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噻托溴铵和奥达特罗预防慢性阻塞性肺疾病恶化(DYNAGITO):一项双盲、随机、平行分组、阳性对照试验。

Tiotropium and olodaterol in the prevention of chronic obstructive pulmonary disease exacerbations (DYNAGITO): a double-blind, randomised, parallel-group, active-controlled trial.

机构信息

Clinical Science Centre, Institute of Ageing and Chronic Disease, University of Liverpool, Liverpool, UK.

Department of Pulmonary Medicine and Critical Care, University of Texas Health Sciences Center and South Texas Veterans' Health Care System, San Antonio, TX, USA.

出版信息

Lancet Respir Med. 2018 May;6(5):337-344. doi: 10.1016/S2213-2600(18)30102-4. Epub 2018 Apr 5.

Abstract

BACKGROUND

Combinations of long-acting bronchodilators are recommended to reduce the rate of chronic obstructive pulmonary disease (COPD) exacerbations. It is unclear whether combining olodaterol, a long-acting beta-agonist, with tiotropium, a long-acting anti-muscarinic, reduces the rate of exacerbations compared with tiotropium alone.

METHODS

This 52-week, double-blind, randomised, parallel-group, active-controlled trial randomly assigned (1:1) patients with COPD with a history of exacerbations using a randomised block design to receive tiotropium-olodaterol 5 μg-5 μg or tiotropium 5 μg once daily. Patients using inhaled corticosteroids continued this therapy. Treatment was masked to patients, investigators, and those involved in analysing the data. The primary endpoint was the rate of moderate and severe COPD exacerbations from the first dose of medication until 1 day after last drug administration. The primary analysis included all randomly assigned patients who received any dose of study medication but were not from a site excluded due to on-site protocol violations. The trial is registered with ClinicalTrials.gov, number NCT02296138.

FINDINGS

Overall, 9009 patients were screened from 818 centres in 51 countries. We recruited 7880 patients between Jan 22, 2015 and March 7, 2016 (mean age 66·4 years [SD 8·5], 5626 [71%] were men, mean FEV percent predicted 44·5% [SD 27·7]): 3939 received tiotropium-olodaterol and 3941 tiotropium. The rate of moderate and severe exacerbations was lower with tiotropium-olodaterol than tiotropium (rate ratio [RR] 0·93, 99% CI 0·85-1·02; p=0·0498), not meeting the targeted 0·01 significance level. The proportion of patients reporting adverse events was similar between treatments.

INTERPRETATION

Combining tiotropium and olodaterol did not reduce exacerbation rate as much as expected compared with tiotropium alone.

FUNDING

Boehringer Ingelheim International GmbH.

摘要

背景

长效支气管扩张剂联合使用可降低慢性阻塞性肺疾病(COPD)恶化的发生率。长效β激动剂奥达特罗与长效抗毒蕈碱药物噻托溴铵联合使用是否能比单用噻托溴铵降低恶化发生率,目前尚不清楚。

方法

这是一项为期 52 周、双盲、随机、平行分组、阳性对照试验,采用随机区组设计,将有恶化史的 COPD 患者(1:1 随机分组)随机分配接受奥达特罗-噻托溴铵 5μg-5μg 或噻托溴铵 5μg 每日一次治疗。使用吸入性皮质类固醇的患者继续接受这种治疗。治疗对患者、研究者和参与数据分析的人员设盲。主要终点是从首次服药到最后一次给药后 1 天,中重度 COPD 恶化的发生率。主要分析纳入了所有接受任何剂量研究药物但因现场违反方案而未从现场排除的随机分配患者。该试验在 ClinicalTrials.gov 注册,编号为 NCT02296138。

结果

总体而言,在 51 个国家的 818 个中心,有 9009 名患者接受了筛选。我们于 2015 年 1 月 22 日至 2016 年 3 月 7 日期间招募了 7880 名患者(平均年龄 66.4 岁[标准差 8.5],5626 名[71%]为男性,平均 FEV%预测值 44.5%[标准差 27.7%]):3939 名患者接受奥达特罗-噻托溴铵治疗,3941 名患者接受噻托溴铵治疗。奥达特罗-噻托溴铵组中中重度恶化的发生率低于噻托溴铵组(比值比[RR]0.93,99%置信区间[CI]0.85-1.02;p=0.0498),未达到目标的 0.01 显著性水平。两种治疗的不良事件报告比例相似。

解释

与单用噻托溴铵相比,奥达特罗与噻托溴铵联合使用并未如预期般降低恶化发生率。

资助

勃林格殷格翰国际有限公司。

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