Prognostic impact of the 2016 WHO classification of diffuse gliomas in the French POLA cohort

• DOI: 10.1007/s00401-016-1611-8
• Publication Date: 2016-08-29T02:18:27Z
• Authors: Emeline Tabouret; Anh Tuan Nguyen; Caroline Dehais; Catherine Carpentier; François Ducray; Ahmed Idbaih; Karima Mokhtari; Anne Jouvet; Emmanuelle Uro-Coste; Carole Colin; Olivier Chinot; Hugues Loiseau; Elisabeth Moyal; Claude-Alain Maurage; Marc Polivka; Emmanuèle Lechapt...; Christine Desenclos; David Meyronet; Jean-Yves Delattre; Dominique Figarel...
• Keywords: Anaplastic astrocytoma; Grading (engineering); Oligodendroglial Tumor; Univariate analysis; Progression-free survival

The new WHO classification of diffuse gliomas has been refined and now includes the 1p/19q codeletion, IDH1/2 mutation, and histone H3-K27M mutation. Our objective was to assess the prognostic value of the updated 2016 WHO classification in the French POLA cohort. All cases of high-grade oligodendroglial tumors sent for central pathological review and included into the French nationwide POLA cohort were reclassified according to the updated 4th WHO classification. In total, 1041 patients were included, with a median age at diagnosis of 50.4 years (range 17.1-84.4). Based on the new histomolecular classification, diagnoses included anaplastic oligodendroglioma IDH mutant and 1p/19q-codeleted (32.5 %), anaplastic astrocytoma IDH mutant (IDH (mut)) (11.0 %), anaplastic astrocytoma IDH wild type (IDH (wt)) (5.3 %), glioblastoma IDH (mut) (17.1 %), and glioblastoma IDH (wt) (33.2 %). Ten patients presented with a diffuse midline tumor, H3 K27M mutant. The new WHO classification was prognostic for progression-free survival (PFS) and overall survival (OS) (p < 0.001). We did not find prognosis differences between grades III and IV for IDH (mut) 1p/19q intact and IDH (wt) gliomas in univariate and multivariate analyses. Among anaplastic astrocytoma IDH (wt), cases with chromosome arm 7p gain and 10q loss (55 %) had shorter PFS than the others (p = 0.027). In conclusion, the new WHO histomolecular classification of diffuse gliomas presented with high prognostic value. Grading was not discriminant between grade III and IV high-grade gliomas.