Prognostic stratification of gliomatosis cerebri by IDH1 R132H and INA expression

J Neurooncol. 2011 Nov;105(2):219-24. doi: 10.1007/s11060-011-0587-4. Epub 2011 Apr 24.

Abstract

Gliomatosis cerebri (GC) constitutes a heterogeneous group of conditions involving diffuse neoplastic glial cell infiltration of the brain. Management is difficult and an obvious challenge is to identify prognostic factors. Alpha-internexin (INA) expression, which is closely related to the 1p19q codeletion, is a strong prognostic marker in oligodendroglial tumors. Similarly, the R132H isocitrate dehydrogenase 1 IDH1 mutation, which can now be detected by use of a specific antibody, predicts better outcome in gliomas. In a retrospective series of 40 GC treated with up-front chemotherapy, we analyzed IDH1(R132H) mutant protein and INA immunohistochemical expression and correlated it with outcome; 17/40 GC expressed IDH1(R132H) and 10/40 GC expressed INA. IDH1(R132H) staining was strongly related to progression-free survival (42.3 vs. 15.5 months for positive IDH1(R132H) vs. negative tumors; P < 0.0001) and overall survival (73.9 vs. 23.6 months; P < 0.0001). This effect was independent of grade, histologic subtype, and INA expression (P < 0.001). Combined expression of IDH1(R132H) and INA was strongly associated with response to chemotherapy (100% vs. 36%; P = 0.003). These data strongly suggest that INA and IDH1(R132H) mutant protein immunohistochemical analysis is of a great prognostic value in biopsied GC.

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Follow-Up Studies
  • Humans
  • Immunoenzyme Techniques
  • Intermediate Filament Proteins / metabolism*
  • Isocitrate Dehydrogenase / metabolism*
  • Mutant Proteins / metabolism*
  • Neoplasms, Neuroepithelial / drug therapy
  • Neoplasms, Neuroepithelial / metabolism*
  • Neoplasms, Neuroepithelial / mortality
  • Polymorphism, Single Nucleotide / genetics*
  • Prognosis
  • Retrospective Studies
  • Survival Rate

Substances

  • Intermediate Filament Proteins
  • Mutant Proteins
  • alpha-internexin
  • Isocitrate Dehydrogenase
  • IDH1 protein, human