Reynolds Neil A, Perry Caroline M, Keating Gillian M
Adis International Limited, Auckland, New Zealand.
Drugs. 2004;64(4):431-41; discussion 433-4. doi: 10.2165/00003495-200464040-00006.
Budesonide/formoterol is a fixed-dose combination of the corticosteroid budesonide and the long-acting beta2-agonist formoterol, and is inhaled via the Turbuhaler device. In two large, randomised, double-blind, 12-month studies, patients with severe chronic obstructive pulmonary disease (COPD) receiving budesonide/formoterol 320/9 microg twice daily had a significantly higher forced expiratory volume in 1 second (FEV1) and significantly higher morning and evening peak expiratory flow at trial endpoint than recipients of budesonide or placebo; FEV1 was significantly higher than with formoterol in the larger study. In both studies, the rate of COPD exacerbations and exacerbations requiring oral corticosteroids was significantly reduced with budesonide/formoterol versus formoterol and placebo. Moreover, the time to first exacerbation was significantly prolonged with budesonide/formoterol versus all other treatment arms in the larger study. At 12 months, significant improvements in health-related quality-of-life scores were seen with budesonide/formoterol versus placebo in both studies. The reduction in total and individual symptom scores was significantly greater with budesonide/formoterol than with budesonide or placebo in the smaller study. Budesonide/formoterol was generally well tolerated by patients with severe COPD. The tolerability profile of the combination was similar to that of the individual components with no increase in the incidence of adverse events.
布地奈德/福莫特罗是皮质类固醇布地奈德与长效β2受体激动剂福莫特罗的固定剂量组合,通过都保装置吸入。在两项大型、随机、双盲、为期12个月的研究中,重度慢性阻塞性肺疾病(COPD)患者每日两次吸入320/9微克布地奈德/福莫特罗,在试验终点时,其1秒用力呼气容积(FEV1)显著更高,早晚呼气峰值流速也显著更高,高于接受布地奈德或安慰剂的患者;在规模较大的研究中,FEV1显著高于使用福莫特罗的患者。在两项研究中,与福莫特罗和安慰剂相比,布地奈德/福莫特罗显著降低了COPD急性加重的发生率以及需要口服皮质类固醇治疗的急性加重发生率。此外,在规模较大的研究中,与所有其他治疗组相比,布地奈德/福莫特罗使首次急性加重的时间显著延长。在12个月时,两项研究中布地奈德/福莫特罗组与安慰剂组相比,健康相关生活质量评分均有显著改善。在规模较小的研究中,布地奈德/福莫特罗使总症状评分和个体症状评分的降低幅度显著大于布地奈德或安慰剂。重度COPD患者对布地奈德/福莫特罗总体耐受性良好。该组合的耐受性与各单一成分相似,不良事件发生率未增加。