Comparative Effectiveness of Natalizumab Versus Anti-CD20 in Highly Active Relapsing-Remitting Multiple Sclerosis After Fingolimod Withdrawal.


Journal

Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
ISSN: 1878-7479
Titre abrégé: Neurotherapeutics
Pays: United States
ID NLM: 101290381

Informations de publication

Date de publication:
03 2022
Historique:
accepted: 07 02 2022
pubmed: 27 2 2022
medline: 28 6 2022
entrez: 26 2 2022
Statut: ppublish

Résumé

In France, two therapeutic strategies can be offered after fingolimod (FNG) withdrawal to highly active relapsing-remitting multiple sclerosis (RRMS) patients: natalizumab (NTZ) or anti-CD20. We compared the effectiveness of these two strategies as a switch for FNG within the OFSEP database. The primary endpoint was the time to first relapse. Other outcomes were the relapse rates over 3-month periods, time to worsening the EDSS score, proportion of patients with worsened 24-month MRI, time to treatment discontinuation, and incidence rates of serious adverse events. The dynamics of event rates over time were modeled using multidimensional penalized splines, allowing the possibility to model the effects of covariates in a flexible way, considering non-linearity and interactions. A total of 740 patients were included (337 under anti-CD20 and 403 under NTZ). There was no difference between the two treatments regarding the dynamic of the first occurrence of relapse, with a monthly probability of 5.0% at initiation and 1.0% after 6 months. The rate of EDSS worsening increased in both groups until 6 months and then decreased. No difference in the proportion of patients with new T2 lesions at 24 months was observed. After 18 months of follow-up, a greater risk of NTZ discontinuation was found compared to anti-CD20. This study showed no difference between NTZ and anti-CD20 after the FNG switch regarding the clinical and radiological activity. The effect of these treatments was optimal after 6 months and there was more frequent discontinuation of NTZ after 18 months, probably mainly related to JC virus seroconversions.

Identifiants

pubmed: 35217934
doi: 10.1007/s13311-022-01202-1
pii: 10.1007/s13311-022-01202-1
pmc: PMC9226262
doi:

Substances chimiques

Antigens, CD20 0
Immunologic Factors 0
Immunosuppressive Agents 0
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

476-490

Informations de copyright

© 2022. The American Society for Experimental NeuroTherapeutics, Inc.

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Auteurs

Fabien Rollot (F)

Université de Lyon, Université Claude Bernard, Lyon 1, Lyon, France. Fabien.rollot@chu-lyon.fr.
Service de Neurologie, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, sclérose en plaques, pathologies de la myéline et neuro-inflammation, Bron, France. Fabien.rollot@chu-lyon.fr.
Centre de Recherche en Neurosciences de Lyon, Observatoire Français de La Sclérose en Plaques, INSERM 1028 et CNRS UMR 5292, Lyon, France. Fabien.rollot@chu-lyon.fr.
EUGENE DEVIC EDMUS Foundation Against Multiple Sclerosis, State-Approved Foundation, Bron, France. Fabien.rollot@chu-lyon.fr.

Justine Couturier (J)

Service de Neurologie, CHU Nantes, Nantes, France.

Romain Casey (R)

Université de Lyon, Université Claude Bernard, Lyon 1, Lyon, France.
Service de Neurologie, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, sclérose en plaques, pathologies de la myéline et neuro-inflammation, Bron, France.
Centre de Recherche en Neurosciences de Lyon, Observatoire Français de La Sclérose en Plaques, INSERM 1028 et CNRS UMR 5292, Lyon, France.
EUGENE DEVIC EDMUS Foundation Against Multiple Sclerosis, State-Approved Foundation, Bron, France.

Sandrine Wiertlewski (S)

Service de Neurologie, CHU Nantes, Nantes, France.
INSERM, CIC 0004, CRTI-INSERM UMR U1064, Nantes, France.

Marc Debouverie (M)

Service de Neurologie, Centre Hospitalier Régional Et Universitaire de Nancy, Université de Lorraine, 4360 APEMAC, Vandoeuvre-Lès-Nancy, EA, France.

Jean Pelletier (J)

Aix Marseille University, APHM, Hôpital de La Timone, Pôle de Neurosciences Cliniques, Service de Neurologie, CEMEREM, 13005, Marseille, France.

