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Updated: Jun 17, 2026

Isolation, Enrichment, and Maintenance of Medulloblastoma Stem Cells
Published on: September 2, 2010
Treatment of early childhood medulloblastoma by postoperative chemotherapy alone
Stefan Rutkowski1, Udo Bode, Frank Deinlein
1Department of Pediatric Oncology, Children's Hospital, University of Würzburg, Würzburg, Germany. rutkowski@mail.uni-wuerzburg.de
Background:
The prognosis for young children with medulloblastoma is poor, and survivors are at high risk for cognitive deficits. We conducted a trial of the treatment of this brain tumor by intensive postoperative chemotherapy alone.
Methods:
After surgery, children received three cycles of intravenous chemotherapy (cyclophosphamide, vincristine, methotrexate, carboplatin, and etoposide) and intraventricular methotrexate. Treatment was terminated if a complete remission was achieved. Leukoencephalopathy and cognitive deficits were evaluated.
Results:
Forty-three children were treated according to protocol. In children who had complete resection (17 patients), residual tumor (14), and macroscopic metastases (12), the five-year progression-free and overall survival rates (+/-SE) were 82+/-9 percent and 93+/-6 percent, 50+/-13 percent and 56+/-14 percent, and 33+/-14 percent and 38+/-15 percent, respectively. The rates in 31 patients without macroscopic metastases were 68+/-8 percent and 77+/-8 percent. Desmoplastic histology, metastatic disease, and an age younger than two years were independent prognostic factors for tumor relapse and survival. Treatment strategies at relapse were successful in 8 of 16 patients. There were no major instances of unexpected toxicity. In 19 of 23 children, asymptomatic leukoencephalopathy was detected by magnetic resonance imaging. After treatment, the mean IQ was significantly lower than that of healthy controls within the same age group but higher than that of patients in a previous trial who had received radiotherapy.
Conclusions:
Postoperative chemotherapy alone is a promising treatment for medulloblastoma in young children without metastases.
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