» Articles » PMID: 21516462

Prognostic Stratification of Gliomatosis Cerebri by IDH1 R132H and INA Expression

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.

Citing Articles

A Novel 16-Genes Signature Scoring System as Prognostic Model to Evaluate Survival Risk in Patients with Glioblastoma.

Yu Z, Du M, Lu L Biomedicines. 2022; 10(2).

PMID: 35203526 PMC: 8869708. DOI: 10.3390/biomedicines10020317.


Gliomatosis cerebri mimicking diffuse demyelinating disease: Case Report.

Mingomataj E, Soleiman A, Sajan A, Velayudhan V Radiol Case Rep. 2020; 15(9):1683-1688.

PMID: 32742528 PMC: 7387734. DOI: 10.1016/j.radcr.2020.06.043.


Clinical relevance of molecular subgrouping of gliomatosis cerebri per 2016 WHO classification: a clinicopathological study of 89 cases.

Kwon M, Kang S, Cho H, Lee J, Kim S, Suh Y Brain Pathol. 2019; 30(2):235-245.

PMID: 31435963 PMC: 8018049. DOI: 10.1111/bpa.12782.


Wide Range of Clinical Outcomes in Patients with Gliomatosis Cerebri Growth Pattern: A Clinical, Radiographic, and Histopathologic Study.

Ly K, Oakley D, Pine A, Frosch M, Chiou S, Betensky R Oncologist. 2018; 24(3):402-413.

PMID: 30097523 PMC: 6519760. DOI: 10.1634/theoncologist.2018-0086.


Incidence and survival of gliomatosis cerebri: a population-based cancer registration study.

Georgakis M, Spinos D, Pourtsidis A, Psyrri A, Panourias I, Sgouros S J Neurooncol. 2018; 138(2):341-349.

PMID: 29464663 DOI: 10.1007/s11060-018-2802-z.


References
1.
Capper D, Weissert S, Balss J, Habel A, Meyer J, Jager D . Characterization of R132H mutation-specific IDH1 antibody binding in brain tumors. Brain Pathol. 2009; 20(1):245-54. PMC: 8094636. DOI: 10.1111/j.1750-3639.2009.00352.x. View

2.
Ducray F, Idbaih A, De Reynies A, Bieche I, Thillet J, Mokhtari K . Anaplastic oligodendrogliomas with 1p19q codeletion have a proneural gene expression profile. Mol Cancer. 2008; 7:41. PMC: 2415112. DOI: 10.1186/1476-4598-7-41. View

3.
Capper D, Zentgraf H, Balss J, Hartmann C, von Deimling A . Monoclonal antibody specific for IDH1 R132H mutation. Acta Neuropathol. 2009; 118(5):599-601. DOI: 10.1007/s00401-009-0595-z. View

4.
Ducray F, Criniere E, Idbaih A, Mokhtari K, Marie Y, Paris S . alpha-Internexin expression identifies 1p19q codeleted gliomas. Neurology. 2009; 72(2):156-61. DOI: 10.1212/01.wnl.0000339055.64476.cb. View

5.
Labussiere M, Idbaih A, Wang X, Marie Y, Boisselier B, Falet C . All the 1p19q codeleted gliomas are mutated on IDH1 or IDH2. Neurology. 2010; 74(23):1886-90. DOI: 10.1212/WNL.0b013e3181e1cf3a. View