Two-year follow-up during fingolimod treatment in a pediatric multiple sclerosis patient still active on first-line treatment

Neurol Sci. 2021 May;42(Suppl 1):15-18. doi: 10.1007/s10072-021-05058-9. Epub 2021 Jan 19.

Abstract

Treatment of pediatric multiple sclerosis (MS) has been increasingly debated in the last few years due to limited knowledge of treatment strategies and therapeutic options. When MS develops at a young age, it usually has a very inflammatory disease course, with many relapses and disease activity as seen in magnetic resonance imaging (MRI). Therefore, treatment with immunomodulatory drugs may be beneficial in these patients. However, limited data are available to date on the treatment of pediatric MS. Although observational, prospective, and retrospective studies provide some information on its treatment course, only one clinical trial in pediatric patients has been published, the PARADIGMS trial, which showed an 82% reduction in relapse rate with fingolimod (0.5 mg/day) versus interferon β-1a (30 μg once weekly intramuscularly). Here, we present the case of a pediatric patient with MS (age of onset, 13 years), who was initially treated with interferon β-1a for 2 years and subsequently switched to fingolimod, owing to clinical and radiological activity despite treatment with interferon β-1a.

Keywords: Fingolimod; Interferon β-1a; Pediatric multiple sclerosis; Treatment strategies.

MeSH terms

  • Adolescent
  • Child
  • Fingolimod Hydrochloride / therapeutic use
  • Follow-Up Studies
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Interferon beta-1a / therapeutic use
  • Multiple Sclerosis* / diagnostic imaging
  • Multiple Sclerosis* / drug therapy
  • Multiple Sclerosis, Relapsing-Remitting* / diagnostic imaging
  • Multiple Sclerosis, Relapsing-Remitting* / drug therapy
  • Prospective Studies
  • Retrospective Studies

Substances

  • Immunosuppressive Agents
  • Fingolimod Hydrochloride
  • Interferon beta-1a