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Highly Effective Therapies as First-Line Treatment for Pediatric-Onset Multiple Sclerosis.
Benallegue, Nail; Rollot, Fabien; Wiertlewski, Sandrine; Casey, Romain; Debouverie, Marc; Kerbrat, Anne; De Seze, Jérôme; Ciron, Jonathan; Ruet, Aurelie; Labauge, Pierre; Maillart, Elisabeth; Zephir, Helene; Papeix, Caroline; Defer, Gilles; Lebrun-Frenay, Christine; Moreau, Thibault; Berger, Eric; Stankoff, Bruno; Clavelou, Pierre; Heinzlef, Olivier; Pelletier, Jean; Thouvenot, Eric; Al Khedr, Abdullatif; Bourre, Bertrand; Casez, Olivier; Cabre, Philippe; Wahab, Abir; Magy, Laurent; Vukusic, Sandra; Laplaud, David-Axel.
Afiliación
  • Benallegue N; Department of Paediatric Neurology, Universitaire Angers, CHU Angers, Angers, France.
  • Rollot F; Nantes Université, CHU Nantes, Inserm, CIC 14131413, Center for Research in Transplantation and Translational Immunology, UMR 1064, Nantes, France.
  • Wiertlewski S; Université de Lyon, Université Claude Bernard, Lyon 1, Lyon, France.
  • Casey R; Department of Neurology, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, Sclérose en Plaques, Pathologies de la Myéline et Neuro-Infammation, Bron, France.
  • Debouverie M; Centre de Recherche en Neurosciences de Lyon, Observatoire Français de La Sclérose en Plaques, Inserm 1028 et CNRS UMR 5292, Lyon, France.
  • Kerbrat A; EUGENE DEVIC EDMUS Foundation Against Multiple Sclerosis, State-Approved Foundation, Bron, France.
  • De Seze J; Nantes Université, CHU Nantes, Inserm, CIC 14131413, Center for Research in Transplantation and Translational Immunology, UMR 1064, Nantes, France.
  • Ciron J; Department of Neurology, CHU Nantes, Nantes, France.
  • Ruet A; Université de Lyon, Université Claude Bernard, Lyon 1, Lyon, France.
  • Labauge P; Department of Neurology, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, Sclérose en Plaques, Pathologies de la Myéline et Neuro-Infammation, Bron, France.
  • Maillart E; Centre de Recherche en Neurosciences de Lyon, Observatoire Français de La Sclérose en Plaques, Inserm 1028 et CNRS UMR 5292, Lyon, France.
  • Zephir H; EUGENE DEVIC EDMUS Foundation Against Multiple Sclerosis, State-Approved Foundation, Bron, France.
  • Papeix C; Department of Neurology, Centre Hospitalier Régional Et Universitaire de Nancy, Université de Lorraine, 4360 APEMAC Vandoeuvre-Lès-Nancy, EA, France.
  • Defer G; Rennes University, CHU Rennes, CRC-SEP Neurology Department, and EMPENN U 1228, Inserm, INRIA, CNRS, Rennes, France.
  • Lebrun-Frenay C; Department of Neurology Et Centre d'Investigation Clinique, CHU de Strasbourg, INSERM 1434, Strasbourg, France.
  • Moreau T; Department of Neurology, CRC-SEP, CHU de Toulouse, Hôpital Pierre-Paul Riquet, Toulouse, France.
  • Berger E; Institut Toulousain Des Maladies Infectieuses Et Inflammatoires (Infinity), Inserm UMR 1291, CNRS UMR 5051, Université Toulouse III, Toulouse, France.
  • Stankoff B; Department of Neurology, CHU de Bordeaux, Bordeaux, France.
  • Clavelou P; Université de Bordeaux, Inserm, Neurocentre Magendie, U1215 Bordeaux, France.
  • Heinzlef O; CRC SEP, Department of Neurology, Montpellier Universitary Hospital, Montpellier, France.
  • Pelletier J; Department of Neurology, APHP, Hôpital Pitié-Salpêtrière, Paris, France.
  • Thouvenot E; Pôle Des Neurosciences Et de L'appareil Locomoteur, CRC-SEP, Hôpital Roger Salengro, Université de Lille, Inserm U1172, Lille, France.
  • Al Khedr A; Département of Neurology, Hôpital Fondation A.de Rothschild, Paris, France.
  • Bourre B; Department of Neurology, Centre Expert SEP, CHU de Caen, Université Normandie, Caen, France.
  • Casez O; CRC-SEP Neurologie Pasteur 2, CHU de Nice, Université Cote d'Azur, UMR2CA (URRIS), Nice, France.
  • Cabre P; Department of Neurology, CHU de Dijon, Dijon, France.
  • Wahab A; Department of Neurology, CHU de Besançon, Besançon, France.
  • Magy L; Department of Neurology, CHU Saint-Antoine, Paris, France.
  • Vukusic S; Department of Neurology, CHU de Clermont-Ferrand, Clermont-Ferrand, France.
  • Laplaud DA; Département de Neurologie, Centre Hospitalier de Poissy, St Germain, France.
JAMA Neurol ; 81(3): 273-282, 2024 Mar 01.
Article en En | MEDLINE | ID: mdl-38345791
ABSTRACT
Importance Moderately effective therapies (METs) have been the main treatment in pediatric-onset multiple sclerosis (POMS) for years. Despite the expanding use of highly effective therapies (HETs), treatment strategies for POMS still lack consensus.

