TREATMENT READING
Childhood Central Nervous System Atypical Teratoid/Rhabdoid Tumor
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Selected text from the National Cancer Institute, with original links and dates. This Triangle reading page is not an NCI PDQ summary. Source topics may be broader than an individual diagnosis.
3 studies cited in this topic · see design and results →
Explore 2 related disease and treatment settings → · Source-derived catalogue; clinical review pending.
Certain factors affect prognosis (chance of recovery) and treatment options.
Treatment Option Overview
Key Points
There are different types of treatment for children with central nervous system (CNS) atypical teratoid/rhabdoid tumor (AT/RT).
Children with AT/RT should have their treatment planned by a team of health care providers who are experts in treating cancer in children.
Childhood brain tumors may cause symptoms that begin before the cancer is diagnosed and continue for months or years.
The following types of treatment may be used:
Surgery
Chemotherapy
Radiation therapy
Stem cell transplant
Clinical trials
Treatment for childhood CNS AT/RT may cause side effects.
Follow-up care may be needed.
Resources and support are available to help you cope with your child's cancer.
Treatment of Childhood Central Nervous System Atypical Teratoid/Rhabdoid Tumor
Treatment of Recurrent Childhood Central Nervous System Atypical Teratoid/Rhabdoid Tumor
Preserved source evidence · Independent clinical review pending · Not medical advice
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