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Multiple Sclerosis Relapses Following Cessation of Fingolimod
CB. Malpas, I. Roos, S. Sharmin, K. Buzzard, O. Skibina, H. Butzkueven, L. Kappos, F. Patti, R. Alroughani, D. Horakova, EK. Havrdova, G. Izquierdo, S. Eichau, S. Hodgkinson, P. Grammond, J. Lechner-Scott, T. Kalincik, MSBase Study Group
Language English Country New Zealand
Document type Journal Article
Grant support
1129189
National Health and Medical Research Council
1140766
National Health and Medical Research Council
1080518
National Health and Medical Research Council
NLK
ProQuest Central
from 2008-06-01 to 1 year ago
Health & Medicine (ProQuest)
from 2008-06-01 to 1 year ago
- MeSH
- Fingolimod Hydrochloride adverse effects MeSH
- Immunosuppressive Agents adverse effects MeSH
- Humans MeSH
- Recurrence MeSH
- Multiple Sclerosis, Relapsing-Remitting * drug therapy MeSH
- Multiple Sclerosis * MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
BACKGROUND: There is growing interest in the issue of disease reactivation in multiple sclerosis following fingolimod cessation. Relatively little is known about modifiers of the risk of post-cessation relapse, including the delay to commencement of new therapy and prior disease activity. OBJECTIVE: We aimed to determine the rate of relapse following cessation of fingolimod and to identify predictors of relapse following cessation. METHODS: Data were extracted from the MSBase registry in March 2019. Inclusion criteria were (a) clinically definite relapsing multiple sclerosis, (b) treatment with fingolimod for ≥ 12 months, (c) follow-up after cessation for ≥ 12 months, and (d) at least one Expanded Disability Status Scale score recorded in the 12 months before cessation. RESULTS: A total of 685 patients were identified who met criteria. The mean annualised relapse rate was 1.71 (95% CI 1.59, 1.85) in the year prior to fingolimod, 0.50 (95% CI 0.44, 0.55) on fingolimod and 0.43 (95% CI 0.38, 0.49) after fingolimod. Of these, 218 (32%) patients experienced a relapse in the first 12 months. Predictors of a higher relapse rate in the first year were: younger age at fingolimod cessation, higher relapse rate in the year prior to cessation, delaying commencement of new therapy and switching to low-efficacy therapy. CONCLUSIONS: Disease reactivation following fingolimod cessation is more common in younger patients, those with greater disease activity prior to cessation and in those who switch to a low-efficacy therapy.
Box Hill Hospital Melbourne VIC Australia
Central Clinical School Monash University Melbourne VIC Australia
CISSS ChaudiËre Appalache Levis QC Canada
Department of Medicine CORe University of Melbourne Melbourne VIC Australia
Department of Neurology Box Hill Hospital Monash University Melbourne VIC Australia
Department of Neurology John Hunter Hospital Hunter New England Health Newcastle NSW Australia
Department of Neurology Royal Melbourne Hospital Melbourne MS Centre Melbourne VIC Australia
Department of Neurology The Alfred Hospital Melbourne VIC Australia
Division of Neurology Department of Medicine Amiri Hospital Sharq Kuwait
GF Ingrassia Department University of Catania Catania Italy
Hospital Universitario Virgen Macarena Sevilla Spain
Liverpool Hospital Sydney NSW Australia
Monash University Melbourne VIC Australia
Policlinico G Rodolico Catania Italy
Royal Melbourne Hospital Melbourne MS Centre Melbourne VIC Australia
School of Medicine and Public Health University of Newcastle Newcastle NSW Australia
References provided by Crossref.org
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- $a BACKGROUND: There is growing interest in the issue of disease reactivation in multiple sclerosis following fingolimod cessation. Relatively little is known about modifiers of the risk of post-cessation relapse, including the delay to commencement of new therapy and prior disease activity. OBJECTIVE: We aimed to determine the rate of relapse following cessation of fingolimod and to identify predictors of relapse following cessation. METHODS: Data were extracted from the MSBase registry in March 2019. Inclusion criteria were (a) clinically definite relapsing multiple sclerosis, (b) treatment with fingolimod for ≥ 12 months, (c) follow-up after cessation for ≥ 12 months, and (d) at least one Expanded Disability Status Scale score recorded in the 12 months before cessation. RESULTS: A total of 685 patients were identified who met criteria. The mean annualised relapse rate was 1.71 (95% CI 1.59, 1.85) in the year prior to fingolimod, 0.50 (95% CI 0.44, 0.55) on fingolimod and 0.43 (95% CI 0.38, 0.49) after fingolimod. Of these, 218 (32%) patients experienced a relapse in the first 12 months. Predictors of a higher relapse rate in the first year were: younger age at fingolimod cessation, higher relapse rate in the year prior to cessation, delaying commencement of new therapy and switching to low-efficacy therapy. CONCLUSIONS: Disease reactivation following fingolimod cessation is more common in younger patients, those with greater disease activity prior to cessation and in those who switch to a low-efficacy therapy.
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