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氟替卡松/福莫特罗与布地奈德/福莫特罗 pMDI 治疗中重度持续性哮喘成人患者的比较:一项为期 12 周的随机对照试验结果。

Comparison of fluticasone/formoterol with budesonide/formoterol pMDI in adults with moderate to severe persistent asthma: Results from a 12-week randomized controlled trial.

机构信息

Chest Care Hospital, Sakkardara Square, Umred Road, Nagpur, India.

Dr. Balamurugan's Chest Clinic, No.2, 1st Cross Street, Janaki Nagar Extn., Valasaravakkam, Chennai, 600 087, India.

出版信息

Pulm Pharmacol Ther. 2018 Feb;48:28-36. doi: 10.1016/j.pupt.2017.09.001. Epub 2017 Sep 8.

Abstract

BACKGROUND

Combination therapy of inhaled corticosteroid/long acting β-agonist (ICS/LABA) is the cornerstone of managing asthmatics who are uncontrolled with low-medium dose of ICS. The novel ICS/LABA combination of fluticasone propionate and formoterol (flu/form) provides potent anti-inflammatory and rapid bronchodilatory effect. This randomized, multi-centre, double-blind study compared the efficacy and safety of flu/form (125/6 mcg BD; Maxiflo) with the well-established budesonide/formoterol combination (bud/form 200/6 mcg BD), both delivered through a pressurized metered dose inhaler (pMDI) in patients with moderate to severe persistent asthma over 12 weeks.

METHODS

This study enrolled patients between 18 and 65 years. The primary end-point was to demonstrate non-inferiority for the mean change in the pre-dose morning peak expiratory flow values (PEF). The secondary end-points included lung function assessments, number of symptom-free days and nights, rescue medication use, day-and night-time symptom scores and safety evaluation.

RESULTS

Two hundred and thirty-two patients were randomized to either flu/form (n = 117) or bud/form (n = 115). At the end of 12 weeks, flu/form was non-inferior to bud/form with regards to the primary end-point of morning PEF (48.07 L/min vs. 49.03 L/min, p > 0.05). These improvements were statistically significant (p < 0.0001) vs baseline. Similar improvements were observed between the two groups for secondary efficacy end-points including FEV, symptom-free nights, rescue medication use, day-and night-time symptom scores (p > 0.05). Flu/form exhibited a safety profile comparable to that of bud/form.

CONCLUSION

Fluticasone/formoterol combination administered through a pMDI is as efficacious and well-tolerated as budesonide/formoterol and offers a new therapeutic option for patients with moderate to severe persistent asthma.

摘要

背景

吸入皮质激素/长效β-激动剂(ICS/LABA)联合治疗是管理对低、中剂量 ICS 控制不佳的哮喘患者的基石。丙酸氟替卡松/福莫特罗(氟/福)这一新型 ICS/LABA 联合制剂具有强大的抗炎和快速支气管扩张作用。这项随机、多中心、双盲研究比较了氟/福(125/6 mcg,每日 2 次;Maxiflo)与已确立的布地奈德/福莫特罗联合制剂(布/福 200/6 mcg,每日 2 次)在 12 周内对中重度持续性哮喘患者的疗效和安全性。

方法

这项研究纳入了 18 至 65 岁的患者。主要终点是证明在给药前清晨呼气峰流量(PEF)的平均变化方面,氟/福不劣于布/福。次要终点包括肺功能评估、无症状天数和夜晚数、急救药物使用、白天和夜间症状评分以及安全性评估。

结果

232 名患者被随机分配至氟/福组(n=117)或布/福组(n=115)。在 12 周结束时,氟/福在清晨 PEF 的主要终点方面不劣于布/福(48.07 L/min 对 49.03 L/min,p>0.05)。这些改善与基线相比具有统计学意义(p<0.0001)。两组的次要疗效终点,包括 FEV1、无症状夜晚数、急救药物使用、白天和夜间症状评分,也观察到类似的改善(p>0.05)。氟/福的安全性与布/福相当。

结论

通过压力定量气雾剂(pMDI)给予氟替卡松/福莫特罗联合治疗与布地奈德/福莫特罗同样有效且耐受良好,为中重度持续性哮喘患者提供了一种新的治疗选择。

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