Brain and Central Nervous System Tumors Clinical Trial
Official title:
A Phase II Study of Temozolomide in the Treatment of Children With High Grade Glioma
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing
so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor
cells. Giving chemotherapy together with radiation therapy may kill more tumor cells.
PURPOSE: This phase II trial is studying how well giving chemotherapy together with
radiation therapy after surgery followed by chemotherapy alone works in children with newly
diagnosed astrocytoma, glioblastoma multiforme, gliosarcoma, or diffuse intrinsic pontine
glioma.
OBJECTIVES:
- Compare the event-free survival of patients with newly diagnosed anaplastic
astrocytoma, glioblastoma multiforme, gliosarcoma, or diffuse intrinsic pontine glioma
(DIPG) treated with adjuvant temozolomide administered concurrently with postoperative
radiotherapy and then alone as maintenance therapy vs historical control cohorts
treated in prior Pediatric Oncology Group and Children's Cancer Group studies.
- Determine the toxicity of this regimen in these patients.
- Determine the efficacy of this regimen in patients with DIPG.
- Determine the toxicity of this regimen in patients with DIPG.
OUTLINE: This is a multicenter study.
- Adjuvant chemoradiotherapy: Beginning within 6 weeks after surgical resection or
diagnosis*, patients without gross residual disease undergo cranial irradiation 5 days
a week for 6 weeks. Beginning within 6 weeks after surgical resection, patients with
gross residual disease undergo radiotherapy as above followed by boost radiotherapy for
1 week. All patients receive oral temozolomide once daily beginning within 5 days after
initiation of radiotherapy and continuing for a total of 6 weeks in the absence of
disease progression or unacceptable toxicity.
- Adjuvant maintenance therapy: Beginning 4 weeks after completion of adjuvant
chemoradiotherapy, patients receive oral temozolomide on days 1-5. Treatment repeats
every 28 days for a total of 10 courses in the absence of disease progression or
unacceptable toxicity.
NOTE: *For patients with diffuse intrinsic pontine glioma only
Patients are followed every 3-6 months for 4 years and then annually thereafter.
PROJECTED ACCRUAL: A total of 50-60 patients will be accrued for this study within 12-14
months.
;
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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