A phase I trial of arsenic trioxide chemoradiotherapy for infiltrating astrocytomas of childhood

Neuro Oncol. 2013 Jun;15(6):783-7. doi: 10.1093/neuonc/not021. Epub 2013 Mar 3.

Abstract

Background: Arsenic trioxide (ATO) has demonstrated preclinical evidence of activity in the treatment of infiltrating astrocytomas.

Methods: We conducted a phase I trial of ATO given concomitantly with radiation therapy in children with newly diagnosed anaplastic astrocytoma, glioblastoma, or diffuse intrinsic pontine glioma. Eligible patients received a fixed daily dose of 0.15 mg/kg of ATO once a week, with each subsequent cohort of patients receiving an additional dose per week up to a planned frequency of ATO administration 5 days per week as tolerated. Twenty-four children were enrolled and 21 children were evaluable.

Results: ATO was well tolerated throughout the entire dose escalation, resulting in confirmation of safety when administered 5 days per week during irradiation.

Conclusions: The recommended dose of ATO during conventional irradiation is 0.15 mg/kg given on a daily basis with each fraction of radiation therapy administered.

Keywords: arsenic trioxide; astrocytoma; chemoradiotherapy; pediatrics.

Publication types

  • Clinical Trial, Phase I
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Antineoplastic Agents / therapeutic use
  • Arsenic Trioxide
  • Arsenicals / therapeutic use*
  • Astrocytoma / mortality
  • Astrocytoma / pathology
  • Astrocytoma / therapy*
  • Brain Stem Neoplasms / mortality
  • Brain Stem Neoplasms / pathology
  • Brain Stem Neoplasms / therapy*
  • Chemoradiotherapy*
  • Child
  • Child, Preschool
  • Dose Fractionation, Radiation
  • Female
  • Follow-Up Studies
  • Humans
  • Male
  • Neoplasm Grading
  • Oxides / therapeutic use*
  • Prognosis
  • Survival Rate
  • Young Adult

Substances

  • Antineoplastic Agents
  • Arsenicals
  • Oxides
  • Arsenic Trioxide