Malignant clinical features of anaplastic gliomas without IDH mutation

Neuro Oncol. 2015 Jan;17(1):136-44. doi: 10.1093/neuonc/nou112. Epub 2014 Jun 23.

Abstract

Background: Diagnosis of WHO grade III anaplastic gliomas does not always correspond to its clinical outcome because of the isocitrate dehydrogenase (IDH) gene status. Anaplastic gliomas without IDH mutation result in a poor prognosis, similar to grade IV glioblastomas. However, the malignant features of anaplastic gliomas without IDH mutation are not well understood. The aim of this study was to examine anaplastic gliomas, in particular those without IDH mutation, with regard to their malignant features, recurrence patterns, and association with glioma stem cells.

Methods: We retrospectively analyzed 86 cases of WHO grade III anaplastic gliomas. Data regarding patient characteristics, recurrence pattern, and prognosis were obtained from medical records. We examined molecular alterations such as IDH mutation, 1p19q loss, TP53 mutation, MGMT promoter methylation, Ki67 labeling index, and CD133, SOX2, and NESTIN expression.

Results: Of the 86 patients with anaplastic gliomas, 58 carried IDH mutation, and 40 experienced recurrence. The first recurrence was local in 25 patients and distant in 15. Patients without IDH mutation exhibited significantly higher CD133 and SOX2 expression (P = .025 and .020, respectively) and more frequent distant recurrence than those with IDH mutation (P = .022).

Conclusions: Patients with anaplastic gliomas without IDH mutation experienced distant recurrence and exhibited glioma stem cell markers, indicating that this subset may share some malignant characteristics with glioblastomas.

Keywords: CD133; IDH; anaplastic gliomas; distant recurrence; grade III gliomas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AC133 Antigen
  • Adult
  • Antigens, CD / metabolism
  • Brain Neoplasms / genetics*
  • Brain Neoplasms / metabolism
  • Female
  • Glioma / genetics*
  • Glioma / metabolism
  • Glycoproteins / metabolism
  • Humans
  • Isocitrate Dehydrogenase / genetics*
  • Male
  • Middle Aged
  • Mutation*
  • Neoplasm Grading
  • Peptides / metabolism
  • SOXB1 Transcription Factors / metabolism

Substances

  • AC133 Antigen
  • Antigens, CD
  • Glycoproteins
  • PROM1 protein, human
  • Peptides
  • SOX2 protein, human
  • SOXB1 Transcription Factors
  • Isocitrate Dehydrogenase
  • IDH1 protein, human