147/COPD.S133307
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Endpoints that evaluate deterioration rather than improvement of disease may have clinical utility in COPD. In this analysis, we compared the effects of different maintenance treatments on the prevention of clinically important deterioration (CID) in moderate-to-severe COPD patients. Methods: Data were analyzed from three 26-week studies comparing indacaterol/ glycopyrronium (IND/GLY) with tiotropium (TIO) or salmeterol/fluticasone (SFC). Two definitions of CID were used; each was a composite of three outcome measures typically associated with COPD. Definition 1 (D1) comprised a >= 100 mL decrease in forced expiratory volume in 1 second (FEV1), a >= 4-unit increase in St George's Respiratory Questionnaire, and a moderate-to-severe COPD exacerbation. In Definition 2 (D2), a >= 1-unit decrease in transition dyspnea index replaced FEV1. Results: Using D1, IND/GLY significantly reduced the risk of first or sustained CID versus either TIO (hazard ratio 0.72 [0.61, 0.86], P=0.0003 and 0.73 [0.61, 0.89], P=0.001) or SFC (0.67 [0.57, 0.80] and 0.63 [0.52, 0.77], both P<0.0001). With D2, IND/GLY significantly reduced the risk of first, but not sustained, CID versus TIO (0.80 [0.64 to 0.99], P=0.0359 and 0.85 [0.66, 1.10], P=0.2208) and both first and sustained CID versus SFC (0.73 [0.61, 0.88], P=0.001 and 0.72 [0.58, 0.90], P=0.0036). Conclusion: These data confirm the utility of the CID endpoint as a means of monitoring COPD worsening in patients with moderate-to-severe COPD. Using the CID measure, we demonstrated that dual bronchodilation with IND/GLY significantly reduced the risk of CID versus either long-acting muscarinic antagonist or long-acting beta(2)-agonist/inhaled corticosteroid treatment, providing further evidence for the benefit of dual bronchodilation in this patient population.
引用
收藏
页码:1325 / 1337
页数:13
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