Sion Katya Y J, Huisman Eline L, Punekar Yogesh S, Naya Ian, Ismaila Afisi S
Real World Strategy and Analytics, Mapi Group, Houten, The Netherlands.
Care and Public Health Research Institute, Maastricht University, Maastricht, The Netherlands.
Pulm Ther. 2017 Dec;3(2):297-316. doi: 10.1007/s41030-017-0048-0. Epub 2017 Aug 22.
Comparative data on the efficacies of long-acting muscarinic antagonist (LAMA) and long-acting β-agonist (LABA) combinations for the treatment of moderate-to-very-severe chronic obstructive pulmonary disease (COPD) are limited. The aim of this Bayesian network meta-analysis (NMA) is to assess the relative efficacies of available open combinations (delivered via separate inhalers) and fixed-dose combinations (FDCs, delivered via a single inhaler).
We conducted a systematic literature review with the aim of identifying randomized controlled trials (RCTs) of ≥8-week duration in adults aged ≥40 years with COPD that compared LAMA + LABA combinations with each other, with tiotropium (TIO), or with placebo. Data on changes from baseline in trough forced expiratory volume in 1 s (FEV) and on St George's Respiratory Questionnaire (SGRQ) total score, the Transition Dyspnea Index (TDI) focal score, and rescue medication use at 12 and 24 weeks were extracted from these RCTs and analyzed using a NMA in a Bayesian framework.
Data from 44 RCTs were included in the NMA. All FDCs showed improvements relative to placebo in terms of trough FEV, SGRQ total score, and TDI focal score above clinically relevant thresholds, with the exception of TIO/olodaterol and aclidinium/formoterol, both of which failed to show clinically relevant improvements in SGRQ score at 24 weeks. All FDCs demonstrated reduced rescue medication use versus placebo. Open combinations demonstrated improved efficacy in all outcomes versus placebo, but these improvements did not consistently exceed clinically relevant thresholds for SGRQ and TDI scores. All once-daily FDCs showed improved efficacy versus TIO, but improvements were less consistently observed versus TIO with open dual combinations and combinations containing formoterol or salmeterol administered twice daily. Relative probabilities of improvement between FDCs highlighted potential between-class differences for trough FEV but suggested little potential for differences in patient-reported outcomes.
LAMA + LABA combinations generally showed improved outcomes versus placebo and TIO. FDCs appeared to perform better than open dual combinations. A potential effectiveness gradient was observed between FDCs for objectively assessed functional outcomes, although further prospective trials are required to confirm these findings.
GSK.
长效毒蕈碱拮抗剂(LAMA)与长效β受体激动剂(LABA)联合用药治疗中度至极重度慢性阻塞性肺疾病(COPD)疗效的对比数据有限。本贝叶斯网络荟萃分析(NMA)旨在评估现有开放联合制剂(通过单独吸入器给药)和固定剂量复方制剂(FDC,通过单一吸入器给药)的相对疗效。
我们进行了一项系统的文献综述,旨在识别年龄≥40岁的COPD成年患者中持续时间≥8周的随机对照试验(RCT),这些试验比较了LAMA + LABA联合制剂相互之间、与噻托溴铵(TIO)或与安慰剂的疗效。从这些RCT中提取1秒用力呼气容积(FEV)谷值相对于基线的变化数据、圣乔治呼吸问卷(SGRQ)总分、过渡性呼吸困难指数(TDI)焦点评分以及12周和24周时急救药物使用情况的数据,并在贝叶斯框架下使用NMA进行分析。
44项RCT的数据纳入了NMA。所有FDC在FEV谷值、SGRQ总分和TDI焦点评分方面相对于安慰剂均有改善,且改善程度高于临床相关阈值,但噻托溴铵/奥达特罗和阿地溴铵/福莫特罗除外,这两种药物在24周时SGRQ评分未显示出临床相关改善。所有FDC与安慰剂相比急救药物使用减少。开放联合制剂相对于安慰剂在所有结局方面均显示疗效改善,但这些改善在SGRQ和TDI评分方面并未始终超过临床相关阈值。所有每日一次的FDC相对于TIO显示疗效改善,但在与TIO比较时,开放双联制剂以及含福莫特罗或沙美特罗的每日两次给药联合制剂的改善情况不太一致。FDC之间改善的相对概率突出了FEV谷值在类别间的潜在差异,但提示患者报告结局方面差异的可能性较小。
LAMA + LABA联合制剂总体上相对于安慰剂和TIO显示出更好的结局。FDC似乎比开放双联制剂表现更好。在客观评估的功能结局方面,FDC之间观察到潜在的有效性梯度,尽管需要进一步的前瞻性试验来证实这些发现。
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