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

AbstractBACKGROUND:
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.
AuthorsKenneth J Cohen, Iris C Gibbs, Paul G Fisher, Robert J Hayashi, Margaret E Macy, Lia Gore
JournalNeuro-oncology (Neuro Oncol) Vol. 15 Issue 6 Pg. 783-7 (Jun 2013) ISSN: 1523-5866 [Electronic] England
PMID23460318 (Publication Type: Clinical Trial, Phase I, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Arsenicals
  • Oxides
  • Arsenic Trioxide
Topics
  • Adolescent
  • Adult
  • Antineoplastic Agents (therapeutic use)
  • Arsenic Trioxide
  • Arsenicals (therapeutic use)
  • Astrocytoma (mortality, pathology, therapy)
  • Brain Stem Neoplasms (mortality, pathology, therapy)
  • Chemoradiotherapy
  • Child
  • Child, Preschool
  • Dose Fractionation, Radiation
  • Female
  • Follow-Up Studies
  • Humans
  • Male
  • Neoplasm Grading
  • Oxides (therapeutic use)
  • Prognosis
  • Survival Rate
  • Young Adult

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