<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>81(3)</volume><submitter>Benallegue N</submitter><pubmed_abstract>&lt;h4>Importance&lt;/h4>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.&lt;h4>Objective&lt;/h4>To assess the real-world association of HET as an index treatment compared with MET with disease activity.&lt;h4>Design, setting, and participants&lt;/h4>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 rec</pubmed_abstract><journal>JAMA neurology</journal><pagination>273-282</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10862269</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Highly Effective Therapies as First-Line Treatment for Pediatric-Onset Multiple Sclerosis.</pubmed_title><pmcid>PMC10862269</pmcid><pubmed_authors>Labauge P</pubmed_authors><pubmed_authors>Kerbrat A</pubmed_authors><pubmed_authors>Heinzlef O</pubmed_authors><pubmed_authors>Debouverie M</pubmed_authors><pubmed_authors>Rollot F</pubmed_authors><pubmed_authors>Olivier G</pubmed_authors><pubmed_authors>Moreau T</pubmed_authors><pubmed_authors>Casez O</pubmed_authors><pubmed_authors>Vukusic S</pubmed_authors><pubmed_authors>Francois C</pubmed_authors><pubmed_authors>Claire G</pubmed_authors><pubmed_authors>Wiertlewski S</pubmed_authors><pubmed_authors>Zephir H</pubmed_authors><pubmed_authors>Ciron J</pubmed_authors><pubmed_authors>Thouvenot E</pubmed_authors><pubmed_authors>Papeix C</pubmed_authors><pubmed_authors>Cabre P</pubmed_authors><pubmed_authors>Celine L</pubmed_authors><pubmed_authors>Maillart E</pubmed_authors><pubmed_authors>Claire RB</pubmed_authors><pubmed_authors>Berger E</pubmed_authors><pubmed_authors>Al Khedr A</pubmed_authors><pubmed_authors>Bertrand A</pubmed_authors><pubmed_authors>Pelletier J</pubmed_authors><pubmed_authors>Corinne P</pubmed_authors><pubmed_authors>Clavelou P</pubmed_authors><pubmed_authors>Defer G</pubmed_authors><pubmed_authors>Alexandre P</pubmed_authors><pubmed_authors>Magy L</pubmed_authors><pubmed_authors>Chantal N</pubmed_authors><pubmed_authors>Romain M</pubmed_authors><pubmed_authors>Stankoff B</pubmed_authors><pubmed_authors>Javier O</pubmed_authors><pubmed_authors>Pascal D</pubmed_authors><pubmed_authors>Agnes F</pubmed_authors><pubmed_authors>Jean-Philippe N</pubmed_authors><pubmed_authors>Casey R</pubmed_authors><pubmed_authors>De Seze J</pubmed_authors><pubmed_authors>OFSEP (Observatoire Français de la Sclérose en Plaques) Investigators</pubmed_authors><pubmed_authors>Ines D</pubmed_authors><pubmed_authors>Mikael C</pubmed_authors><pubmed_authors>Karolina H</pubmed_authors><pubmed_authors>Bourre B</pubmed_authors><pubmed_authors>Nicolas C</pubmed_authors><pubmed_authors>Haifa BN</pubmed_authors><pubmed_authors>Benallegue N</pubmed_authors><pubmed_authors>Lebrun-Frenay C</pubmed_authors><pubmed_authors>Wahab A</pubmed_authors><pubmed_authors>Solene M</pubmed_authors><pubmed_authors>Laplaud DA</pubmed_authors><pubmed_authors>Emmanuelle LP</pubmed_authors><pubmed_authors>Jean-Philippe C</pubmed_authors><pubmed_authors>Ruet A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Highly Effective Therapies as First-Line Treatment for Pediatric-Onset Multiple Sclerosis.</name><description>&lt;h4>Importance&lt;/h4>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.&lt;h4>Objective&lt;/h4>To assess the real-world association of HET as an index treatment compared with MET with disease activity.&lt;h4>Design, setting, and participants&lt;/h4>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 rec</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-07-14T18:59:30.422Z</modification><creation>2025-04-07T08:59:00.033Z</creation></dates><accession>S-EPMC10862269</accession><cross_references><pubmed>38345791</pubmed><doi>10.1001/jamaneurol.2023.5566</doi></cross_references></HashMap>