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Dimethyl fumarate vs fingolimod following different pretreatments: A retrospective study
OBJECTIVE: Despite frequent use of fingolimod (FTY) and dimethyl fumarate (DMF), studies comparing clinical efficacy and withdrawal rates of DMF and FTY concerning different pretreatment situations are rare. The aim of our study was to compare relapse occurrence and withdrawal rates of DMF and FTY i...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6984136/ https://www.ncbi.nlm.nih.gov/pubmed/31937596 http://dx.doi.org/10.1212/NXI.0000000000000660 |
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author | Diem, Lara Daponte, Ariadne Findling, Oliver Miclea, Andrei Briner, Myriam Salmen, Anke Gold, Ralf Kilidireas, Constantinos Chan, Andrew Evangelopoulos, Maria Elftheria Hoepner, Robert |
author_facet | Diem, Lara Daponte, Ariadne Findling, Oliver Miclea, Andrei Briner, Myriam Salmen, Anke Gold, Ralf Kilidireas, Constantinos Chan, Andrew Evangelopoulos, Maria Elftheria Hoepner, Robert |
author_sort | Diem, Lara |
collection | PubMed |
description | OBJECTIVE: Despite frequent use of fingolimod (FTY) and dimethyl fumarate (DMF), studies comparing clinical efficacy and withdrawal rates of DMF and FTY concerning different pretreatment situations are rare. The aim of our study was to compare relapse occurrence and withdrawal rates of DMF and FTY in different pretreatment situations. METHODS: Patients from 4 European centers were retrospectively identified and followed until the 1st relapse after treatment start or if no relapse occurred for a maximum of 2 years. Cox regression analyses adjusted for relapsing-remitting MS (RRMS) disease duration, sex, and region were performed for the following pretreatment situations: treatment naive or injectables or DMF/FTY or natalizumab. RESULTS: Seven hundred thirty-two patients with RRMS (female/male: 2.4:1.0; DMF n = 409, FTY n = 323) were analyzed. Compared with FTY-treated patients, DMF-treated patients discontinued treatment more frequently mainly because of side effects (DMF/FTY: 29.3%/20.7%). Clinical relapses occurred in 24.5% of the patients within 24 months. Survival analysis demonstrated that compared with FTY treatment, DMF treatment was associated with an adjusted hazard ratio (aHR) for occurrence of relapse of 1.9 (95% CI 1.4–2.6, p < 0.001, n = 732). Stratification into pretreatment groups unmasked a higher relapse risk in DMF patients pretreated with natalizumab (aHR [95% CI] 4.5 [1.9–10.8], p = 0.001, n = 122) or to a lesser extend also in treatment-naive patients (aHR [95% CI] 1.9 [1.01–3.6], p = 0.045, n = 230). No differences were observed in patients pretreated with injectables or the respective other oral drug (injectables: p > 0.05, n = 341; other oral: p > 0.05, n = 39). CONCLUSIONS: DMF treatment was associated with higher clinical disease activity compared with FTY treatment. A subgroup analysis suggested beneficial effects of FTY in treatment-naive and patients pretreated with natalizumab. |
format | Online Article Text |
id | pubmed-6984136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-69841362020-02-10 Dimethyl fumarate vs fingolimod following different pretreatments: A retrospective study Diem, Lara Daponte, Ariadne Findling, Oliver Miclea, Andrei Briner, Myriam Salmen, Anke Gold, Ralf Kilidireas, Constantinos Chan, Andrew Evangelopoulos, Maria Elftheria Hoepner, Robert Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: Despite frequent use of fingolimod (FTY) and dimethyl fumarate (DMF), studies comparing clinical efficacy and withdrawal rates of DMF and FTY concerning different pretreatment situations are rare. The aim of our study was to compare relapse occurrence and withdrawal rates of DMF and FTY in different pretreatment situations. METHODS: Patients from 4 European centers were retrospectively identified and followed until the 1st relapse after treatment start or if no relapse occurred for a maximum of 2 years. Cox regression analyses adjusted for relapsing-remitting MS (RRMS) disease duration, sex, and region were performed for the following pretreatment situations: treatment naive or injectables or DMF/FTY or natalizumab. RESULTS: Seven hundred thirty-two patients with RRMS (female/male: 2.4:1.0; DMF n = 409, FTY n = 323) were analyzed. Compared with FTY-treated patients, DMF-treated patients discontinued treatment more frequently mainly because of side effects (DMF/FTY: 29.3%/20.7%). Clinical relapses occurred in 24.5% of the patients within 24 months. Survival analysis demonstrated that compared with FTY treatment, DMF treatment was associated with an adjusted hazard ratio (aHR) for occurrence of relapse of 1.9 (95% CI 1.4–2.6, p < 0.001, n = 732). Stratification into pretreatment groups unmasked a higher relapse risk in DMF patients pretreated with natalizumab (aHR [95% CI] 4.5 [1.9–10.8], p = 0.001, n = 122) or to a lesser extend also in treatment-naive patients (aHR [95% CI] 1.9 [1.01–3.6], p = 0.045, n = 230). No differences were observed in patients pretreated with injectables or the respective other oral drug (injectables: p > 0.05, n = 341; other oral: p > 0.05, n = 39). CONCLUSIONS: DMF treatment was associated with higher clinical disease activity compared with FTY treatment. A subgroup analysis suggested beneficial effects of FTY in treatment-naive and patients pretreated with natalizumab. Lippincott Williams & Wilkins 2020-01-14 /pmc/articles/PMC6984136/ /pubmed/31937596 http://dx.doi.org/10.1212/NXI.0000000000000660 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Article Diem, Lara Daponte, Ariadne Findling, Oliver Miclea, Andrei Briner, Myriam Salmen, Anke Gold, Ralf Kilidireas, Constantinos Chan, Andrew Evangelopoulos, Maria Elftheria Hoepner, Robert Dimethyl fumarate vs fingolimod following different pretreatments: A retrospective study |
title | Dimethyl fumarate vs fingolimod following different pretreatments: A retrospective study |
title_full | Dimethyl fumarate vs fingolimod following different pretreatments: A retrospective study |
title_fullStr | Dimethyl fumarate vs fingolimod following different pretreatments: A retrospective study |
title_full_unstemmed | Dimethyl fumarate vs fingolimod following different pretreatments: A retrospective study |
title_short | Dimethyl fumarate vs fingolimod following different pretreatments: A retrospective study |
title_sort | dimethyl fumarate vs fingolimod following different pretreatments: a retrospective study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6984136/ https://www.ncbi.nlm.nih.gov/pubmed/31937596 http://dx.doi.org/10.1212/NXI.0000000000000660 |
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