Ongoing Response in a Multiply Relapsed Metastatic Posterior Fossa Ependymoma A After Vorinostat and Concomitant Irradiation

J Pediatr Hematol Oncol. 2022 Mar 1;44(2):e576-e579. doi: 10.1097/MPH.0000000000002175.

Abstract

Posterior fossa ependymomas A confer the worst prognosis among all subtypes. They demonstrate distinct epigenetic changes, which can be targeted with epigenetic modifiers like histone deacetylase inhibitors (Vorinostat). We describe a 3-year-old male diagnosed with a posterior fossa ependymoma who had a number of recurrences requiring multimodal therapy. Molecular analysis demonstrated a BCL-6 corepressor mutation, and methylation profiling matched with posterior fossa ependymomas A. He received craniospinal irradiation and focal boost with Vorinostat. Serial imaging after irradiation revealed a progressively decreasing tumor burden with nearly complete resolution of disease at 15 months. Histone deacetylase inhibitors demonstrate promise in treatment of carefully selected cases of ependymoma.

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Combined Modality Therapy
  • Ependymoma* / genetics
  • Ependymoma* / pathology
  • Ependymoma* / therapy
  • Histone Deacetylase Inhibitors*
  • Humans
  • Male
  • Vorinostat / therapeutic use

Substances

  • Histone Deacetylase Inhibitors
  • Vorinostat

Supplementary concepts

  • Familial ependymoma