Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2117282 | Cancer/Radiothérapie | 2015 | 11 Pages |
Abstract
Medulloblastoma are cerebellar tumours belonging to the group of primitive neuroectodermal tumours (PNET) and are the most common malignant brain tumours of childhood. These tumours are rare and heterogeneous, requiring some multicentric prospective studies and multidisciplinary care. The classical therapeutic approaches are based on clinical, radiological and surgical data. They involve surgery, radiation therapy and chemotherapy. Some histological features were added to characterize risk. More recently, molecular knowledge has allowed to devise risk-adapted strategies and helped to define groups with good outcome and reduce long-term sequelae, improve the prognostic of high-risk medulloblastoma and develop new therapeutic tools.
Related Topics
Life Sciences
Biochemistry, Genetics and Molecular Biology
Cancer Research
Authors
C. Vigneron, N. Entz-Werlé, P. Lutz, A. Spiegel, S. Jannier, S. Helfre, C. Alapetite, A. Coca, P. Kehrli, G. Noël,