Brain Tumors Clinical Trial
Official title:
Study Of Reduced Dose Craniospinal Radiotherapy (1800 cGy) And Chemotherapy In Children With Newly-Diagnosed Standard-Risk Posterior Fossa Primitive Neuro-ectodermal Tumor (PNET/Medulloblastoma)
RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells, but also damages normal cells in the developing brains of children. Combining low-dose radiation therapy in combination with chemotherapy should be effective in treating medulloblastoma while avoiding the long-term side effects of giving higher dose radiation to children with newly diagnosed average risk medulloblastoma.
OBJECTIVES:
- By giving reduced dose craniospinal radiation followed by nine cycles of maintenance
chemotherapy comprised of alternating cycles of lomustine, cisplatin, and vincristine
alternating with cyclophosphamide and etoposide, we will reduce the late effects of
higher dose radiation in children while maintaining the therapeutic efficacy (86% 3-year
relapse-free survival) of current standard therapy
- To evaluate the late neurotoxic effects of low-dose craniospinal radiotherapy, in terms
of cognitive, endocrinologic, and auditory function, in these patients.
OUTLINE: This is a multi center study of reduced dose craniospinal radiotherapy and
chemotherapy in patients ages 3 - 30 years with newly diagnosed average risk medulloblastoma.
- Induction chemoradiotherapy: Beginning within 28 days after complete surgical resection,
patients undergo radiotherapy to the craniospinal axis (1800 centigray (cGy)) followed
by conformal radiotherapy to the tumor bed (5400 cGy). Patients receive vincristine
weekly for 6 weeks.
- Maintenance chemotherapy: Beginning 4 weeks after the completion of craniospinal
radiation therapy, patients receive two 6-week courses of regimen A as outlined below
alternating with one 6-week course of regimen B for a total of 9 courses (AABAABAAB).
- Regimen A: Patients receive oral lomustine and cisplatin on day 0 and vincristine
on days 0, 7, and 14.
- Regimen B: Patients receive cyclophosphamide on days 0 and 1 and etoposide
intravenous (IV) on days 0 and 1, followed by oral etoposide on days 14-34.
Patients are followed every 3 months for 1 year, every 6 months for 2 years, and then
annually thereafter with surveillance neuroimaging using Magnetic Resonance Imaging Scan (MRI
scan) and clinical examination.
PROJECTED ACCRUAL: A total of 50 patients will be accrued for this study within 3 years.
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