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← Childhood Central Nervous System Atypical Teratoid/Rhabdoid Tumor

FOR PATIENTS · SOURCE READING

Treatment of Childhood Central Nervous System Atypical Teratoid/Rhabdoid Tumor

Source: Childhood Central Nervous System Atypical Teratoid/Rhabdoid Tumor Treatment (PDQ®)–Patient Version, National Cancer Institute.

Source updated: December 19, 2024 · Captured 2026-09-09.

Selected source text with whitespace normalised. This Triangle page is not an NCI PDQ summary. Independent clinical review is pending.

For information about the treatments listed below, see the Treatment Option Overview section.

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There is no standard treatment for children with newly diagnosed central nervous system (CNS) atypical teratoid/rhabdoid tumor (AT/RT). Because AT/RT is fast-growing, a combination of treatments is usually given.

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After surgery to remove the tumor, treatment for AT/RT may include combinations of:

chemotherapy

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radiation therapy

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high-dose chemotherapy with stem cell transplant

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Use our clinical trial search to find NCI-supported cancer clinical trials that are accepting patients. You can search for trials based on the type of cancer, the age of the patient, and where the trials are being done. General information about clinical trials is also available.

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Preserved source evidence · Independent clinical review pending · Not medical advice