Division of Pulmonology, Department of Medicine, University of Cape Town, Cape Town, South Africa.
Takeda Pharmaceuticals International GmbH, Zurich, Switzerland.
J Allergy Clin Immunol. 2016 Jul;138(1):142-149.e8. doi: 10.1016/j.jaci.2015.11.035. Epub 2016 Feb 23.
Roflumilast, a selective phosphodiesterase 4 inhibitor, has been shown to provide modest improvements in lung function in patients with mild-to-moderate asthma, but its efficacy in patients with moderate-to-severe asthma has not been assessed. We hypothesized that this drug might provide benefit if combined with montelukast, a leukotriene receptor antagonist, in patients whose symptoms are uncontrolled by inhaled corticosteroids and long-acting β-agonists.
We sought to examine the efficacy, safety, and mode of action of the addition of roflumilast and montelukast versus montelukast alone in patients with moderate-to-severe asthma.
In a phase 2, randomized, double-blind, placebo-controlled, multiple-dose, 2-sequence, crossover study, 64 patients were randomized to receive 500 μg of roflumilast plus montelukast followed by placebo plus 10 mg of montelukast (sequence AB) or placebo plus 10 mg of montelukast followed by 500 μg of roflumilast plus 10 mg of montelukast (sequence BA). All patients had a diagnosis of bronchial asthma inadequately controlled by at least a medium-dose inhaled corticosteroid plus a long-acting β-agonist.
The analysis of FEV1 change from baseline to week 4 showed a statistically significant and clinically meaningful treatment difference of 100 mL for roflumilast plus montelukast versus placebo plus montelukast. Also, improvements in patient-reported outcomes and a reduction in urinary leukotriene E4 levels were observed during roflumilast plus montelukast treatment compared with placebo plus montelukast treatment. Adverse events were consistent with the known safety profile of roflumilast.
The combination of roflumilast with montelukast compared with montelukast alone improved lung function and asthma control in patients with moderate-to-severe asthma and deserves further study for this indication.
罗氟司特是一种选择性磷酸二酯酶 4 抑制剂,已被证明可在轻度至中度哮喘患者中改善肺功能,但尚未评估其在中重度哮喘患者中的疗效。我们假设,如果将其与孟鲁司特联合使用,对于那些吸入性皮质类固醇和长效β激动剂控制症状不佳的患者,该药可能会带来益处。
我们旨在研究罗氟司特和孟鲁司特联合治疗与单独使用孟鲁司特相比,对中重度哮喘患者的疗效、安全性和作用模式。
在一项 2 期、随机、双盲、安慰剂对照、多剂量、2 序列、交叉研究中,64 名患者被随机分为罗氟司特加孟鲁司特组(500μg 罗氟司特加 10mg 孟鲁司特)和安慰剂加孟鲁司特组(10mg 孟鲁司特)(AB 序列)或罗氟司特加孟鲁司特组(500μg 罗氟司特加 10mg 孟鲁司特)和安慰剂加孟鲁司特组(10mg 孟鲁司特)(BA 序列)。所有患者均被诊断为支气管哮喘,吸入性皮质类固醇剂量至少中等,且加用长效β激动剂后仍控制不佳。
从基线到第 4 周的 FEV1 变化分析显示,罗氟司特加孟鲁司特组与安慰剂加孟鲁司特组相比,治疗差异具有统计学意义和临床意义,为 100ml。此外,与安慰剂加孟鲁司特组相比,罗氟司特加孟鲁司特组治疗期间患者报告的结局改善和尿白三烯 E4 水平降低。不良事件与罗氟司特已知的安全性特征一致。
与单独使用孟鲁司特相比,罗氟司特加孟鲁司特联合治疗可改善中重度哮喘患者的肺功能和哮喘控制,这一结果值得进一步研究。