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The relevance of fatigue to relapse rate in multiple sclerosis: Applying patient preference data to the OPTIMUM trial
BACKGROUND: In the OPTIMUM trial in patients with relapsing MS, treatment differences in annualized relapse rate (ARR, 0.088) and change in fatigue at week 108 (3.57 points, measured using the Fatigue Symptoms and Impacts Questionnaire–Relapsing Multiple Sclerosis, symptom domain (FSIQ-RMS-S)) favor...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972232/ https://www.ncbi.nlm.nih.gov/pubmed/36550636 http://dx.doi.org/10.1177/13524585221140270 |
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author | Fox, Robert J Tervonen, Tommi Phillips-Beyer, Andrea Sidorenko, Tatiana Boyanova, Neli Brooks, Anne Hennessy, Brian Jamieson, Carol Levitan, Bennett |
author_facet | Fox, Robert J Tervonen, Tommi Phillips-Beyer, Andrea Sidorenko, Tatiana Boyanova, Neli Brooks, Anne Hennessy, Brian Jamieson, Carol Levitan, Bennett |
author_sort | Fox, Robert J |
collection | PubMed |
description | BACKGROUND: In the OPTIMUM trial in patients with relapsing MS, treatment differences in annualized relapse rate (ARR, 0.088) and change in fatigue at week 108 (3.57 points, measured using the Fatigue Symptoms and Impacts Questionnaire–Relapsing Multiple Sclerosis, symptom domain (FSIQ-RMS-S)) favored ponesimod over teriflunomide. However, the importance of the fatigue outcome to patients was unclear. OBJECTIVE: To assess the importance of the OPTIMUM FSIQ-RMS-S results using data from an MS discrete choice experiment (DCE). METHODS: The DCE included components to correlate levels of physical and cognitive fatigue with FSIQ-RMS-S scores. Changes in relapses/year and time to MS progression equivalent to the treatment difference in fatigue in OPTIMUM were determined for similar fatigue levels as mean baseline fatigue in OPTIMUM. RESULTS: DCE participants would accept 0.06 more relapses/year or a 0.15–0.17 year decrease in time to MS progression for a 3.57-point difference in physical fatigue on the FSIQ-RMS-S. To improve cognitive fatigue by 3.57-points on the FSIQ-RMS-S, DCE participants would accept 0.09–0.10 more relapses/year or a 0.24–0.28 year decrease in time to MS progression. CONCLUSION: MS patients would accept 0.06 more relapses/year to change their fatigue by a similar magnitude as the between-treatment difference observed in the OPTIMUM trial. |
format | Online Article Text |
id | pubmed-9972232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-99722322023-03-01 The relevance of fatigue to relapse rate in multiple sclerosis: Applying patient preference data to the OPTIMUM trial Fox, Robert J Tervonen, Tommi Phillips-Beyer, Andrea Sidorenko, Tatiana Boyanova, Neli Brooks, Anne Hennessy, Brian Jamieson, Carol Levitan, Bennett Mult Scler Original Research Papers BACKGROUND: In the OPTIMUM trial in patients with relapsing MS, treatment differences in annualized relapse rate (ARR, 0.088) and change in fatigue at week 108 (3.57 points, measured using the Fatigue Symptoms and Impacts Questionnaire–Relapsing Multiple Sclerosis, symptom domain (FSIQ-RMS-S)) favored ponesimod over teriflunomide. However, the importance of the fatigue outcome to patients was unclear. OBJECTIVE: To assess the importance of the OPTIMUM FSIQ-RMS-S results using data from an MS discrete choice experiment (DCE). METHODS: The DCE included components to correlate levels of physical and cognitive fatigue with FSIQ-RMS-S scores. Changes in relapses/year and time to MS progression equivalent to the treatment difference in fatigue in OPTIMUM were determined for similar fatigue levels as mean baseline fatigue in OPTIMUM. RESULTS: DCE participants would accept 0.06 more relapses/year or a 0.15–0.17 year decrease in time to MS progression for a 3.57-point difference in physical fatigue on the FSIQ-RMS-S. To improve cognitive fatigue by 3.57-points on the FSIQ-RMS-S, DCE participants would accept 0.09–0.10 more relapses/year or a 0.24–0.28 year decrease in time to MS progression. CONCLUSION: MS patients would accept 0.06 more relapses/year to change their fatigue by a similar magnitude as the between-treatment difference observed in the OPTIMUM trial. SAGE Publications 2022-12-22 2023-03 /pmc/articles/PMC9972232/ /pubmed/36550636 http://dx.doi.org/10.1177/13524585221140270 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 pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Papers Fox, Robert J Tervonen, Tommi Phillips-Beyer, Andrea Sidorenko, Tatiana Boyanova, Neli Brooks, Anne Hennessy, Brian Jamieson, Carol Levitan, Bennett The relevance of fatigue to relapse rate in multiple sclerosis: Applying patient preference data to the OPTIMUM trial |
title | The relevance of fatigue to relapse rate in multiple sclerosis:
Applying patient preference data to the OPTIMUM trial |
title_full | The relevance of fatigue to relapse rate in multiple sclerosis:
Applying patient preference data to the OPTIMUM trial |
title_fullStr | The relevance of fatigue to relapse rate in multiple sclerosis:
Applying patient preference data to the OPTIMUM trial |
title_full_unstemmed | The relevance of fatigue to relapse rate in multiple sclerosis:
Applying patient preference data to the OPTIMUM trial |
title_short | The relevance of fatigue to relapse rate in multiple sclerosis:
Applying patient preference data to the OPTIMUM trial |
title_sort | relevance of fatigue to relapse rate in multiple sclerosis:
applying patient preference data to the optimum trial |
topic | Original Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972232/ https://www.ncbi.nlm.nih.gov/pubmed/36550636 http://dx.doi.org/10.1177/13524585221140270 |
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