Triple therapy vs dual inhaler therapy for moderate-to-severe asthma: An updated systematic review and meta-analysis
- PMID: 40516649
- DOI: 10.1016/j.anai.2025.06.011
Triple therapy vs dual inhaler therapy for moderate-to-severe asthma: An updated systematic review and meta-analysis
Abstract
Background: Long-acting muscarinic antagonists are typically added to inhaled corticosteroids (ICS) and long-acting β-agonists (LABA) for asthma management.
Objective: To systematically synthesize the benefits and harms of triple therapy (ICS/LABA/long-acting muscarinic antagonists) compared with dual therapy (ICS/LABA) for asthma management across key subpopulations as part of developing linked American Academy of Allergy, Asthma, and Immunology/American College of Allergy, Asthma, and Immunology guidelines.
Methods: We searched MEDLINE, EMBASE, the Cochrane Controlled Register of Trials, and the International Clinical Trials Registry Platform from January 1, 2020 to February 1, 2025, for randomized trials comparing inhaled triple therapy to dual therapy for asthma to update our previous systematic review. Paired reviewers independently screened citations, extracted data, and assessed the risk of bias. Random effects meta-analyses assessed asthma control (asthma control questionnaire-7; 0-6), asthma-related quality of life (asthma quality of life questionnaire; 1-7), prebronchodilator forced expiratory volume in 1 second, severe exacerbations, and serious adverse events. The Grading of Recommendations, Assessment, Development, and Evaluation approach informed the certainty of evidence. Open Science Framework Registration (https://osf.io/u8t4q/).
Results: A total of 26 trials randomized 12,431 participants. Compared with dual therapy, triple therapy reduces severe exacerbations in patients at high risk for future exacerbation (relative risk 0.83, 95% CI 0.76-0.90; risk difference 5.3% fewer; high certainty), with trivial improvement in asthma control (mean difference [MD] -0.04, 95% CI -0.07 to 0.00, moderate certainty; lower better), quality of life (MD 0.05, 95% CI -0.03 to 0.14, moderate certainty; higher better), and prebronchodilator forced expiratory volume in 1 second (MD 0.07, 95% CI 0.05-0.09; high certainty), without increase in serious adverse events (moderate certainty). The effects were consistent across age, body mass index, and exacerbation history.
Conclusion: In patients with moderate-to-severe asthma, triple therapy, compared with dual therapy, reduces severe exacerbations in patients at high risk for future exacerbation with minimal harm.
Copyright © 2025 The Authors. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Disclosures Dr Hoyte reports receiving consulting, advisory board, and/or speaking fees from AstraZeneca and GlaxoSmithKline (GSK). Dr Sumino reports receiving consulting, advisory board, and/or speaking fees from Teva and Kyorin Pharmaceutical. Dr Israel reports receiving personal fees from Amgen, Arrowhead Pharmaceuticals, AstraZeneca, GSK, Merck, Regeneron, Sanofi, Teva, Apogee Therapeutics, Yuhan, Leerink Partners, Jasper Therapeutics, Generate:Biomedicines, and UpToDate; nonfinancial support from Genentech, Sun Pharma, Laurel Pharmaceuticals, Om Pharma, Nestlé, CSL Behring, and Sanofi-Regeneron; and research grants from Genentech, Amgen, GSK, AstraZeneca, Avillion, Gossamer Bio, National Institutes of Health, and Patient-Centered Outcomes Research Institute. Dr O’Byrne reports receiving consulting, advisory board, and/or speaking fees and research grants from AstraZeneca and GSK. Dr Bacharier reports receiving consulting, advisory board, and/or speaking fees with AstraZeneca and Novartis. Dr Mosnaim reports receiving research grants from Areteia Therapeutics, GSK, Genentech, Incyte, Novartis, Sanofi-Regeneron, and Teva; and consulting, advisory board, and/or speaking fees from Jasper Therapeutics, Aptar, Chiesi, Genentech, Novartis, Sanofi-Regeneron, and Teva. The remaining authors have no conflicts of interest to report.
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