Jérôme De Sèze (J)

Service de Neurologie Et Centre d'Investigation Clinique, CHU de Strasbourg, INSERM 1434, Strasbourg, France.

Pierre Labauge (P)

Service de Neurologie, CHU de Montpellier, Montpellier, France.

Aurélie Ruet (A)

Service de Neurologie, CHU de Bordeaux, Bordeaux, France.
Université de Bordeaux, INSERM, Neurocentre Magendie, U1215, Bordeaux, France.

Eric Thouvenot (E)

Service de Neurologie, CHU de Nîmes, Nîmes, France.
Institut de Génomique Fonctionnelle, Université de Montpellier, CNRS, INSERM, Montpellier, France.

Jonathan Ciron (J)

Service de Neurologie, CHU de Toulouse, Hôpital Pierre-Paul Riquet, CRC-SEP, Toulouse, France.
Institut Toulousain Des Maladies Infectieuses Et Inflammatoires (Infinity), INSERM UMR 1291, CNRS UMR 5051, Université Toulouse III, Toulouse, France.

Eric Berger (E)

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

Olivier Gout (O)

Service de Neurologie, Hôpital Fondation A de Rothschild, Paris, France.

Pierre Clavelou (P)

Service de Neurologie, CHU de Clermont-Ferrand, Clermont-Ferrand, France.

Bruno Stankoff (B)

Service de Neurologie, CHU Saint-Antoine, Paris, France.

Olivier Casez (O)

Service de Neurologie, CHU de Grenoble, Grenoble, France.

Bertrand Bourre (B)

Service de Neurologie, CHU de Rouen, Rouen, France.

Hélène Zephir (H)

Pôle Des Neurosciences Et de L'appareil Locomoteur, CRC-SEP, Hôpital Roger Salengro, Université de Lille, Inserm U1172, Lille, France.

Thibault Moreau (T)

Service de Neurologie, CHU de Dijon, Dijon, France.

Christine Lebrun-Frenay (C)

Service de Neurologie, Neurologie Pasteur 2, CHU de Nice, Université Nice Cote d'Azur UR2CA-URRIS, Nice, France.

Elisabeth Maillart (E)

Département de Neurologie, APHP, Hôpital Pitié-Salpêtrière, Paris, France.

Gilles Edan (G)

Service de Neurologie, CHU Pontchaillou, Rennes, France.

Jean-Philippe Neau (JP)

Service de Neurologie, CHU La Milétrie, Poitiers, France.

Alexis Montcuquet (A)

Service de Neurologie, CHU de Limoges, Limoges, France.

Philippe Cabre (P)

Service de Neurologie, CHU de Fort de France, Fort de France, France.

Jean-Philippe Camdessanché (JP)

Service de Neurologie, Hôpital Nord, CHU Saint-Étienne, Saint-Etienne, France.

Gilles Defer (G)

Service de Neurologie, Centre Expert SEP, CHU de Caen, Université Normandie, Caen, France.

Haifa Ben Nasr (HB)

Service de Neurologie, Hôpital Sud Francilien, Corbeil Essonnes, France.

Aude Maurousset (A)

Service de Neurologie, CHU Bretonneau, Tours, France.

Karolina Hankiewicz (K)

Service de Neurologie, CH de Saint-Denis, Saint-Denis, France.

Corinne Pottier (C)

Service de Neurologie, Hôpital René Dubos, Pontoise, France.

Emmanuelle Leray (E)

Université de Rennes/EHESP, REPERES - EA, 7449, Rennes, France.
CHU Rennes, CIC-P 1414, Rennes, France.

Sandra Vukusic (S)

Université de Lyon, Université Claude Bernard, Lyon 1, Lyon, France.
Service de Neurologie, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, sclérose en plaques, pathologies de la myéline et neuro-inflammation, Bron, France.
Centre de Recherche en Neurosciences de Lyon, Observatoire Français de La Sclérose en Plaques, INSERM 1028 et CNRS UMR 5292, Lyon, France.
EUGENE DEVIC EDMUS Foundation Against Multiple Sclerosis, State-Approved Foundation, Bron, France.

David-Axel Laplaud (DA)

Service de Neurologie, CHU Nantes, Nantes, France. david.laplaud@univ-nantes.fr.
INSERM, CIC 0004, CRTI-INSERM UMR U1064, Nantes, France. david.laplaud@univ-nantes.fr.

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Classifications MeSH