1 Weill Cornell University, New York, New York.
2 LungenClinic Grosshansdorf, Großhansdorf, Germany.
Am J Respir Crit Care Med. 2016 Sep 1;194(5):559-67. doi: 10.1164/rccm.201607-1349OC.
Moderate and severe exacerbations are incompletely prevented by maximal inhalation therapy in patients with severe chronic obstructive pulmonary disease.
To determine whether roflumilast reduces moderate and/or severe chronic obstructive pulmonary disease exacerbations in patients at risk for exacerbations despite treatment with inhaled corticosteroid/long-acting β2-agonist with or without a long-acting muscarinic antagonist (LAMA).
In this 52-week, phase 4, double-blind, placebo-controlled RE(2)SPOND (Roflumilast Effect on Exacerbations in Patients on Dual [LABA/ICS] Therapy) trial (NCT01443845), participants aged 40 years or older with severe/very severe chronic obstructive pulmonary disease, chronic bronchitis, two or more exacerbations and/or hospitalizations in the previous year, and receiving inhaled corticosteroid/long-acting β2-agonist with or without LAMA daily for 3 or more months were equally randomized to once-daily roflumilast, 500 μg (n = 1,178), or placebo (n = 1,176). Stratification was based on LAMA use.
Although rate of moderate or severe exacerbations per patient per year (primary endpoint) was reduced by 8.5% with roflumilast versus placebo, the between-group difference was not statistically significant (rate ratio, 0.92; 95% confidence interval, 0.81-1.04; P = 0.163). However, roflumilast improved lung function, and in a post hoc analysis roflumilast significantly reduced the rate of moderate or severe exacerbations in participants with a history of more than three exacerbations and/or one or more hospitalizations in the prior year. Adverse event-related discontinuations occurred in 11.7% roflumilast-treated and 5.4% placebo-treated participants. Deaths occurred in 2.5% roflumilast and 2.1% placebo participants.
Roflumilast failed to statistically significantly reduce moderate and/or severe exacerbations in the overall population. Roflumilast improved lung function and reduced exacerbations in participants with frequent exacerbations and/or hospitalization history. The safety profile of roflumilast was consistent with that of previous studies. Clinical trial registered with www.clinicaltrials.gov (NCT01443845).
在患有严重慢性阻塞性肺疾病的患者中,最大吸入疗法并不能完全预防中度和重度恶化。
确定罗氟司特是否可以减少有恶化风险的患者的中度和/或重度慢性阻塞性肺疾病恶化,这些患者尽管接受了吸入皮质类固醇/长效β2-激动剂联合或不联合长效抗胆碱能药物(LAMA)治疗。
在这项为期 52 周、4 期、双盲、安慰剂对照的 RE(2)SPOND(罗氟司特对接受双重[LABA/ICS]治疗的患者恶化的影响)试验(NCT01443845)中,年龄在 40 岁或以上的参与者患有严重/极严重的慢性阻塞性肺疾病、慢性支气管炎、过去一年中有两次或两次以上恶化和/或住院治疗,并且每天接受吸入皮质类固醇/长效β2-激动剂联合或不联合 LAMA 治疗至少 3 个月,随机分为每日一次罗氟司特 500μg(n=1178)或安慰剂(n=1176)。分层基于 LAMA 的使用情况。
尽管每年每患者的中度或重度恶化率(主要终点)与安慰剂相比降低了 8.5%,但组间差异无统计学意义(比率比,0.92;95%置信区间,0.81-1.04;P=0.163)。然而,罗氟司特改善了肺功能,并且在事后分析中,罗氟司特显著降低了既往有三次以上恶化和/或一年中一次或多次住院史的参与者的中度或重度恶化率。与不良事件相关的停药事件发生在 11.7%接受罗氟司特治疗的参与者和 5.4%接受安慰剂治疗的参与者中。死亡发生在 2.5%接受罗氟司特治疗的参与者和 2.1%接受安慰剂治疗的参与者中。
罗氟司特在总体人群中未能显著降低中度和/或重度恶化。罗氟司特改善了肺功能,并减少了频繁恶化和/或有住院史的参与者的恶化。罗氟司特的安全性与以往研究一致。该临床试验已在 www.clinicaltrials.gov 上注册(NCT01443845)。