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Why small particle fixed dose triple therapy? An excursus from COPD pathology to pharmacological treatment evolution

Although bronchodilators are the cornerstone in chronic obstructive pulmonary disease (COPD) therapy, the treatment with a single-agent bronchodilator may not provide adequate symptoms control in COPD. The combination of drugs with different mechanisms of action may be more effective in inducing bro...

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Autores principales: Braido, Fulvio, Corsico, Angelo G., Paleari, Davide, Piraino, Alessio, Cavalieri, Luca, Scichilone, Nicola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8796083/
https://www.ncbi.nlm.nih.gov/pubmed/35044875
http://dx.doi.org/10.1177/17534666211066063
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author Braido, Fulvio
Corsico, Angelo G.
Paleari, Davide
Piraino, Alessio
Cavalieri, Luca
Scichilone, Nicola
author_facet Braido, Fulvio
Corsico, Angelo G.
Paleari, Davide
Piraino, Alessio
Cavalieri, Luca
Scichilone, Nicola
author_sort Braido, Fulvio
collection PubMed
description Although bronchodilators are the cornerstone in chronic obstructive pulmonary disease (COPD) therapy, the treatment with a single-agent bronchodilator may not provide adequate symptoms control in COPD. The combination of drugs with different mechanisms of action may be more effective in inducing bronchodilation and preventing exacerbations, with a lower risk of side-effects in comparison with the increase of the dose of a single molecule. Several studies comparing the triple therapy with the association of long-acting ß(2) agonist (LABA)/inhaled corticosteroid (ICS) or long-acting muscarinic antagonist (LAMA)/LABA reported improvement of lung function and quality of life. A significant reduction in moderate/severe exacerbations has been observed with a fixed triple combination of beclometasone dipropionate (BDP), formoterol fumarate (FF) and glycopyrronium (G) in a single inhaler. The TRILOGY, TRINITY and TRIBUTE studies have provided confirming evidence for a clinical benefit of triple therapy over ICS/LABA combination treatment, LAMA monotherapy and LABA/LAMA combination, with prevention of exacerbations being a key finding. A pooled post hoc analysis of the published clinical studies involving BDP/FF/G fixed combination demonstrated a reduction in fatal events in patients treated with ICS-containing medications, with a trend of statistical significance [hazard ratio = 0.72, 95% confidence interval (CI) 0.50–1.02, p = 0.066], that becomes significant if we consider reduction in fatal events for non-respiratory reasons (hazard ratio = 0.65, 95% CI 0.43–0.97, p = 0.037). In conclusion, a fixed combination of more drugs in a single inhaler can improve long-term adherence to the therapy, reducing the risk of exacerbations and hospital resources utilization. The twice a day administration may provide a better coverage of night, particularly in COPD patients who are highly symptomatic. The inhaled extrafine formulation that allows drug deposition in both large and small – peripheral – airways, is the value added.
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spelling pubmed-87960832022-01-29 Why small particle fixed dose triple therapy? An excursus from COPD pathology to pharmacological treatment evolution Braido, Fulvio Corsico, Angelo G. Paleari, Davide Piraino, Alessio Cavalieri, Luca Scichilone, Nicola Ther Adv Respir Dis Review Although bronchodilators are the cornerstone in chronic obstructive pulmonary disease (COPD) therapy, the treatment with a single-agent bronchodilator may not provide adequate symptoms control in COPD. The combination of drugs with different mechanisms of action may be more effective in inducing bronchodilation and preventing exacerbations, with a lower risk of side-effects in comparison with the increase of the dose of a single molecule. Several studies comparing the triple therapy with the association of long-acting ß(2) agonist (LABA)/inhaled corticosteroid (ICS) or long-acting muscarinic antagonist (LAMA)/LABA reported improvement of lung function and quality of life. A significant reduction in moderate/severe exacerbations has been observed with a fixed triple combination of beclometasone dipropionate (BDP), formoterol fumarate (FF) and glycopyrronium (G) in a single inhaler. The TRILOGY, TRINITY and TRIBUTE studies have provided confirming evidence for a clinical benefit of triple therapy over ICS/LABA combination treatment, LAMA monotherapy and LABA/LAMA combination, with prevention of exacerbations being a key finding. A pooled post hoc analysis of the published clinical studies involving BDP/FF/G fixed combination demonstrated a reduction in fatal events in patients treated with ICS-containing medications, with a trend of statistical significance [hazard ratio = 0.72, 95% confidence interval (CI) 0.50–1.02, p = 0.066], that becomes significant if we consider reduction in fatal events for non-respiratory reasons (hazard ratio = 0.65, 95% CI 0.43–0.97, p = 0.037). In conclusion, a fixed combination of more drugs in a single inhaler can improve long-term adherence to the therapy, reducing the risk of exacerbations and hospital resources utilization. The twice a day administration may provide a better coverage of night, particularly in COPD patients who are highly symptomatic. The inhaled extrafine formulation that allows drug deposition in both large and small – peripheral – airways, is the value added. SAGE Publications 2022-01-19 /pmc/articles/PMC8796083/ /pubmed/35044875 http://dx.doi.org/10.1177/17534666211066063 Text en © The Author(s), 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Review
Braido, Fulvio
Corsico, Angelo G.
Paleari, Davide
Piraino, Alessio
Cavalieri, Luca
Scichilone, Nicola
Why small particle fixed dose triple therapy? An excursus from COPD pathology to pharmacological treatment evolution
title Why small particle fixed dose triple therapy? An excursus from COPD pathology to pharmacological treatment evolution
title_full Why small particle fixed dose triple therapy? An excursus from COPD pathology to pharmacological treatment evolution
title_fullStr Why small particle fixed dose triple therapy? An excursus from COPD pathology to pharmacological treatment evolution
title_full_unstemmed Why small particle fixed dose triple therapy? An excursus from COPD pathology to pharmacological treatment evolution
title_short Why small particle fixed dose triple therapy? An excursus from COPD pathology to pharmacological treatment evolution
title_sort why small particle fixed dose triple therapy? an excursus from copd pathology to pharmacological treatment evolution
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8796083/
https://www.ncbi.nlm.nih.gov/pubmed/35044875
http://dx.doi.org/10.1177/17534666211066063
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