Objective:

To assess the real-world association of HET as an index treatment compared with MET with disease activity. Design, Setting, and

Participants:

This was a retrospective cohort study conducted from January 1, 2010, to December 8, 2022, until the last recorded visit. The median follow-up was 5.8 years. A total of 36 French MS centers participated in the Observatoire Français de la Sclérose en Plaques (OFSEP) cohort. Of the total participants in OFSEP, only treatment-naive children with relapsing-remitting POMS who received a first HET or MET before adulthood and at least 1 follow-up clinical visit were included in the study. All eligible participants were included in the study, and none declined to participate. Exposure HET or MET at treatment initiation. Main Outcomes and

Measures:

The primary outcome was the time to first relapse after treatment. Secondary outcomes were annualized relapse rate (ARR), magnetic resonance imaging (MRI) activity, time to Expanded Disability Status Scale (EDSS) progression, tertiary education attainment, and treatment safety/tolerability. An adapted statistical method was used to model the logarithm of event rate by penalized splines of time, allowing adjustment for effects of covariates that is sensitive to nonlinearity and interactions.

Results:

Of the 3841 children (5.2% of 74 367 total participants in OFSEP), 530 patients (mean [SD] age, 16.0 [1.8] years; 364 female [68.7%]) were included in the study. In study patients, both treatment strategies were associated with a reduced risk of first relapse within the first 2 years. HET dampened disease activity with a 54% reduction in first relapse risk (adjusted hazard ratio [HR], 0.46; 95% CI, 0.31-0.67; P < .001) sustained over 5 years, confirmed on MRI activity (adjusted odds ratio [OR], 0.34; 95% CI, 0.18-0.66; P = .001), and with a better tolerability pattern than MET. The risk of discontinuation at 2 years was 6 times higher with MET (HR, 5.97; 95% CI, 2.92-12.20). The primary reasons for treatment discontinuation were lack of efficacy and intolerance. Index treatment was not associated with EDSS progression or tertiary education attainment (adjusted OR, 0.51; 95% CI, 0.24-1.10; P = .09). Conclusions and Relevance Results of this cohort study suggest that compared with MET, initial HET in POMS was associated with a reduction in the risk of first relapse with an optimal outcome within the first 2 years and was associated with a lower rate of treatment switching and a better midterm tolerance in children. These findings suggest prioritizing initial HET in POMS, although long-term safety studies are needed.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esclerosis Múltiple Recurrente-Remitente / Esclerosis Múltiple Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Female / Humans Idioma: En Revista: JAMA Neurol Año: 2024 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esclerosis Múltiple Recurrente-Remitente / Esclerosis Múltiple Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Female / Humans Idioma: En Revista: JAMA Neurol Año: 2024 Tipo del documento: Article País de afiliación: Francia