BEST-MS: A prospective head-to-head comparative study of natalizumab and fingolimod in active relapsing MS.


Journal

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

Informations de publication

Date de publication:
09 2021
Historique:
pubmed: 31 10 2020
medline: 25 2 2023
entrez: 30 10 2020
Statut: ppublish

Résumé

There are few head-to-head studies to compare highly active treatments in multiple sclerosis (MS). The aim of this study was to compare the effectiveness between natalizumab (NTZ) and fingolimod (FTY) in active relapsing-remitting MS. Best Escalation STrategy in Multiple Sclerosis (BEST-MS) is a multicentric, prospective study with a 12-month follow-up including patients with active MS. Treatment choice was at the discretion of physician. Clinical and magnetic resonance imaging (MRI) data were collected at baseline and at 12 months. The primary outcome was the proportion of patients reaching no evidence of disease activity (NEDA) at 12 months. Secondary outcomes included annualized relapse rate and MRI activity. A total of 223 patients were included (NTZ: 109 and FTY: 114). Treatment groups were well balanced at baseline. Proportion of NEDA patients was 47.8% in NTZ group versus 30.4% in FTY group ( BEST-MS is a prospective study that compared head-to-head the effectiveness of NTZ and FTY in active relapsing-remitting MS. Our results suggest a superiority of NTZ over FTY.

Sections du résumé

BACKGROUND
There are few head-to-head studies to compare highly active treatments in multiple sclerosis (MS).
OBJECTIVE
The aim of this study was to compare the effectiveness between natalizumab (NTZ) and fingolimod (FTY) in active relapsing-remitting MS.
METHOD
Best Escalation STrategy in Multiple Sclerosis (BEST-MS) is a multicentric, prospective study with a 12-month follow-up including patients with active MS. Treatment choice was at the discretion of physician. Clinical and magnetic resonance imaging (MRI) data were collected at baseline and at 12 months. The primary outcome was the proportion of patients reaching no evidence of disease activity (NEDA) at 12 months. Secondary outcomes included annualized relapse rate and MRI activity.
RESULTS
A total of 223 patients were included (NTZ: 109 and FTY: 114). Treatment groups were well balanced at baseline. Proportion of NEDA patients was 47.8% in NTZ group versus 30.4% in FTY group (
CONCLUSION
BEST-MS is a prospective study that compared head-to-head the effectiveness of NTZ and FTY in active relapsing-remitting MS. Our results suggest a superiority of NTZ over FTY.

Identifiants

pubmed: 33124504
doi: 10.1177/1352458520969145
doi:

Substances chimiques

Natalizumab 0
Fingolimod Hydrochloride G926EC510T

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1556-1563

Auteurs

Mikael Cohen (M)

Service de Neurologie, CRCSEP, Unité de Recherche Clinique Cote d'Azur (UR2CA), Centre Hospitalier Universitaire Pasteur 2, Nice, France.

Lydiane Mondot (L)

Service de Radiologie, Unité de Recherche Clinique Cote d'Azur (UR2CA), Centre Hospitalier Universitaire Pasteur 2, Nice, France.

Florence Bucciarelli (F)

Neurosciences Department, CRCSEP, University Hospital of Toulouse, Toulouse, France/INSERM U1043-CNRS UMR 5282, Centre de Physiopathologie Toulouse, Toulouse, France.

Béatrice Pignolet (B)

Neurosciences Department, CRCSEP, University Hospital of Toulouse, Toulouse, France/INSERM U1043-CNRS UMR 5282, Centre de Physiopathologie Toulouse, Toulouse, France.

David-Axel Laplaud (DA)

CRTI-INSERM U1064, CIC 1413, Service de Neurologie, CHU Nantes, Nantes, France.

Sandrine Wiertlewski (S)

CRTI-INSERM U1064, CIC 1413, Service de Neurologie, CHU Nantes, Nantes, France.

Bruno Brochet (B)

Service de Neurologie, CRC SEP, Centre Hospitalier Universitaire (CHU) de Bordeaux, Bordeaux, France.

Aurélie Ruet (A)

Service de Neurologie, CRC SEP, Centre Hospitalier Universitaire (CHU) de Bordeaux, Bordeaux, France.

Gilles Defer (G)

Service de Neurologie, CHU de Caen, Avenue de la Côte de Nacre, Caen, France.

Nathalie Derache (N)

Service de Neurologie, CHU de Caen, Avenue de la Côte de Nacre, Caen, France.

Patrick Vermersch (P)

Univ. Lille, INSERM U1172, CHU Lille, FHU Imminent, Lille, France.

Hélène Zephir (H)

Univ. Lille, INSERM U1172, CHU Lille, FHU Imminent, Lille, France.

Marc Debouverie (M)

CHRU-Nancy, INSERM, Université de Lorraine, CIC, Epidémiologie Clinique, Nancy, France.

Guillaume Mathey (G)

CHRU-Nancy, INSERM, Université de Lorraine, CIC, Epidémiologie Clinique, Nancy, France.

Eric Berger (E)

Service de Neurologie, CHU de Besançon, Besançon, France.

Chrystelle Cappé (C)

Centre d'investigation clinique, CHU de Besançon, Besançon, France.

Pierre Labauge (P)

CHU de Montpellier, MS Unit, Montpellier, France.

Clarisse Carra (C)

CHU de Montpellier, MS Unit, Montpellier, France.

Jérôme De Seze (J)

Clinical Investigation Center, Department of Neurology, CHU de Strasbourg, INSERM 1434, Strasbourg, France.

Kevin Bigaut (K)

Clinical Investigation Center, Department of Neurology, CHU de Strasbourg, INSERM 1434, Strasbourg, France.

David Brassat (D)

Neurosciences Department, CRCSEP, University Hospital of Toulouse, Toulouse, France/INSERM U1043-CNRS UMR 5282, Centre de Physiopathologie Toulouse, Toulouse, France.

Christine Lebrun-Frenay (C)

Service de Neurologie, CRCSEP, Unité de Recherche Clinique Cote d'Azur (UR2CA), Centre Hospitalier Universitaire Pasteur 2, Nice, France.

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Classifications MeSH