New perspectives in the treatment of adult medulloblastoma in the era of molecular oncology

Crit Rev Oncol Hematol. 2015 Jun;94(3):348-59. doi: 10.1016/j.critrevonc.2014.12.016. Epub 2014 Dec 31.

Abstract

Medulloblastoma is the most common central nervous system tumor in children, while it is extremely rare in adults. Multimodal treatment involving surgery, radiotherapy and chemotherapy can improve the prognosis of this disease, and recent advances in molecular biology have allowed the identification of molecular subgroups (WNT, SHH, Groups 3 and 4), each of which have different cytogenetic, mutational and gene expression signatures, demographics, histology and prognosis. The present review focuses on the state of the art for adult medulloblastoma treatment and on novel molecular advances and their future implications in the treatment of this disease.

Keywords: Adults; Medulloblastoma; SHH; Treatment; WNT.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adult
  • Age Factors
  • Cerebellar Neoplasms / diagnosis
  • Cerebellar Neoplasms / etiology
  • Cerebellar Neoplasms / therapy*
  • Combined Modality Therapy
  • Diagnostic Imaging
  • Epigenesis, Genetic
  • Genetic Variation
  • Humans
  • Medulloblastoma / diagnosis
  • Medulloblastoma / etiology
  • Medulloblastoma / therapy*
  • Neoplasm Recurrence, Local
  • Neoplasm Staging
  • Signal Transduction
  • Treatment Outcome