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Medulloblastoma: From Molecular Pathology to Therapy
Medulloblastoma is the most common malignant tumor of central nervous system in children. Patients affected by medulloblastoma may be categorized as high-risk and standard-risk patients, based on the clinical criteria and histologic features of the disease. Currently, multimodality treatment, includ...
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Published in: | Clinical cancer research 2008-02, Vol.14 (4), p.971-976 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Medulloblastoma is the most common malignant tumor of central nervous system in children. Patients affected by medulloblastoma
may be categorized as high-risk and standard-risk patients, based on the clinical criteria and histologic features of the
disease. Currently, multimodality treatment, including surgery, radiotherapy, and chemotherapy is considered as the most effective
strategy against these malignant cerebellar tumors of the childhood. Despite the potential poor outcomes of these lesions,
the 5-year survival stands, at present, at 70% to 80% for standard-risk patients, whereas high-risk patients have a 5-year
survival of 55% to 76%. Attempts to further reduce the morbidity and mortality associated with medulloblastoma have been restricted
by the toxicity of conventional treatments and the infiltrative nature of the disease. Over the past decade, new discoveries
in molecular biology have revealed new insights in signaling pathways regulating medulloblastoma tumor formation. Recent advances
in the molecular biology of medulloblastoma indicate that the classification of these embryonal tumors, solely based on histology
and clinical criteria, may not be adequate enough. Better understanding of the growth control mechanisms involved in the development
and progression of medulloblastoma will allow a better classification, leading to the improvement of the existing therapies,
as well as to the development of new therapeutic approaches. |
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ISSN: | 1078-0432 1557-3265 |
DOI: | 10.1158/1078-0432.CCR-07-2072 |