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Benefit/Risk Profile of Single-Inhaler Triple Therapy in COPD.

Bourbeau, J; Bafadhel, M; Barnes, NC; Compton, C; Di Boscio, V; Lipson, DA; Jones, PW; Martin, N; Weiss, G; Halpin, DMG (2021) Benefit/Risk Profile of Single-Inhaler Triple Therapy in COPD. Int J Chron Obstruct Pulmon Dis, 16. pp. 499-517. ISSN 1178-2005 https://doi.org/10.2147/COPD.S291967
SGUL Authors: Jones, Paul Wyatt

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Abstract

Chronic obstructive pulmonary disease (COPD) is associated with major healthcare and socioeconomic burdens. International consortia recommend a personalized approach to treatment and management that aims to reduce both symptom burden and the risk of exacerbations. Recent clinical trials have investigated single-inhaler triple therapy (SITT) with a long-acting muscarinic antagonist (LAMA), long-acting β2-agonist (LABA), and inhaled corticosteroid (ICS) for patients with symptomatic COPD. Here, we review evidence from randomized controlled trials showing the benefits of SITT and weigh these against the reported risk of pneumonia with ICS use. We highlight the challenges associated with cross-trial comparisons of benefit/risk, discuss blood eosinophils as a marker of ICS responsiveness, and summarize current treatment recommendations and the position of SITT in the management of COPD, including potential advantages in terms of improving patient adherence. Evidence from trials of SITT versus dual therapies in symptomatic patients with moderate to very severe airflow limitation and increased risk of exacerbations shows benefits in lung function and patient-reported outcomes. Moreover, the key benefits reported with SITT are significant reductions in exacerbations and hospitalizations, with data also suggesting reduced all-cause mortality. These benefits outweigh the ICS-class effect of higher incidence of study-reported pneumonia compared with LAMA/LABA. Important differences in trial design, baseline population characteristics, such as exacerbation history, and assessment of outcomes, have significant implications for interpreting data from cross-trial comparisons. Current understanding interprets the blood eosinophil count as a continuum that can help predict response to ICS and has utility alongside other clinical factors to aid treatment decision-making. We conclude that treatment decisions in COPD should be guided by an approach that considers benefit versus risk, with early optimization of treatment essential for maximizing long-term benefits and patient outcomes.

Item Type: Article
Additional Information: © 2021 Bourbeau et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/ terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php)
Keywords: ICS, LABA, LAMA, all-cause mortality, exacerbations, hospitalizations, 1102 Cardiorespiratory Medicine and Haematology, Respiratory System
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Int J Chron Obstruct Pulmon Dis
ISSN: 1178-2005
Language: eng
Dates:
DateEvent
1 March 2021Published
7 February 2021Accepted
Publisher License: Creative Commons: Attribution-Noncommercial 3.0
PubMed ID: 33688176
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/113080
Publisher's version: https://doi.org/10.2147/COPD.S291967

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