Therapy of highly active pediatric multiple sclerosis.


Journal

Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185

Informations de publication

Date de publication:
01 2019
Historique:
pubmed: 22 9 2017
medline: 16 1 2020
entrez: 22 9 2017
Statut: ppublish

Résumé

Study aims were to determine the frequency of highly active disease in pediatric multiple sclerosis (MS), the response to natalizumab (NTZ) and fingolimod (FTY) treatment, and the impact of current treatment modalities on the clinical course. Retrospective single-center study in the German Center for MS in Childhood and Adolescence. Of 144 patients with first MS manifestation between 2011 and 2015, 41.6% fulfilled the criteria for highly active MS. In total, 55 patients treated with NTZ and 23 with FTY demonstrated a significant reduction in relapse rate (NTZ: 95.2%, FTY: 75%), new T2 lesions (NTZ: 97%, FTY: 81%), and contrast-enhancing lesions (NTZ: 97%, FTY: 93%). However, seven patients switched from NTZ to FTY experienced an increase in disease activity. Comparing pediatric MS patients treated in 2005 with those treated in 2015 showed a 46% reduction in relapse rate and a 44% reduction in mean Expanded Disability Status Scale (EDSS). The rate of highly active disease among pediatric MS patients is high; more than 40% in our cohort. Response to NTZ and FTY treatment is similar if not better than observed in adults. Current treatment modalities including earlier treatment initiation and the introduction of NTZ and FTY have significantly improved the clinical course of pediatric MS.

Identifiants

pubmed: 28933245
doi: 10.1177/1352458517732843
doi:

Substances chimiques

Immunologic Factors 0
Natalizumab 0
Fingolimod Hydrochloride G926EC510T

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

72-80

Auteurs

Peter Huppke (P)

Department of Pediatrics and Pediatric Neurology, University Medical Center Göttingen, Georg-August-Universität Göttingen, Göttingen, Germany.

Brenda Huppke (B)

Department of Pediatrics and Pediatric Neurology, University Medical Center Göttingen, Georg-August-Universität Göttingen, Göttingen, Germany.

David Ellenberger (D)

Department of Medical Statistics, University Medical Center Göttingen, Georg-August-Universität Göttingen, Göttingen, Germany.

Kevin Rostasy (K)

Children's Hospital Datteln, Witten/Herdecke University, Witten, Germany.

Hannah Hummel (H)

Department of Pediatrics and Pediatric Neurology, University Medical Center Göttingen, Georg-August-Universität Göttingen, Göttingen, Germany.

Wiebke Stark (W)

Department of Pediatrics and Pediatric Neurology, University Medical Center Göttingen, Georg-August-Universität Göttingen, Göttingen, Germany.

Wolfgang Brück (W)

Institute of Neuropathology, University Medical Center Göttingen, Georg-August-Universität Göttingen, Göttingen, Germany.

Jutta Gärtner (J)

Department of Pediatrics and Pediatric Neurology, University Medical Center Göttingen, Georg-August-Universität Göttingen, Göttingen, Germany.

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Classifications MeSH