Department of Family and Community Medicine, Faculty of Medicine, University of Toronto, Toronto, ON 12354, Canada.
Medicines Evaluation Unit, Manchester University NHS Foundations Trust, Manchester, UK.
Ther Adv Respir Dis. 2019 Jan-Dec;13:1753466619850725. doi: 10.1177/1753466619850725.
Aclidinium bromide/formoterol fumarate (AB/FF) 400/12 µg is a twice-daily long-acting muscarinic receptor antagonist and long-acting β agonist (LAMA/LABA) dual-bronchodilator maintenance therapy used to relieve symptoms and reduce future risk of exacerbations in adults with chronic obstructive pulmonary disease (COPD). To date, there have been several clinical studies and post hoc analyses of AB/FF, assessing treatment outcomes in patients with moderate-to-severe COPD. These studies have looked at a range of outcomes, including lung function parameters, patient-reported symptom scores, quality-of-life measures assessing impaired health and perceived well-being, and the frequency, duration, and severity of exacerbations. In light of the major 2017 revision to the Global initiative for chronic Obstructive Lung Disease (GOLD) recommendations, and the subsequent updates, we present an update on the latest evidence supporting the efficacy and safety of AB/FF. This review discusses the clinical relevance of the improvements in lung function, symptoms, quality of life, and exacerbations in patients with COPD reported in the phase III and IV trials of AB/FF. Given the current concerns over unnecessary inhaled corticosteroid (ICS) use in COPD, we also touch briefly on the use of blood eosinophils as a biomarker for identifying those patients with COPD already using LAMA/LABA therapy for whom the addition of ICS might be of benefit.
阿地溴铵/富马酸福莫特罗(AB/FF)400/12μg 是一种每日两次的长效毒蕈碱受体拮抗剂和长效β激动剂(LAMA/LABA)双重支气管扩张维持治疗药物,用于缓解症状和降低慢性阻塞性肺疾病(COPD)成人未来加重的风险。迄今为止,已有多项关于 AB/FF 的临床研究和事后分析,评估了中重度 COPD 患者的治疗结局。这些研究着眼于一系列结局,包括肺功能参数、患者报告的症状评分、评估受损健康和感知幸福感的生活质量措施,以及加重的频率、持续时间和严重程度。鉴于全球倡议慢性阻塞性肺疾病(GOLD)建议的 2017 年重大修订版,以及随后的更新,我们提供了最新证据支持 AB/FF 疗效和安全性的更新。这篇综述讨论了在 AB/FF 的 III 期和 IV 期试验中报告的 COPD 患者肺功能、症状、生活质量和加重改善的临床相关性。鉴于目前对 COPD 中不必要使用吸入性皮质类固醇(ICS)的担忧,我们还简要讨论了血液嗜酸性粒细胞作为一种生物标志物的作用,用于识别那些已经使用 LAMA/LABA 治疗的 COPD 患者,对于这些患者,添加 ICS 可能会带来益处。