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PET and MRI Guided Irradiation of a Glioblastoma Rat Model Using a Micro-irradiator
Published on: December 28, 2017
Insights
Radiotherapy for pediatric brain tumors shows variable outcomes. While some tumors have a good prognosis, others are associated with poor survival rates, with at least 4000 rad needed for tumor control.
Area of Science:
- Pediatric Oncology
- Radiation Oncology
- Neuro-oncology
Background:
- Primary intracranial tumors are a significant concern in children under five years old.
- Radiotherapy is a primary treatment modality for these tumors.
Purpose of the Study:
- To evaluate the efficacy of radiotherapy in treating primary intracranial tumors in young children.
- To identify prognostic factors influencing survival rates and long-term outcomes.
Main Methods:
- Retrospective analysis of 91 children under five years treated with radiotherapy for primary intracranial tumors.
- Correlation of tumor type, location, dose, age at diagnosis, and survival rates.
- Assessment of long-term survival and quality of life in survivors.
Main Results:
- Cerebellar astrocytomas and optic chiasm gliomas showed favorable outcomes.
- Brain stem tumors, extensive posterior fossa tumors, and cerebral gliomas had poor prognoses.
- Medulloblastomas, ependymomas, and midbrain tumors had intermediate prognoses.
- A minimum tumor dose of 4000 rad appeared necessary for tumor control.
- Of 63 children diagnosed over five years prior, 43% survived at least five years.
- Most long-term survivors lead normal lives with some mild impairments.
Conclusions:
- Radiotherapy outcomes for pediatric intracranial tumors vary significantly by tumor type and location.
- Age at diagnosis showed a minor correlation with survival, with older children (>24 months) faring slightly better.
- Effective tumor control requires doses of at least 4000 rad, and long-term survivors generally have good quality of life.
Abstract:
Ninety-one children younger than age five years have been treated with radiotherapy for primary intracranial tumors. Patients with cerebellar astrocytomas and optic chiasm gliomas did relatively well, whereas brain stem tumors, extensive posterior fossa tumors and cerebral gliomas had a poor prognosis. Medulloblastomas, ependymomas, and midbrain tumors were of intermediate prognosis. There was no definite correlation between age at diagnosis and survival, although patients over 24 months of age seemed to do slightly better. Tumor doses of at least 4000 rad seem necessary for any likelihood of control. Of 63 children diagnosed over five years ago, 27 (43%) survived at least five years. The majority of long-term survivors are leading normal lives, although many have mild impairments.

