Highly Effective Therapies as First-Line Treatment for Pediatric-Onset Multiple Sclerosis.


Journal

JAMA neurology
ISSN: 2168-6157
Titre abrégé: JAMA Neurol
Pays: United States
ID NLM: 101589536

Informations de publication

Date de publication:
12 Feb 2024
Historique:
medline: 12 2 2024
pubmed: 12 2 2024
entrez: 12 2 2024
Statut: aheadofprint

Résumé

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. To assess the real-world association of HET as an index treatment compared with MET with disease activity. 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. HET or MET at treatment initiation. 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. 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). 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.

Identifiants

pubmed: 38345791
pii: 2814784
doi: 10.1001/jamaneurol.2023.5566
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Investigateurs

Cotton François (C)
Douek Pascal (D)
Pachot Alexandre (P)
Olaiz Javier (O)
Rigaud-Bully Claire (RB)
Marignier Romain (M)
Le Page Emmanuelle (LP)
Collongues Nicolas (C)
Cohen Mikaël (C)
Fromont Agnès (F)
Audoin Bertrand (A)
Giannesini Claire (G)
Gout Olivier (G)
Camdessanché Jean-Philippe (C)
Moulin Solène (M)
Doghri Ines (D)
Ben Nasr Haifa (BN)
Hankiewicz Karolina (H)
Pottier Corinne (P)
Neau Jean-Philippe (N)
Labeyrie Céline (L)
Nifle Chantal (N)

Auteurs

Nail Benallegue (N)

Department of Paediatric Neurology, Universitaire Angers, CHU Angers, Angers, France.
Nantes Université, CHU Nantes, Inserm, CIC 14131413, Center for Research in Transplantation and Translational Immunology, UMR 1064, Nantes, France.

Fabien Rollot (F)

Université de Lyon, Université Claude Bernard, Lyon 1, Lyon, France.
Department of Neurology, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, Sclérose en Plaques, Pathologies de la Myéline et Neuro-Infammation, 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)

Nantes Université, CHU Nantes, Inserm, CIC 14131413, Center for Research in Transplantation and Translational Immunology, UMR 1064, Nantes, France.
Department of Neurology, CHU Nantes, Nantes, France.

Romain Casey (R)

Université de Lyon, Université Claude Bernard, Lyon 1, Lyon, France.
Department of Neurology, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, Sclérose en Plaques, Pathologies de la Myéline et Neuro-Infammation, 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.

Marc Debouverie (M)

Department of Neurology, Centre Hospitalier Régional Et Universitaire de Nancy, Université de Lorraine, 4360 APEMAC Vandoeuvre-Lès-Nancy, EA, France.

Anne Kerbrat (A)

Rennes University, CHU Rennes, CRC-SEP Neurology Department, and EMPENN U 1228, Inserm, INRIA, CNRS, Rennes, France.

Jérôme De Seze (J)

Department of Neurology Et Centre d'Investigation Clinique, CHU de Strasbourg, INSERM 1434, Strasbourg, France.

Jonathan Ciron (J)

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

Aurelie Ruet (A)

Department of Neurology, CHU de Bordeaux, Bordeaux, France.
Université de Bordeaux, Inserm, Neurocentre Magendie, U1215 Bordeaux, France.

Pierre Labauge (P)

CRC SEP, Department of Neurology, Montpellier Universitary Hospital, Montpellier, France.

Elisabeth Maillart (E)

Department of Neurology, APHP, Hôpital Pitié-Salpêtrière, Paris, France.

Helene Zephir (H)

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

Caroline Papeix (C)

Département of Neurology, Hôpital Fondation A.de Rothschild, Paris, France.

Gilles Defer (G)

Department of Neurology, Centre Expert SEP, CHU de Caen, Université Normandie, Caen, France.

Christine Lebrun-Frenay (C)

CRC-SEP Neurologie Pasteur 2, CHU de Nice, Université Cote d'Azur, UMR2CA (URRIS), Nice, France.

Thibault Moreau (T)

Department of Neurology, CHU de Dijon, Dijon, France.

Eric Berger (E)

Department of Neurology, CHU de Besançon, Besançon, France.

Bruno Stankoff (B)

Department of Neurology, CHU Saint-Antoine, Paris, France.

Pierre Clavelou (P)

Department of Neurology, CHU de Clermont-Ferrand, Clermont-Ferrand, France.

Olivier Heinzlef (O)

Département de Neurologie, Centre Hospitalier de Poissy, St Germain, France.

Jean Pelletier (J)

Aix Marseille Univ, APHM, Hôpital de la Timone, Pôle de Neurosciences Cliniques, Service de Neurologie - MICeME, CRMBM CEMEREM UMR7339, Marseille, France.

Eric Thouvenot (E)

Department of Neurology, CHU de Nîmes, Nîmes, France.
IGF, University Montpellier, CNRS, Inserm, Montpellier, France.

Abdullatif Al Khedr (A)

Department of Neurology, CHU d'Amiens, Amiens, France.

Bertrand Bourre (B)

CHU Rouen, Rouen, France.

Olivier Casez (O)

Department of Neurology, CHU de Grenoble, Grenoble, France.

Philippe Cabre (P)

Department of Neurology, CHU de Fort de France, Fort de France, France.

Abir Wahab (A)

Department of Neurology, Assistance Publique des Hôpitaux de Paris, Hôpital Henri Mondor, Université Paris Est, Créteil, France.

Laurent Magy (L)

Department of Neurology, CHU de Limoges, Limoges, France.

Sandra Vukusic (S)

Université de Lyon, Université Claude Bernard, Lyon 1, Lyon, France.
Department of Neurology, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, Sclérose en Plaques, Pathologies de la Myéline et Neuro-Infammation, 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)

Nantes Université, CHU Nantes, Inserm, CIC 14131413, Center for Research in Transplantation and Translational Immunology, UMR 1064, Nantes, France.
Department of Neurology, CHU Nantes, Nantes, France.

Classifications MeSH