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支气管扩张症患者接受ARD-3150(吸入性脂质体环丙沙星)48周治疗期间呼吸道症状的变化:ORBIT-3和-4研究结果

Changes in respiratory symptoms during 48-week treatment with ARD-3150 (inhaled liposomal ciprofloxacin) in bronchiectasis: results from the ORBIT-3 and -4 studies.

作者信息

Chalmers James D, Cipolla David, Thompson Bruce, Davis Angela M, O'Donnell Anne, Tino Gregory, Gonda Igor, Haworth Charles, Froehlich Juergen

机构信息

University of Dundee, Dundee, UK

Insmed Incorporated, Bridgewater, NJ, USA.

出版信息

Eur Respir J. 2020 Oct 22;56(4). doi: 10.1183/13993003.00110-2020. Print 2020 Oct.

Abstract

It is not known if inhaled antibiotics improve respiratory symptoms in patients with bronchiectasis. In the recent phase-3 ORBIT trials, 48 weeks' treatment with ARD-3150 (inhaled liposomal ciprofloxacin) did not significantly improve symptoms using the prespecified method of analysis comparing baseline symptoms to those after 48 weeks, when patients had been off treatment for 28 days. This method of analysis does not take account of possible improvements in symptoms while on active treatment.A analysis of two identical randomised trials of ARD-3150 (ORBIT-3 and -4) administered 28 days on and 28 days off in patients with bronchiectasis and chronic infection. The quality-of-life bronchiectasis respiratory symptom scale (QOL-B-RSS), which has a one-week recall period, was administered every 28 days. We examined whether respiratory symptoms improved during on-treatment periods and the relationship of changes in QOL-B-RSS to changes in bacterial load using a mixed-model repeated measures approach.ARD-3150 treatment resulted in a significant improvement in respiratory symptoms during the on-treatment periods with concordant results between ORBIT-3 (estimate 1.4 points, se 0.49; p=0.004) and ORBIT-4 (estimate 1.1 point, se 0.41; p=0.006). The proportion of patients achieving a symptom improvement above the minimum clinically important difference was higher with ARD-3150 compared with placebo during on-treatment cycles (p=0.024). Changes in respiratory symptoms were correlated with changes in bacterial load in the treatment group (r=-0.89, p<0.0001). Individual estimates for decrements in the QOL-B RSS during exacerbation were -9.4 points (se 0.91) in ORBIT-3 and -10.8 points (0.74) in ORBIT-4 (both p<0.0001).Inhaled ARD-3150 resulted in significant improvements in respiratory symptoms during the on-treatment periods which were lost during off-treatment periods. These results supports the concept that reducing bacterial load can improve respiratory symptoms in patients with bronchiectasis.

摘要

目前尚不清楚吸入性抗生素是否能改善支气管扩张症患者的呼吸道症状。在最近的3期ORBIT试验中,使用预先指定的分析方法,将基线症状与48周后(患者停药28天)的症状进行比较,结果显示,使用ARD - 3150(吸入性脂质体环丙沙星)治疗48周并未显著改善症状。这种分析方法没有考虑到在积极治疗期间症状可能出现的改善情况。

对两项相同的随机试验(ORBIT - 3和 - 4)进行分析,这两项试验对支气管扩张症和慢性感染患者采用ARD - 3150给药,给药28天,停药28天。每28天使用具有一周回忆期的支气管扩张症生活质量呼吸道症状量表(QOL - B - RSS)进行评估。我们使用混合模型重复测量方法,研究了治疗期间呼吸道症状是否改善,以及QOL - B - RSS的变化与细菌载量变化之间的关系。

ARD - 3150治疗在治疗期间使呼吸道症状有显著改善,ORBIT - 3(估计改善1.4分,标准误0.49;p = 0.004)和ORBIT - 4(估计改善1.1分,标准误0.41;p = 0.006)的结果一致。在治疗周期中,与安慰剂相比,ARD - 3150使症状改善超过最小临床重要差异的患者比例更高(p = 0.024)。治疗组中呼吸道症状的变化与细菌载量的变化相关(r = - 0.89,p < 0.0001)。在ORBIT - 3中,发作期间QOL - B RSS的个体估计下降值为 - 9.4分(标准误0.91),在ORBIT - 4中为 - 10.8分(0.74)(两者p < 0.0001)。

吸入ARD - 3150在治疗期间使呼吸道症状有显著改善,但在停药期间这些改善消失。这些结果支持了降低细菌载量可改善支气管扩张症患者呼吸道症状这一观点。

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