Turkish Neurosurgery · 2019 · 13 citations · 27 references
MedicineOncologySurgeryChemotherapyPediatric OncologySurgical OncologyBrain TumorsPediatric Brain TumorsPediatric Neuro-oncologyPediatric Neurosurgical OncologyPediatric TumorsRadiation TherapyAdjuvant Radiotherapy After ResectionAtypical Teratoid Rhabdoid Tumor RadiotherapyMedian AgePediatric Brain Tumor RadiotherapyPrognostic Factors AnalysisSurvival Benefit AssessmentSurvival RatesTumor Location Assessment
AIM: To share a single center experience with 27 atypical teratoid/rhabdoid tumor (AT/RT) cases, and to determine the effect of gross total tumor resection and other clinical characteristics on the overall survival rate of AT/RT. MATERIAL AND METHODS: We included 27 patients-with a histopathologically confirmed primary intracranial childhood AT/ RT-who were operated in our clinic between January 2000 and December 2017. Age, sex, tumor location, disseminated disease, the presence of hydrocephalus, symptom duration till diagnosis, the extent of resection, and adjuvant radiotherapy were evaluated for their influence on overall survival. RESULTS: Median age at diagnosis for 27 patients was 19.1 months (7.2 months-5 years). Gross total resection was possible in 13 (48.72%) patients. Except for three patients who died of perioperative complications, all patients received chemotherapy and 11 received radiotherapy. In univariate analysis, male sex, older age at diagnosis (≥24 months), gross total resection, and radiotherapy were associated with overall longer survival; however, radiotherapy remained the only significant parameter in multivariate analysis. CONCLUSION: AT/RT is a rare and dreadful brain tumor that has low survival rates despite contemporary treatment. Radiotherapy seems to prolong survival; however, large-scale studies are needed to establish prognostic factors.
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Tanya Tekautz, Christine Fuller, Susan M. Blaney et al. · Journal of Clinical Oncology · 2005 · 426 citations · Full text
Medicine, Oncology, Pediatrics +17