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Single-inhaler triple therapy in symptomatic COPD patients: FULFIL subgroup analyses

机译:有症状COPD患者的单吸入三联疗法:FULFILL亚组分析

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Triple inhaled corticosteroid (ICS)/long-acting muscarinic antagonist (LAMA)/long-acting β2-agonist (LABA) therapy is recommended for symptomatic patients with chronic obstructive pulmonary disease (COPD) and at risk of exacerbations. However, the benefits versus side-effects of triple inhaled therapy for COPD, based on distinct patient clinical profiles, are unclear.FULFIL, a phase III, randomised, double-blind study, compared 24 weeks of once-daily fluticasone furoate/umeclidinium/vilanterol (FF/UMEC/VI) 100/62.5/25 µg using the Ellipta inhaler with twice-daily budesonide/formoterol (BUD/FOR) 400/12 µg using the Turbuhaler. Subgroup analyses of forced expiratory volume in 1 s (FEV1), St George's Respiratory Questionnaire (SGRQ) Total score and exacerbation rates were carried out. Subgroups were defined by COPD medication at screening (ICS+LABA, BUD+FOR, ICS+LABA+LAMA, LAMA alone, tiotropium alone and LAMA+LABA), by disease severity (lung function and exacerbations) and by exacerbation history (exacerbation severity and frequency).In the intent-to-treat population (n=1810) at week 24, FF/UMEC/VI (n=911) versus BUD/FOR (n=899) improved FEV1 and SGRQ Total score and reduced mean annual exacerbation rates in all disease severity and exacerbation history subgroups. FF/UMEC/VI versus BUD/FOR improved FEV1 and SGRQ Total score in all medication subgroups and reduced mean annual exacerbation rates in all medication subgroups, except LAMA+LABA. Adverse events were similar across subgroups.These findings support the benefit of FF/UMEC/VI compared with dual ICS/LABA therapy in patients with symptomatic COPD regardless of disease severity or prior treatment and may help to inform clinical decision making.
机译:对于患有慢性阻塞性肺疾病(COPD)并有加重病情的有症状患者,建议三重吸入皮质类固醇(ICS)/长效毒蕈碱拮抗剂(LAMA)/长效β2-激动剂(LABA)治疗。然而,根据不同的患者临床情况,三次吸入疗法对COPD的益处与副作用尚不清楚.FULFIL是一项III期随机,双盲研究,比较了每天一次氟替卡松糠酸酯/ umeclidinium / 24周治疗使用Ellipta吸入器的维兰特罗(FF / UMEC / VI)为100 / 62.5 /25μg,每天两次使用布地奈德/福莫特罗(BUD / FOR)的Turbuhaler为400 /12μg。进行了以1秒为单位的强迫呼气量(FEV1),圣乔治呼吸问卷(SGRQ)的亚组分析。通过筛选时的COPD药物(ICS + LABA,BUD + FOR,ICS + LABA + LAMA,单独的LAMA,单独的噻托溴铵和LAMA + LABA),疾病的严重程度(肺功能和急性加重)和恶化的病史(恶化的严重程度)来定义亚组。在第24周的意向性治疗人群(n = 1810)中,FF / UMEC / VI(n = 911)与BUD / FOR(n = 899)改善了FEV1和SGRQ总分并降低了年均所有疾病严重程度和恶化史亚组的恶化率。 FF / UMEC / VI与BUD / FOR相比,所有药物亚组的FEV1和SGRQ总分得到改善,除LAMA + LABA外,所有药物亚组的年平均恶化率均降低。各亚组的不良事件相似。这些发现支持FF / UMEC / VI与有症状COPD患者的双重ICS / LABA治疗相比,无论疾病的严重程度或先前的治疗如何,均可能有助于临床决策。

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