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

Author:

Benallegue Nail12,Rollot Fabien3456,Wiertlewski Sandrine27,Casey Romain3456,Debouverie Marc8,Kerbrat Anne9,De Seze Jérôme10,Ciron Jonathan1112,Ruet Aurelie1314,Labauge Pierre15,Maillart Elisabeth16,Zephir Helene17,Papeix Caroline18,Defer Gilles19,Lebrun-Frenay Christine20,Moreau Thibault21,Berger Eric22,Stankoff Bruno23,Clavelou Pierre24,Heinzlef Olivier25,Pelletier Jean26,Thouvenot Eric2728,Al Khedr Abdullatif29,Bourre Bertrand30,Casez Olivier31,Cabre Philippe32,Wahab Abir33,Magy Laurent34,Vukusic Sandra3456,Laplaud David-Axel27, ,François Cotton35,Pascal Douek35,Alexandre Pachot35,Javier Olaiz35,Claire Rigaud-Bully35,Romain Marignier35,Emmanuelle Le Page35,Nicolas Collongues35,Mikaël Cohen35,Agnès Fromont35,Bertrand Audoin35,Claire Giannesini35,Olivier Gout35,Jean-Philippe Camdessanché35,Solène Moulin35,Ines Doghri35,Haifa Ben Nasr35,Karolina Hankiewicz35,Corinne Pottier35,Jean-Philippe Neau35,Céline Labeyrie35,Chantal Nifle35

Affiliation:

1. Department of Paediatric Neurology, Universitaire Angers, CHU Angers, Angers, France

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

3. Université de Lyon, Université Claude Bernard, Lyon 1, Lyon, France

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

5. Centre de Recherche en Neurosciences de Lyon, Observatoire Français de La Sclérose en Plaques, Inserm 1028 et CNRS UMR 5292, Lyon, France

6. EUGENE DEVIC EDMUS Foundation Against Multiple Sclerosis, State-Approved Foundation, Bron, France

7. Department of Neurology, CHU Nantes, Nantes, France

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

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

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

11. Department of Neurology, CRC-SEP, CHU de Toulouse, Hôpital Pierre-Paul Riquet, Toulouse, France

12. Institut Toulousain Des Maladies Infectieuses Et Inflammatoires (Infinity), Inserm UMR 1291, CNRS UMR 5051, Université Toulouse III, Toulouse, France

13. Department of Neurology, CHU de Bordeaux, Bordeaux, France

14. Université de Bordeaux, Inserm, Neurocentre Magendie, U1215 Bordeaux, France

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

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

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

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

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

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

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

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

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

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

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

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

27. Department of Neurology, CHU de Nîmes, Nîmes, France

28. IGF, University Montpellier, CNRS, Inserm, Montpellier, France

29. Department of Neurology, CHU d’Amiens, Amiens, France

30. CHU Rouen, Rouen, France

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

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

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

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

35. for the OFSEP (Observatoire Français de la Sclérose en Plaques) Investigators

Abstract

ImportanceModerately 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.ObjectiveTo assess the real-world association of HET as an index treatment compared with MET with disease activity.Design, Setting, and ParticipantsThis 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.ExposureHET or MET at treatment initiation.Main Outcomes and MeasuresThe 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.ResultsOf 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 RelevanceResults 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.

Publisher

American Medical Association (AMA)

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