EVELUT®: a real-world, observational study assessing dyspnoea and symptom burden in COPD patients switched from LABA/ICS to LAMA/LABA or LAMA/LABA/ICS

dc.contributor.authorBuhl, Roland
dc.contributor.authorDreher, Michael
dc.contributor.authorMattiucci-Guehlke, Muriel
dc.contributor.authorEmerson-Stadler, Rachel
dc.contributor.authorEckhardt, Sebastian
dc.contributor.authorTaube, Christian
dc.contributor.authorVogelmeier, Claus F.
dc.date.accessioned2023-08-24T07:23:38Z
dc.date.available2023-08-24T07:23:38Z
dc.date.issued2023
dc.description.abstractIntroduction The Global Initiative for Chronic Obstructive Lung Disease (GOLD 2023) no longer recommends a long-acting β2-agonist (LABA) plus inhaled corticosteroid (ICS) combination for the treatment of chronic obstructive pulmonary disease (COPD). In patients treated with LABA/ICS, who continue to experience symptoms without frequent or severe exacerbations, GOLD now recommends switching to long-acting muscarinic antagonist (LAMA)/LABA instead of escalating to triple therapy (TT; LAMA/LABA/ICS), which previously was also a recommended option. EVELUT®, a real-life, observational study, compared these two treatment strategies in terms of symptom relief and health status improvement. Methods Patients with symptomatic COPD at low exacerbation risk (GOLD B) were switched, at their physicians’ discretion, from LABA/ICS to either fixed-dose LAMA/LABA (tiotropium/olodaterol, Respimat® [Tio/Olo]) or fixed or free TT. Primary endpoints were change in modified Medical Research Council (mMRC) and COPD Assessment Test™ (CAT™) scores after 12 weeks. Results The safety set contained 463 patients (Tio/Olo, n = 329; TT, n = 134). In a propensity score-matched set (Tio/Olo, n = 121; TT, n = 121), improvement in mMRC score was similar in patients on Tio/Olo (–0.23; 95% confidence interval [CI] –0.11, –0.36) and TT (–0.25; 95% CI –0.13, –0.38). Improvement in total CAT score was slightly larger in patients on Tio/Olo (–3.45; 95% CI –2.45, –4.45) versus TT (–2.51; 95% CI –1.62, –3.40). In both groups, Physician’s Global Evaluation scores increased, with 69–89% of patients satisfied with their treatment overall. Marginally more patients on Tio/Olo responded to treatment versus TT (Δ mMRC score ≥ 1; 25% vs. 22%; Δ CAT score ≥ 2, 68% vs. 56%). Conclusion In patients with symptomatic COPD at low exacerbation risk, treatment can be switched from LABA/ICS to LAMA/LABA without compromising clinical benefit, compared with escalating to LAMA/LABA/ICS. Switching from LABA/ICS to LAMA/LABA can provide symptom relief and improve health status without exposure to the risks associated with ICS.en_GB
dc.identifier.doihttp://doi.org/10.25358/openscience-9468
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/9486
dc.language.isoeng
dc.rightsCC-BY-NC-4.0
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleEVELUT®: a real-world, observational study assessing dyspnoea and symptom burden in COPD patients switched from LABA/ICS to LAMA/LABA or LAMA/LABA/ICSen_GB
dc.typeZeitschriftenaufsatzde_DE
jgu.apc.pricePAR-Fee
jgu.apc.transformationcontractSpringer (DEAL)
jgu.journal.titleAdvances in therapy
jgu.journal.volume40
jgu.organisation.departmentFB 04 Medizinde_DE
jgu.organisation.nameJohannes Gutenberg-Universität Mainzde_DE
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.end3278
jgu.pages.start3263
jgu.publisher.doi10.1007/s12325-023-02524-y
jgu.publisher.issn1865-8652
jgu.publisher.nameSpringer Healthcare Communications
jgu.publisher.placeTarporley
jgu.publisher.year2023
jgu.rights.accessrightsopenAccessen_GB
jgu.subject.ddccode610
jgu.subject.dfgLebenswissenschaftende_DE
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTexten_GB
jgu.type.versionPublished versionen_GB

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