Department of Pulmonology, Celal Bayar University, Manisa, Turkey.
ProAR and Universidade Federal da Bahia, Salvador, Brazil.
Respir Med. 2023 Nov;218:107377. doi: 10.1016/j.rmed.2023.107377. Epub 2023 Jul 29.
Current treatment for moderate-severe asthma with inhaled corticosteroid (ICS)-based therapy can follow two strategies: a single inhaler maintenance and reliever therapy (MART) regimen, or regular dosing with ICS/long-acting β-agonist used as maintenance therapy plus a separate short acting β-agonist reliever inhaler. It would be clinically useful to understand the potential of patient traits to influence regular dosing or MART treatment outcomes.
A systematic literature review (SLR) and meta-analysis was conducted to identify specific patient traits that may predict improved clinical outcomes with regular dosing or MART.
The SLR identified 28 studies in patients with moderate-severe asthma assessing regular dosing or MART treatments and reporting the traits and outcomes of interest. Network meta-regressions found no significant difference in the relative efficacy of regular dosing as compared with MART on any of the clinical outcomes (exacerbation rate, time to first exacerbation, FEV, reliever use and adherence) for any of the patient traits (baseline lung function, baseline ACQ, age, BMI, and smoking history) evaluated. However, some trends towards traits influencing treatment efficacy were identified. Inconsistent reporting of traits and outcomes was observed between trials.
The analysed patient traits evaluated in this study were associated with similar efficacy for the analysed outcomes to either regular dosing or MART; however, trends from the data observed encourage future analyses for possible identification of additional traits, or a combination of traits, that may be of interest. More comparable reporting of clinically important traits and outcomes would improve future analyses.
对于采用吸入性皮质类固醇(ICS)为基础疗法的中重度哮喘,目前的治疗可遵循两种策略:一种是单一吸入器维持和缓解治疗(MART)方案,或是采用 ICS/长效β激动剂作为维持疗法的常规剂量,再加上单独的短效β激动剂缓解吸入器。了解患者特征对常规剂量或 MART 治疗结果的潜在影响将具有临床意义。
进行了系统文献回顾(SLR)和荟萃分析,以确定可能预测常规剂量或 MART 治疗改善临床结局的特定患者特征。
SLR 确定了 28 项评估中重度哮喘患者常规剂量或 MART 治疗并报告相关特征和结局的研究。网络荟萃回归分析发现,对于任何评估的患者特征(基线肺功能、基线 ACQ、年龄、BMI 和吸烟史),常规剂量与 MART 相比,在任何临床结局(加重率、首次加重时间、FEV、缓解药物使用和依从性)上的相对疗效均无显著差异。然而,观察到一些特征影响治疗效果的趋势。试验之间对特征和结局的报告不一致。
本研究评估的患者特征与常规剂量或 MART 分析结局的疗效相似;然而,从观察到的数据中得出的趋势鼓励未来进行可能的其他特征或特征组合的分析,这些特征可能具有研究意义。更可比地报告临床重要特征和结局将改善未来的分析。