Queen's University and Kingston General Hospital, Kingston, Ontario K7L 2V7, Canada.
Respir Med. 2011 Jul;105(7):1030-6. doi: 10.1016/j.rmed.2011.03.014. Epub 2011 Apr 16.
Indacaterol is a novel, inhaled, once-daily ultra long-acting β(2)-agonist (ultra-LABA) for the treatment of COPD. This study investigated the effect of indacaterol on exercise endurance, and on lung hyperinflation during exercise and at rest in patients with moderate-to-severe COPD.
In this double-blind, placebo-controlled, two-period crossover study (3-week treatment, 3-week washout between treatments), patients were randomized to receive indacaterol 300 μg once-daily or matching placebo. The primary efficacy variable was exercise endurance time after 3 weeks of treatment, measured through constant-load cycle ergometry testing performed at 75% of the peak work rate in a screening incremental exercise test.
Of 90 patients randomized (mean age: 62.8 years; post-bronchodilator FEV(1): 61.2% predicted and FEV(1)/FVC: 51.6%), 74 completed the study. Pre-treatment exercise tolerance averaged 459 s. Improvement in exercise endurance time was higher with indacaterol 300 μg than with placebo both after the first dose (treatment difference: 101 s; p < 0.001) and after 3 weeks (treatment difference: 111 s; p = 0.011). In addition, indacaterol increased end-exercise inspiratory capacity (IC) versus placebo after 3 weeks (0.28 L, p = 0.002). Significant improvements were also observed in resting IC (0.17 L, p = 0.001), FEV(1) (0.25 L, p < 0.001) and FVC (0.26 L, p < 0.001) with indacaterol compared with placebo at 75 min post-dose after 3 weeks.
In conclusion, indacaterol treatment improved the ability of patients with COPD to exercise. In addition, the improvements observed in resting and end-exercise IC indicate reductions in lung hyperinflation after 3 weeks treatment (ClinicalTrials.gov registration number: NCT00620022).
茚达特罗是一种新型、每日一次吸入的长效β2-激动剂(ultra-LABA),用于治疗 COPD。本研究旨在探讨茚达特罗对 COPD 患者运动耐力的影响,以及对运动中和运动后静息时的肺过度充气的影响。
这是一项双盲、安慰剂对照、两周期交叉研究(3 周治疗,治疗之间 3 周洗脱期),患者被随机分配接受茚达特罗 300μg 每日一次或匹配安慰剂。主要疗效变量是经过 3 周治疗后,在筛选递增运动试验中以 75%的峰值做功率进行的恒负荷循环测功机测试后的运动耐力时间。
90 例随机患者(平均年龄:62.8 岁;支气管扩张剂后 FEV1:61.2%预测值和 FEV1/FVC:51.6%)中,74 例完成了研究。治疗前运动耐量平均为 459 秒。与安慰剂相比,茚达特罗 300μg 在第一次给药后(治疗差异:101 秒;p<0.001)和 3 周后(治疗差异:111 秒;p=0.011)均提高了运动耐力时间。此外,与安慰剂相比,茚达特罗在 3 周后增加了运动终末吸气量(IC)(0.28L,p=0.002)。与安慰剂相比,在 3 周后 75 分钟时,茚达特罗还显著改善了静息 IC(0.17L,p=0.001)、FEV1(0.25L,p<0.001)和 FVC(0.26L,p<0.001)。
总之,茚达特罗治疗改善了 COPD 患者的运动能力。此外,静息和运动终末 IC 的改善表明,经过 3 周治疗后,肺过度充气减少(临床试验注册编号:NCT00620022)。