Clinical Trials Directory

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UnknownNCT00281905

Combination Chemotherapy With or Without Radiation Therapy in Treating Children With Brain Tumors

Management of Children Aged Less Than 3 Years With Brain Tumors

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Children's Cancer and Leukaemia Group · Academic / Other
Sex
All
Age
3 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving radiation therapy after chemotherapy may kill any remaining tumor cells. PURPOSE: This phase II trial is studying how well giving combination chemotherapy together with or without radiation therapy works in treating children with brain tumors.

Detailed description

OBJECTIVES: * Determine the response rate in children under 36 months of age with primary brain or brain stem tumors treated with vincristine, methotrexate, carboplatin, cyclophosphamide, and cisplatin with or without radiotherapy. * Determine the event-free survival and overall survival in children treated with this regimen. * Determine the pattern of local recurrence or occurrence of CNS metastases in children treated with this regimen. * Determine the quality of life in children treated with this regimen. * Determine the tolerability and long-term toxicity of this regimen in these children. * Determine the proportion of children who require radiotherapy after treatment with this regimen. * Determine the prognosis of children who receive both chemotherapy and radiotherapy. * Determine the nature and behavior of brain tumors in very young children. OUTLINE: This is a multicenter study. * Chemotherapy: Patients receive vincristine IV on days 0, 14, and 28; carboplatin IV over 4 hours on day 0; methotrexate IV continuously over 24 hours on day 14; cyclophosphamide IV over 4 hours on day 28; and cisplatin IV continuously over 48 hours on days 42 and 43. Courses repeat every 56 days (8 weeks) for up to 12 months. Patients who achieve a complete response proceed to observation, as do those achieving a partial response with no tumor present on biopsy. Patients with biopsy proven residual tumors after 12 months of chemotherapy or recurrent tumors that don't have the potential to spread through the cerebrospinal fluid (CSF) proceed to local radiotherapy. Patients with unresponsive disease or progressive disease that has the potential to spread through the CSF proceed to craniospinal radiotherapy. * Local radiotherapy: Patients undergo local radiotherapy 5 days a week for 5-5½ weeks. * Craniospinal radiotherapy: Patients undergo craniospinal radiotherapy 5 days a week for 4 weeks. Quality of life is assessed periodically. After completion of study treatment, patients are followed periodically for at least 2 years. PROJECTED ACCRUAL: A total of 50 patients will be accrued for this study.

Conditions

Interventions

TypeNameDescription
DRUGcarboplatin
DRUGcisplatin
DRUGcyclophosphamide
DRUGmethotrexate
DRUGvincristine sulfate
RADIATIONradiation therapy

Timeline

Start date
1992-06-01
First posted
2006-01-25
Last updated
2013-09-20

Locations

21 sites across 2 countries: Ireland, United Kingdom

Source: ClinicalTrials.gov record NCT00281905. Inclusion in this directory is not an endorsement.