Pathological and molecular heterogeneity of medulloblastoma

Curr Opin Oncol. 2008 Nov;20(6):668-75. doi: 10.1097/CCO.0b013e32831369f4.


Purpose of review: The outcome of medulloblastoma patients and the quality of life of survivors can be improved by both novel therapies and a better tumor classification. This review will focus on the pathology and molecular biology of medulloblastoma and its potential to influence risk assignment and future therapy.

Recent findings: A risk stratification system of pediatric medulloblastoma based on a combination of histopathological evaluation and targeted molecular analysis can be outlined. Among the four variants recognized by the 2007 WHO classification, the desmoplastic medulloblastoma and the medulloblastoma with extensive nodularity have significantly better survival with respect to classic medulloblastoma, whereas the large-cell and anaplastic have a worse prognosis. Moreover, 17p loss, MYC amplification/expression, and 1q gain are associated with poor prognosis; in contrast, monosomy 6, mutation of CTNNB1, and trkC expression identify tumors with a favorable outcome. Emerging evidence indicates that the different precursor cell populations that form the cerebellum are susceptible to mutations in signal pathways that regulate their functions; these mutations alter normal development programmes and may result in the formation of distinct variants of medulloblastoma.

Summary: Better understanding of the growth control mechanisms involved in the development and progression of medulloblastoma will allow improved therapeutic stratification of patients using existing adjuvant therapy as well as the development of new therapeutic approaches.

Publication types

  • Review

MeSH terms

  • Adolescent
  • Brain Neoplasms / drug therapy*
  • Cerebellum / pathology
  • Child
  • Child, Preschool
  • Gene Expression Regulation, Neoplastic*
  • Hedgehog Proteins / metabolism
  • Humans
  • Infant
  • Infant, Newborn
  • Medulloblastoma / drug therapy*
  • Quality of Life
  • Receptors, Notch / metabolism
  • Risk
  • Treatment Outcome
  • Wnt Proteins / metabolism


  • Hedgehog Proteins
  • Receptors, Notch
  • Wnt Proteins