Switching from natalizumab to fingolimod treatment in multiple sclerosis: real life data from the Austrian MS Treatment Registry.
Fingolimod
Multiple sclerosis
Natalizumab
Switch
Journal
Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161
Informations de publication
Date de publication:
Nov 2019
Nov 2019
Historique:
received:
24
05
2019
accepted:
09
07
2019
revised:
08
07
2019
pubmed:
18
7
2019
medline:
21
3
2020
entrez:
18
7
2019
Statut:
ppublish
Résumé
To compare the efficacy of natalizumab (NTZ) and fingolimod (FTY) in the treatment of relapsing-remitting multiple sclerosis (MS) in sequential use in common and as a function of transition periods in a nationwide observational cohort using prospectively collected data from a real-life setting. We included 195 patients from the Austrian MS Treatment Registry, who had started treatment with NTZ at any time since 2006 and stayed on NTZ for at least 24 months, switched afterwards within 1 year to FTY and stayed on FTY for at least another 12 months. Transition periods between NTZ and FTY were grouped into three different intervals: < 3 months (135 patients), 3-6 months (44 patients), and 6-12 months (16 patients). Estimated mean annualized relapse rates (ARR) over a mean treatment period of 44 months were 0.26 for NTZ and 0.32 for FTY (p = 0.381) over 46 months. In the treatment gap, differences were found concerning the relapse probability, seven (5.2%) patients in the < 3 months group, six (13.6%) in thef 3-6 months group, and seven (43.8%) in the 6-12 months group (p < 0.001). After this treatment gap, no significant differences concerning ARR, EDSS change, EDSS progression, and regression were observed regardless the proceeding transition periods. Significantly higher efficacy of NTZ compared to FTY in sequential use was found regarding EDSS change, EDSS progression, and EDSS regression sustained for 12 and 24 weeks. First, we here show an increased short-time risk for relapses during the treatment gap between NTZ and FTY therapy, dependent on the length of transition time. Second, the disease course after switching to FTY remained stable in the long-term evaluation. Therefore, switching from NTZ to FTY in a real-world setting appears efficacious and safe, but this data advocate for a short switching gap of 3 months or less.
Identifiants
pubmed: 31312958
doi: 10.1007/s00415-019-09464-0
pii: 10.1007/s00415-019-09464-0
doi:
Substances chimiques
Immunologic Factors
0
Natalizumab
0
Fingolimod Hydrochloride
G926EC510T
Types de publication
Journal Article
Observational Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
2672-2677Commentaires et corrections
Type : ErratumIn
Références
Mult Scler. 2015 May;21(6):786-90
pubmed: 25257618
Pract Neurol. 2016 Oct;16(5):389-93
pubmed: 27114560
JAMA Neurol. 2014 Apr;71(4):436-41
pubmed: 24566807
Acta Neurol Scand. 2013 Aug;128(2):e6-e10
pubmed: 23336398
Acta Neurol Scand. 2018 Feb;137(2):181-187
pubmed: 29159801
Ther Adv Neurol Disord. 2018 Aug 09;11:1756286418791103
pubmed: 30116299
N Engl J Med. 2010 Feb 4;362(5):402-15
pubmed: 20089954
Neurology. 2011 May 31;76(22):1858-65
pubmed: 21543733
Lancet Neurol. 2014 Jun;13(6):545-56
pubmed: 24685276
Eur Neurol. 2017;77(3-4):130-136
pubmed: 28052269
N Engl J Med. 2006 Mar 2;354(9):899-910
pubmed: 16510744
J Neurol Sci. 2011 Sep 15;308(1-2):98-102
pubmed: 21665227
J Neurol Sci. 2018 Jul 15;390:89-93
pubmed: 29801915
J Neurol. 2013 May;260(5):1382-7
pubmed: 23266894
Ann Neurol. 2014 Dec;76(6):802-12
pubmed: 25273271
Acta Neurol Scand. 2014 Aug;130(2):97-102
pubmed: 24720783
Neurology. 2014 Apr 8;82(14):1204-11
pubmed: 24610329
N Engl J Med. 2010 Feb 4;362(5):387-401
pubmed: 20089952
Mult Scler. 2018 Oct;24(11):1453-1460
pubmed: 28823223