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Comparative Effectiveness of Natalizumab Versus Anti-CD20 in Highly Active Relapsing-Remitting Multiple Sclerosis After Fingolimod Withdrawal.
Rollot, Fabien; Couturier, Justine; Casey, Romain; Wiertlewski, Sandrine; Debouverie, Marc; Pelletier, Jean; De Sèze, Jérôme; Labauge, Pierre; Ruet, Aurélie; Thouvenot, Eric; Ciron, Jonathan; Berger, Eric; Gout, Olivier; Clavelou, Pierre; Stankoff, Bruno; Casez, Olivier; Bourre, Bertrand; Zephir, Hélène; Moreau, Thibault; Lebrun-Frenay, Christine; Maillart, Elisabeth; Edan, Gilles; Neau, Jean-Philippe; Montcuquet, Alexis; Cabre, Philippe; Camdessanché, Jean-Philippe; Defer, Gilles; Nasr, Haifa Ben; Maurousset, Aude; Hankiewicz, Karolina; Pottier, Corinne; Leray, Emmanuelle; Vukusic, Sandra; Laplaud, David-Axel.
Afiliación
  • Rollot F; Université de Lyon, Université Claude Bernard, Lyon 1, Lyon, France. Fabien.rollot@chu-lyon.fr.
  • Couturier J; 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.
  • Casey R; 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.
  • Wiertlewski S; EUGENE DEVIC EDMUS Foundation Against Multiple Sclerosis, State-Approved Foundation, Bron, France. Fabien.rollot@chu-lyon.fr.
  • Debouverie M; Service de Neurologie, CHU Nantes, Nantes, France.
  • Pelletier J; Université de Lyon, Université Claude Bernard, Lyon 1, Lyon, France.
  • De Sèze J; Service de Neurologie, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, sclérose en plaques, pathologies de la myéline et neuro-inflammation, Bron, France.
  • Labauge P; Centre de Recherche en Neurosciences de Lyon, Observatoire Français de La Sclérose en Plaques, INSERM 1028 et CNRS UMR 5292, Lyon, France.
  • Ruet A; EUGENE DEVIC EDMUS Foundation Against Multiple Sclerosis, State-Approved Foundation, Bron, France.
  • Thouvenot E; Service de Neurologie, CHU Nantes, Nantes, France.
  • Ciron J; INSERM, CIC 0004, CRTI-INSERM UMR U1064, Nantes, France.
  • Berger E; Service de Neurologie, Centre Hospitalier Régional Et Universitaire de Nancy, Université de Lorraine, 4360 APEMAC, Vandoeuvre-Lès-Nancy, EA, France.
  • Gout O; Aix Marseille University, APHM, Hôpital de La Timone, Pôle de Neurosciences Cliniques, Service de Neurologie, CEMEREM, 13005, Marseille, France.
  • Clavelou P; Service de Neurologie Et Centre d'Investigation Clinique, CHU de Strasbourg, INSERM 1434, Strasbourg, France.
  • Stankoff B; Service de Neurologie, CHU de Montpellier, Montpellier, France.
  • Casez O; Service de Neurologie, CHU de Bordeaux, Bordeaux, France.
  • Bourre B; Université de Bordeaux, INSERM, Neurocentre Magendie, U1215, Bordeaux, France.
  • Zephir H; Service de Neurologie, CHU de Nîmes, Nîmes, France.
  • Moreau T; Institut de Génomique Fonctionnelle, Université de Montpellier, CNRS, INSERM, Montpellier, France.
  • Lebrun-Frenay C; Service de Neurologie, CHU de Toulouse, Hôpital Pierre-Paul Riquet, CRC-SEP, Toulouse, France.
  • Maillart E; Institut Toulousain Des Maladies Infectieuses Et Inflammatoires (Infinity), INSERM UMR 1291, CNRS UMR 5051, Université Toulouse III, Toulouse, France.
  • Edan G; Service de Neurologie, CHU de Besançon, Besançon, France.
  • Neau JP; Service de Neurologie, Hôpital Fondation A de Rothschild, Paris, France.
  • Montcuquet A; Service de Neurologie, CHU de Clermont-Ferrand, Clermont-Ferrand, France.
  • Cabre P; Service de Neurologie, CHU Saint-Antoine, Paris, France.
  • Camdessanché JP; Service de Neurologie, CHU de Grenoble, Grenoble, France.
  • Defer G; Service de Neurologie, CHU de Rouen, Rouen, France.
  • Nasr HB; Pôle Des Neurosciences Et de L'appareil Locomoteur, CRC-SEP, Hôpital Roger Salengro, Université de Lille, Inserm U1172, Lille, France.
  • Maurousset A; Service de Neurologie, CHU de Dijon, Dijon, France.
  • Hankiewicz K; Service de Neurologie, Neurologie Pasteur 2, CHU de Nice, Université Nice Cote d'Azur UR2CA-URRIS, Nice, France.
  • Pottier C; Département de Neurologie, APHP, Hôpital Pitié-Salpêtrière, Paris, France.
  • Leray E; Service de Neurologie, CHU Pontchaillou, Rennes, France.
  • Vukusic S; Service de Neurologie, CHU La Milétrie, Poitiers, France.
  • Laplaud DA; Service de Neurologie, CHU de Limoges, Limoges, France.
Neurotherapeutics ; 19(2): 476-490, 2022 03.
Article en En | MEDLINE | ID: mdl-35217934
ABSTRACT
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Esclerosis Múltiple Recurrente-Remitente / Esclerosis Múltiple Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Neurotherapeutics Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Esclerosis Múltiple Recurrente-Remitente / Esclerosis Múltiple Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Neurotherapeutics Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Francia