Calverley Peter Ma, Page Clive, Dal Negro Roberto W, Fontana Giovanni, Cazzola Mario, Cicero Arrigo F, Pozzi Edoardo, Wedzicha Jadwiga A
Department of Medicine, Clinical Sciences Centre, University Hospital Aintree, Liverpool, UK.
Faculty of Life Sciences and Medicine, King's College, London, UK.
Int J Chron Obstruct Pulmon Dis. 2019 Dec 2;14:2733-2744. doi: 10.2147/COPD.S221852. eCollection 2019.
The RESTORE study, a multi-national randomized, placebo-controlled study, showed that erdosteine - a muco-active antioxidant that modulates bacterial adhesiveness - reduced the rate and duration of exacerbations in moderate and severe COPD with a history of exacerbations. How much benefit patients with less severe disease experience when taking this drug remains unclear.
This post hoc analysis of the 254 RESTORE participants with spirometrically-defined moderate COPD (post-bronchodilator forced expiratory volume in 1 second [FEV] 50‒79% predicted) examined exacerbation rate and duration, time to first exacerbation, and exacerbation-free time. Data were analyzed using descriptive statistics and comparisons between treatment groups used Wilcoxon rank-sum tests, Mann-Whitney -tests, or log rank tests.
Patients with moderate COPD received erdosteine 300 mg twice daily (n=126) or placebo (n=128) added to usual COPD therapy for 12 months. During this time, there were 53 exacerbations in the erdosteine group and 74 in the placebo group, with 42.1% and 57.8% of patients, respectively, experiencing an exacerbation. There was a 47% reduction in the mean exacerbation rate with erdosteine compared to placebo (0.27 vs 0.51 exacerbations per-patient per-year, respectively, =0.003), and a 58.3% reduction in the mild exacerbation rate (0.23 vs 0.53 mild exacerbations per-patient per-year, =0.001). Mean duration of exacerbations was 26% shorter in erdosteine-treated patients (9.1 vs 12.3 days for placebo, =0.022), with significant reductions in the duration of mild and moderate-to-severe exacerbations. Mean time to first exacerbation was prolonged by 7.7% (182 days for erdosteine vs 169 days for placebo, <0.001) and the mean exacerbation-free time was increased by 51 days (279 days for erdosteine vs 228 days for placebo; <0.001).
These results indicate that adding erdosteine to usual COPD maintenance therapy reduces the number of mild, and duration of all, exacerbations in patients with moderate COPD and a history of exacerbations.
RESTORE研究是一项多国随机、安慰剂对照研究,结果显示厄多司坦(一种可调节细菌黏附性的黏液活性抗氧化剂)可降低有加重病史的中重度慢性阻塞性肺疾病(COPD)患者的加重率及加重持续时间。病情较轻的患者服用此药能获得多少益处尚不清楚。
本研究对RESTORE研究中254名经肺量计测定为中度COPD(支气管扩张剂后1秒用力呼气容积[FEV₁]为预测值的50%-79%)的参与者进行事后分析,考察加重率、加重持续时间、首次加重时间及无加重时间。采用描述性统计分析数据,治疗组间比较采用Wilcoxon秩和检验、Mann-Whitney检验或对数秩检验。
中度COPD患者在接受常规COPD治疗的基础上,每日两次服用300mg厄多司坦(n = 126)或安慰剂(n = 128),为期12个月。在此期间,厄多司坦组发生53次加重,安慰剂组发生74次加重,分别有42.1%和57.8%的患者出现加重。与安慰剂相比,厄多司坦使平均加重率降低47%(分别为每人每年0.27次加重和0.51次加重,P = 0.003),轻度加重率降低58.3%(分别为每人每年0.23次轻度加重和0.53次轻度加重,P = 0.001)。厄多司坦治疗的患者加重的平均持续时间缩短26%(安慰剂组为12.3天,厄多司坦组为9.1天,P = 0.022),轻度和中重度加重的持续时间均显著缩短。首次加重的平均时间延长7.7%(厄多司坦组为182天,安慰剂组为169天,P < 0.001),无加重的平均时间增加51天(厄多司坦组为279天,安慰剂组为228天;P < 0.001)。
这些结果表明,在常规COPD维持治疗中加用厄多司坦可减少中度COPD且有加重病史患者的轻度加重次数及所有加重的持续时间。