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The ACROSS study: Long-term efficacy of fingolimod in patients with relapsing–remitting multiple sclerosis

BACKGROUND: In chronic diseases such as multiple sclerosis requiring lifelong treatment, studies on long-term outcomes are important. OBJECTIVE: To assess disability and magnetic resonance imaging-related outcomes in relapsing multiple sclerosis patients from a Phase 2 study of fingolimod 10 or more...

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Autores principales: Derfuss, T, Sastre-Garriga, J, Montalban, X, Rodegher, M, Wuerfel, J, Gaetano, L, Tomic, D, Azmon, A, Wolf, C, Kappos, L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132565/
https://www.ncbi.nlm.nih.gov/pubmed/32284874
http://dx.doi.org/10.1177/2055217320907951
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author Derfuss, T
Sastre-Garriga, J
Montalban, X
Rodegher, M
Wuerfel, J
Gaetano, L
Tomic, D
Azmon, A
Wolf, C
Kappos, L
author_facet Derfuss, T
Sastre-Garriga, J
Montalban, X
Rodegher, M
Wuerfel, J
Gaetano, L
Tomic, D
Azmon, A
Wolf, C
Kappos, L
author_sort Derfuss, T
collection PubMed
description BACKGROUND: In chronic diseases such as multiple sclerosis requiring lifelong treatment, studies on long-term outcomes are important. OBJECTIVE: To assess disability and magnetic resonance imaging-related outcomes in relapsing multiple sclerosis patients from a Phase 2 study of fingolimod 10 or more years after randomization and to compare outcomes in patients who had a higher fingolimod exposure versus those with a lower fingolimod exposure. METHODS: ACROSS was a cross-sectional follow-up study of patients originally enrolled in a Phase 2 fingolimod proof-of-concept study (NCT00333138). Disability and magnetic resonance imaging-related outcomes were assessed in patients grouped according to fingolimod treatment duration, based on an arbitrary cut-off: ≥8 years (high exposure) and <8 years (low exposure). RESULTS: Overall, 175/281 (62%) patients participated in ACROSS; 104 (59%) of these were classified “high exposure.” At 10 years, patients in the high-exposure group had smaller increases in Expanded Disability Status Scale (+0.55 vs. +1.21), and lower frequencies of disability progression (34.7% vs. 56.1%), wheelchair use (4.8% vs. 16.9%), or transition to secondary progressive multiple sclerosis (9.6% vs. 22.5%) than those in the low-exposure group. The high-exposure patients also had less progression in most magnetic resonance imaging-related outcomes. CONCLUSION: After 10 years of fingolimod treatment, disability progression was lower in the high-exposure group than in the low-exposure group.
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spelling pubmed-71325652020-04-13 The ACROSS study: Long-term efficacy of fingolimod in patients with relapsing–remitting multiple sclerosis Derfuss, T Sastre-Garriga, J Montalban, X Rodegher, M Wuerfel, J Gaetano, L Tomic, D Azmon, A Wolf, C Kappos, L Mult Scler J Exp Transl Clin Original Research Paper BACKGROUND: In chronic diseases such as multiple sclerosis requiring lifelong treatment, studies on long-term outcomes are important. OBJECTIVE: To assess disability and magnetic resonance imaging-related outcomes in relapsing multiple sclerosis patients from a Phase 2 study of fingolimod 10 or more years after randomization and to compare outcomes in patients who had a higher fingolimod exposure versus those with a lower fingolimod exposure. METHODS: ACROSS was a cross-sectional follow-up study of patients originally enrolled in a Phase 2 fingolimod proof-of-concept study (NCT00333138). Disability and magnetic resonance imaging-related outcomes were assessed in patients grouped according to fingolimod treatment duration, based on an arbitrary cut-off: ≥8 years (high exposure) and <8 years (low exposure). RESULTS: Overall, 175/281 (62%) patients participated in ACROSS; 104 (59%) of these were classified “high exposure.” At 10 years, patients in the high-exposure group had smaller increases in Expanded Disability Status Scale (+0.55 vs. +1.21), and lower frequencies of disability progression (34.7% vs. 56.1%), wheelchair use (4.8% vs. 16.9%), or transition to secondary progressive multiple sclerosis (9.6% vs. 22.5%) than those in the low-exposure group. The high-exposure patients also had less progression in most magnetic resonance imaging-related outcomes. CONCLUSION: After 10 years of fingolimod treatment, disability progression was lower in the high-exposure group than in the low-exposure group. SAGE Publications 2020-03-30 /pmc/articles/PMC7132565/ /pubmed/32284874 http://dx.doi.org/10.1177/2055217320907951 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: 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 Paper
Derfuss, T
Sastre-Garriga, J
Montalban, X
Rodegher, M
Wuerfel, J
Gaetano, L
Tomic, D
Azmon, A
Wolf, C
Kappos, L
The ACROSS study: Long-term efficacy of fingolimod in patients with relapsing–remitting multiple sclerosis
title The ACROSS study: Long-term efficacy of fingolimod in patients with relapsing–remitting multiple sclerosis
title_full The ACROSS study: Long-term efficacy of fingolimod in patients with relapsing–remitting multiple sclerosis
title_fullStr The ACROSS study: Long-term efficacy of fingolimod in patients with relapsing–remitting multiple sclerosis
title_full_unstemmed The ACROSS study: Long-term efficacy of fingolimod in patients with relapsing–remitting multiple sclerosis
title_short The ACROSS study: Long-term efficacy of fingolimod in patients with relapsing–remitting multiple sclerosis
title_sort across study: long-term efficacy of fingolimod in patients with relapsing–remitting multiple sclerosis
topic Original Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132565/
https://www.ncbi.nlm.nih.gov/pubmed/32284874
http://dx.doi.org/10.1177/2055217320907951
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