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Medulloblastomas

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Textbook of Pediatric Neurosurgery

Abstract

Medulloblastomas are embryonal cerebellar tumors and the most common central nervous system malignancies in children. While progress in clinical management dramatically improved outcomes for what was once a uniformly fatal disease, the prognosis for children with metastatic or recurrent medulloblastoma remains poor despite intensive multimodal therapy. As we reach a limit of effect and toxicities with conventional therapies, a new understanding of medulloblastoma biology has emerged, paving the way for the next generation of clinical trials. Current consensus identifies four medulloblastoma entities – WNT, SHH, Group 3, and Group 4 – with distinct clinical presentations, genetic and molecular features, responses to therapy, and patterns of relapse. The first prospective studies designed to deliver subgroup-specific treatment are underway and hold the promise of better survival outcomes and fewer long-term toxicities.

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Stucklin, A.S.G., Kuzan-Fischer, C.M., Taylor, M.D. (2018). Medulloblastomas. In: Di Rocco, C., Pang, D., Rutka, J. (eds) Textbook of Pediatric Neurosurgery. Springer, Cham. https://doi.org/10.1007/978-3-319-31512-6_91-1

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