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Comparing major COPD triple therapy trials using a structured multi-criteria decision analysis: A deep dive into patient populations and outcomes - 01/09/25

Doi : 10.1016/j.rmed.2025.108292 
Mario Cazzola a, , Mauro Maniscalco b, c, Vincenzo Patella d, e, Luigino Calzetta f, Maria Gabriella Matera g, Paola Rogliani a
a Unit of Respiratory Medicine, Department of Experimental Medicine, University of Rome ‘Tor Vergata’, Rome, Italy 
b Pulmonary Rehabilitation Unit of Telese Terme Institute, Istituti Clinici Scientifici Maugeri IRCCS, Telese Terme, 82037, Italy 
c Department of Clinical Medicine and Surgery, University of Naples "Federico II", Naples, 80131, Italy 
d Department of Internal Medicine ASL Salerno, ‘Santa Maria della Speranza’ Hospital, Italy 
e Postgraduate Program in Allergy and Clinical Immunology, University of Naples ‘Federico II’, Naples, Italy 
f Department of Medicine and Surgery, Respiratory Disease and Lung Function Unit, University of Parma, Parma, Italy 
g Unit of Pharmacology, Department of Experimental Medicine, University of Campania ‘Luigi Vanvitelli’, Naples, Italy 

Corresponding author.

Abstract

Background

Triple inhaled therapy (ICS/LABA/LAMA) is widely recommended for managing COPD in patients with persistent symptoms or frequent exacerbations. However, variability in trial designs, populations, and pharmacologic formulations complicates direct comparison between regimens.

Objective

To evaluate the comparative performance of three triple therapies, FF/VI/UMEC, BUD/FOR/GLY, and BDP/FOR/GLY, using a multidimensional comparative decision analysis (MCDA) across key clinical domains.

Methods

Data from pivotal trials (IMPACT, FULFIL, TRINITY, TRIBUTE, TRILOGY, ETHOS, and KRONOS) were synthesized using an MCDA framework encompassing lung function, symptom control, and exacerbations. Mortality, safety, and device usability were also assessed. Analyses considered variations in enrolled populations, prior ICS use, and inhaler characteristics.

Results

FF/VI/UMEC showed consistent efficacy across multiple domains and populations, particularly in patients at high risk of exacerbations. BUD/FOR/GLY was associated with reductions in exacerbations and mortality, particularly in patients previously treated with LABA/LAMA. BDP/FOR/GLY may be suitable for ICS-maintained patients. Trials like FULFIL and KRONOS showed symptom and lung function gains even in non-exacerbators, although ICS use in this group always warrants caution due to pneumonia risk.

Limitations

Findings are based on indirect comparisons across heterogeneous trials. Relative changes from dual therapy comparators were evaluated, and pharmacological and device-related differences between each triple therapy and the comparators may have influenced outcomes.

Conclusions

Among the therapies evaluated, FF/VI/UMEC achieved the highest composite MCDA score. However, optimal COPD management requires personalized treatment to be prescribed based on factors such as exacerbation history, previous ICS use, inhaler preference and adherence. This may involve evaluating the use of an alternative triple therapy and emphasizes the importance of aligning the choice of triple therapy with the individual's clinical profile and treatment goals.

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Highlights

Triple therapy is key for COPD patients with persistent symptoms or frequent exacerbations.
Three triple therapies, FF/VI/UMEC, BUD/FOR/GLY, and BDP/FOR/GLY, have been approved.
The substantial differences in pivotal RCTs make it difficult to compare these therapies.
MCDA offers comparative insights into triple therapies, highlighting their distinct profiles.
Despite limitations, findings provide a basis for selecting the best triple therapy.

Il testo completo di questo articolo è disponibile in PDF.

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© 2025  The Authors. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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