HEALTH PROFESSIONAL · SOURCE READING
Treatment Option Overview for Childhood CNS Germ Cell Tumors
Source: Childhood Central Nervous System Germ Cell Tumors Treatment (PDQ®)–Health Professional Version, National Cancer Institute.
Source updated: October 8, 2024 · Captured 2026-09-09.
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Teratomas, germinomas, and other nongerminomatous germ cell tumors (NGGCTs) have differing prognoses and require different treatment regimens. Studies have observed the following:[1-5]
For children older than 3 years and adults, radiation therapy has been an important component of therapy for germinomas and NGGCTs, although the optimal dose and field of irradiation are debated.
Central nervous system (CNS) germ cell tumors (GCTs), similar to gonadal and extragonadal GCTs, have demonstrated sensitivity to chemotherapy.
Germinomas are highly chemosensitive and radiosensitive tumors. They are curable with craniospinal irradiation and local site–boost radiation therapy alone. However, the use of neoadjuvant or preirradiation chemotherapy allows reduced radiation therapy doses and volumes and, subsequently, reduced long-term radiation therapy–related effects.
In North America and Europe, patients with localized germinomas are effectively treated with whole-ventricular irradiation supplemented with tumor site–boost radiation therapy. Focal irradiation to the tumor bed, regardless of response to chemotherapy, is considered inadequate treatment.[6]
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For NGGCTs, the combined use of more intensive neoadjuvant chemotherapy followed by either localized or craniospinal irradiation has resulted in improved survival rates in the last decade.[5,7,8]
Patients with bifocal intracranial GCTs limited to the suprasellar and pineal region were treated in the same manner as patients with localized, nonmetastatic tumors in studies in North America and Europe.[8]
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Table 3 outlines the treatment options for patients with newly diagnosed and recurrent childhood CNS GCTs.
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| Treatment Group | Treatment Options | |
|---|---|---|
| Newly diagnosed childhood CNS germinomas | Neoadjuvant chemotherapy followed by response-based radiation therapy | |
| Radiation therapy | ||
| Newly diagnosed childhood CNS nongerminomatous GCTs | Chemotherapy followed by radiation therapy | |
| Surgery, if incomplete response to chemotherapy before irradiation | ||
| Newly diagnosed childhood CNS teratomas | Gross-total resection | |
| Recurrent childhood CNS GCTs | Chemotherapy followed by additional radiation therapy | |
| High-dose chemotherapy with stem cell rescue with or without additional radiation therapy | ||
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- Neoadjuvant chemotherapy followed by response-based radiation therapy
- Radiation therapy
- Chemotherapy followed by radiation therapy
- Surgery, if incomplete response to chemotherapy before irradiation
- Gross-total resection
- Chemotherapy followed by additional radiation therapy
- High-dose chemotherapy with stem cell rescue with or without additional radiation therapy
Dramatic improvements in survival have been achieved for children and adolescents with cancer. Between 1975 and 2010, childhood cancer mortality decreased by more than 50%.[9] Childhood and adolescent cancer survivors require close monitoring because side effects of cancer therapy may persist or develop months or years after treatment. For information about the incidence, type, and monitoring of late effects in childhood and adolescent cancer survivors, see Late Effects of Treatment for Childhood Cancer.
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