Published October 13, 2021 | Version v1
Publication

Anti-CD20 and natalizumab in highly active relapsing-remitting multiple sclerosis: the SWIFNA-20 comparative effectiveness study

Others:
Centre de Recherche en Transplantation et Immunologie (U1064 Inserm - CRTI) ; Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE) ; Université de Nantes (UN)-Université de Nantes (UN)
Centre de recherche en neurosciences de Lyon - Lyon Neuroscience Research Center (CRNL) ; Université Claude Bernard Lyon 1 (UCBL) ; Université de Lyon-Université de Lyon-Université Jean Monnet - Saint-Étienne (UJM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Observatoire Français de la Sclérose En Plaques [Lyon] (OFSEP)
Centre Hospitalier Universitaire de Nantes = Nantes University Hospital (CHU Nantes)
Hôpital de la Timone [CHU - APHM] (TIMONE)
Service de Neurologie [Strasbourg] ; Centre Hospitalier Universitaire [Strasbourg] (CHU Strasbourg) ; Les Hôpitaux Universitaires de Strasbourg (HUS)-Les Hôpitaux Universitaires de Strasbourg (HUS)-Nouvel Hôpital Civil de Strasbourg ; Les Hôpitaux Universitaires de Strasbourg (HUS)
CIC Strasbourg (Centre d'Investigation Clinique Plurithématique (CIC - P)) ; Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Nouvel Hôpital Civil de Strasbourg ; Les Hôpitaux Universitaires de Strasbourg (HUS)-Les Hôpitaux Universitaires de Strasbourg (HUS)-Hôpital de Hautepierre [Strasbourg]
CHU Montpellier ; Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)
Université de Montpellier (UM)
Neurocentre Magendie : Physiopathologie de la Plasticité Neuronale (U1215 Inserm - UB) ; Université de Bordeaux (UB)-Institut François Magendie-Institut National de la Santé et de la Recherche Médicale (INSERM)
CIC Bordeaux ; Université Bordeaux Segalen - Bordeaux 2-Institut National de la Santé et de la Recherche Médicale (INSERM)
Institut de Génomique Fonctionnelle (IGF) ; Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)
Service de Neurologie [CHU Nimes] (Pôle NIRR) ; Hôpital Universitaire Carémeau [Nîmes] (CHU Nîmes) ; Centre Hospitalier Universitaire de Nîmes (CHU Nîmes)-Centre Hospitalier Universitaire de Nîmes (CHU Nîmes)
Département Neurologie [CHU Toulouse] ; Pôle Neurosciences [CHU Toulouse] ; Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)
Centre Ressources et Compétences sclérose en plaques (CRC-SEP) [CHU Toulouse] (CRC-SEP Toulouse) ; Département Neurologie [CHU Toulouse] ; Pôle Neurosciences [CHU Toulouse] ; Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Pôle Neurosciences [CHU Toulouse] ; Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)
Service Neurologie [CHU Clermont-Ferrand] ; CHU Gabriel Montpied [Clermont-Ferrand] ; CHU Clermont-Ferrand-CHU Clermont-Ferrand-Pôle Médecine interne, Neurologie, Neurochirurgie, Ophtalmologie [CHU Clermont-Ferrand] (MNDO) ; CHU Gabriel Montpied [Clermont-Ferrand] ; CHU Clermont-Ferrand-CHU Clermont-Ferrand
Neuro-Dol (Neuro-Dol) ; Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Clermont Auvergne (UCA)
Institut du Cerveau = Paris Brain Institute (ICM) ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP] ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
CHU Saint-Antoine [AP-HP] ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
CHU Pitié-Salpêtrière [AP-HP] ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
CHU Rouen ; Normandie Université (NU)
Service de Neurologie [CHU Nice] ; Hôpital Pasteur [Nice] (CHU)-Centre Hospitalier Universitaire de Nice (CHU Nice)
Unité de Recherche Clinique de la Côte d'Azur (URRIS UR2CA) ; Centre Hospitalier Universitaire de Nice (CHU Nice)-Université Côte d'Azur (UniCA)
Service de Neurologie [CHU Caen] ; Université de Caen Normandie (UNICAEN) ; Normandie Université (NU)-Normandie Université (NU)-CHU Caen ; Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN)
Centre Hospitalier Universitaire de Saint-Etienne [CHU Saint-Etienne] (CHU ST-E)
CHU Trousseau [Tours] ; Centre Hospitalier Régional Universitaire de Tours (CHRU Tours)
Centre Hospitalier de Saint-Denis [Ile-de-France]
Hôpital universitaire Robert Debré [Reims] (CHU Reims)
Hôpital Dupuytren [CHU Limoges]
Université Claude Bernard Lyon 1 (UCBL) ; Université de Lyon
Hospices Civils de Lyon (HCL)
European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS)

Description

Background: Despite a second-line treatment with fingolimod (FNG), some patients with relapsing-remitting Multiple Sclerosis (RR-MS) may have residual disease activity. The current therapeutic strategy is based on the switch to either natalizumab (NTZ) or anti-CD20 (rituximab or ocrelizumab). To date the relative effectiveness of these two strategies has not been evaluated.Objective: Using an innovative statistical approach, our main objective was to describe the dynamics of the event rates (ER) on clinical outcomes and to study how NTZ or anti-CD20 affects these dynamics.Methods: From the 68 847 MS patients of the OFSEP database, 740 RRMS patients were treated with FNG and switched either to anti-CD20 (n=337) or NTZ (n=403) from the 1st January 2014. The primary outcome was the time to the first relapse within 24 months. The secondary outcomes were the time to EDSS worsening, proportion of patients with at least a new T2 lesion and the time to discontinuation. Dynamics of ER according to time were evaluated using multidimensional penalized hazard models, offering the opportunity to model the effects of covariates in a flexible way, accounting for non-linearity and interactions.Results: At baseline, patients were 37.7 +/- 9.9 years-old and 74.7% were women, with a median follow-up of 22.9 months after treatment switch. There was no difference between the two treatments on the occurrence of the first relapse. The monthly probability of a first relapse was 5.0% at baseline and 1.0% after 6 months. Regarding EDSS, in both groups, ER increased up to 6 months and then gradually decreased. There was no significant difference between the two treatments when adjusting for covariates. In addition, no difference in the proportion of patients with new T2 lesions at 24 months was observed. After 18 months of follow-up, there was a greater risk of NTZ discontinuation compared to anti-CD20 (adjusted HR=1.59; CI 95%: 1.02-2.49 at 19 months and HR=2.23; CI 95%: 1.15-4.35 at 24 months).Conclusion: This study did not show any difference between NTZ and anti-CD20 after FNG switch on disease activity, both clinically and radiologically, but did show that there was an optimal effect of both treatments after 6 months and more frequent NTZ discontinuation, probably due to seroconversions to JCV.

Abstract

International audience

Additional details

Created:
November 8, 2024
Modified:
November 8, 2024