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The 6-min walk test as a primary end-point in interstitial lung disease
There is a need for clinical trial end-points to better assess how patients feel and function, so that interventions can be developed which alleviate symptoms and improve quality of life. Use of 6-min walk test (6MWT) outcomes as a primary end-point in interstitial lung disease (ILD) trials is growi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Respiratory Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9724818/ https://www.ncbi.nlm.nih.gov/pubmed/36002171 http://dx.doi.org/10.1183/16000617.0087-2022 |
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author | Harari, Sergio Wells, Athol U. Wuyts, Wim A. Nathan, Steven D. Kirchgaessler, Klaus-Uwe Bengus, Monica Behr, Jürgen |
author_facet | Harari, Sergio Wells, Athol U. Wuyts, Wim A. Nathan, Steven D. Kirchgaessler, Klaus-Uwe Bengus, Monica Behr, Jürgen |
author_sort | Harari, Sergio |
collection | PubMed |
description | There is a need for clinical trial end-points to better assess how patients feel and function, so that interventions can be developed which alleviate symptoms and improve quality of life. Use of 6-min walk test (6MWT) outcomes as a primary end-point in interstitial lung disease (ILD) trials is growing, particularly for drugs targeting concurrent pulmonary hypertension. However, 6MWT outcomes may be influenced differentially by interstitial lung and pulmonary vascular components of ILD, making interpretation complicated. We propose that using 6MWT outcomes, including 6-min walk distance or oxygen desaturation, as primary end-points should depend upon the study population (how advanced the ILD is; whether vasculopathy is significant), the degree of disease progression, and, importantly, the effect of study treatment expected. We argue that the 6MWT as a single outcome measure is suitable as a primary end-point if the treatment goal is to improve functional performance or prevent disease progression within a study population of patients with advanced ILD or those with ILD and co-existent vasculopathy. In addition, we discuss the potential of composite primary end-points incorporating 6MWT outcomes, outlining important considerations to ensure that they are appropriate for the study population and treatment goals. |
format | Online Article Text |
id | pubmed-9724818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | European Respiratory Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97248182022-12-08 The 6-min walk test as a primary end-point in interstitial lung disease Harari, Sergio Wells, Athol U. Wuyts, Wim A. Nathan, Steven D. Kirchgaessler, Klaus-Uwe Bengus, Monica Behr, Jürgen Eur Respir Rev Reviews There is a need for clinical trial end-points to better assess how patients feel and function, so that interventions can be developed which alleviate symptoms and improve quality of life. Use of 6-min walk test (6MWT) outcomes as a primary end-point in interstitial lung disease (ILD) trials is growing, particularly for drugs targeting concurrent pulmonary hypertension. However, 6MWT outcomes may be influenced differentially by interstitial lung and pulmonary vascular components of ILD, making interpretation complicated. We propose that using 6MWT outcomes, including 6-min walk distance or oxygen desaturation, as primary end-points should depend upon the study population (how advanced the ILD is; whether vasculopathy is significant), the degree of disease progression, and, importantly, the effect of study treatment expected. We argue that the 6MWT as a single outcome measure is suitable as a primary end-point if the treatment goal is to improve functional performance or prevent disease progression within a study population of patients with advanced ILD or those with ILD and co-existent vasculopathy. In addition, we discuss the potential of composite primary end-points incorporating 6MWT outcomes, outlining important considerations to ensure that they are appropriate for the study population and treatment goals. European Respiratory Society 2022-08-24 /pmc/articles/PMC9724818/ /pubmed/36002171 http://dx.doi.org/10.1183/16000617.0087-2022 Text en Copyright ©The authors 2022 https://creativecommons.org/licenses/by-nc/4.0/This version is distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0. For commercial reproduction rights and permissions contact permissions@ersnet.org (mailto:permissions@ersnet.org) |
spellingShingle | Reviews Harari, Sergio Wells, Athol U. Wuyts, Wim A. Nathan, Steven D. Kirchgaessler, Klaus-Uwe Bengus, Monica Behr, Jürgen The 6-min walk test as a primary end-point in interstitial lung disease |
title | The 6-min walk test as a primary end-point in interstitial lung disease |
title_full | The 6-min walk test as a primary end-point in interstitial lung disease |
title_fullStr | The 6-min walk test as a primary end-point in interstitial lung disease |
title_full_unstemmed | The 6-min walk test as a primary end-point in interstitial lung disease |
title_short | The 6-min walk test as a primary end-point in interstitial lung disease |
title_sort | 6-min walk test as a primary end-point in interstitial lung disease |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9724818/ https://www.ncbi.nlm.nih.gov/pubmed/36002171 http://dx.doi.org/10.1183/16000617.0087-2022 |
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