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