Risk of T

cohort study disease-modifying therapy multiple sclerosis safety treatment discontinuation

Journal

Brain communications
ISSN: 2632-1297
Titre abrégé: Brain Commun
Pays: England
ID NLM: 101755125

Informations de publication

Date de publication:
2024
Historique:
received: 28 03 2023
revised: 25 10 2023
accepted: 01 01 2024
medline: 12 1 2024
pubmed: 12 1 2024
entrez: 12 1 2024
Statut: epublish

Résumé

Fingolimod is a frequently used disease-modifying therapy in relapsing-remitting multiple sclerosis. However, case reports and small observational studies indicate a highly increased risk of disease reactivation after discontinuation. We aimed to investigate the risk of radiological disease reactivation in patients discontinuing fingolimod. We performed a nationwide cohort study in Denmark, including patients who discontinued fingolimod between January 2014 and January 2023. Eligibility was a diagnosis with relapsing-remitting multiple sclerosis and two MRIs performed respectively within 1 year before and after discontinuing fingolimod. The included patients were compared with those discontinuing dimethyl fumarate with the same eligibility criteria in an unadjusted and matched propensity score analysis. Matching was done on age, sex, Expanded Disability Status Scale, MRI data, cause for treatment discontinuation, treatment duration and relapse rate. The main outcome was the presence of new T

Identifiants

pubmed: 38214014
doi: 10.1093/braincomms/fcad358
pii: fcad358
pmc: PMC10783644
doi:

Types de publication

Journal Article

Langues

eng

Pagination

fcad358

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the Guarantors of Brain.

Déclaration de conflit d'intérêts

M.F.W.-H. has served on the scientific advisory board for Sanofi and has received honoraria for lecturing for Novartis and Sanofi. R.P.H. has served on the scientific advisory board for Novartis and received honoraria for lecturing for Novartis and Sanofi. A.H. has served on the scientific advisory board for Merck and received honoraria for lecturing for Biogen and Merck. A.R.L. reports no competing interests. M.M. has served on the scientific advisory board for Biogen, Sanofi, Roche, Novartis, Merck and AbbVie, has received honoraria for lecturing from Biogen, Merck, Novartis, Sanofi and Genzyme and has received research support and support for congress participation from Biogen, Genzyme, Teva, Roche, Merck and Novartis.

Auteurs

Malthe Faurschou Wandall-Holm (MF)

Department of Neurology, Danish Multiple Sclerosis Registry, Copenhagen University Hospital-Rigshospitalet, Glostrup DK-2600, Denmark.

Rolf Pringler Holm (RP)

Department of Neurology, Danish Multiple Sclerosis Registry, Copenhagen University Hospital-Rigshospitalet, Glostrup DK-2600, Denmark.

Alex Heick (A)

Department of Neurology, Danish Multiple Sclerosis Center, Copenhagen University Hospital-Rigshospitalet, Glostrup DK-2600, Denmark.

Annika Reynberg Langkilde (AR)

Department of Radiology, Diagnostic Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen DK-2100, Denmark.

Melinda Magyari (M)

Department of Neurology, Danish Multiple Sclerosis Registry, Copenhagen University Hospital-Rigshospitalet, Glostrup DK-2600, Denmark.
Department of Neurology, Danish Multiple Sclerosis Center, Copenhagen University Hospital-Rigshospitalet, Glostrup DK-2600, Denmark.

Classifications MeSH