TY - JOUR
T1 - Panel review of anaplastic oligodendroglioma from European Organization For Research and Treatment of Cancer Trial 26951
T2 - assessment of consensus in diagnosis, influence of 1p/19q loss, and correlations with outcome
AU - Kros, Johan M
AU - Gorlia, Thierry
AU - Kouwenhoven, Mathilde C
AU - Zheng, Ping-Pin
AU - Collins, V Peter
AU - Figarella-Branger, Dominique
AU - Giangaspero, Felice
AU - Giannini, Caterina
AU - Mokhtari, Karima
AU - Mørk, Sverre J
AU - Paetau, Anders
AU - Reifenberger, Guido
AU - van den Bent, Martin J
PY - 2007/6
Y1 - 2007/6
N2 - The diagnosis of anaplastic oligodendroglioma (AOD) or anaplastic oligoastrocytoma (AOA) is subject to interobserver variation. The aim of this study was to estimate consensus in typing and grading of these tumors using tumor material collected in a large prospective randomized phase III study and to correlate the consensus diagnosis with the 1p/19q status of the tumors and the clinical outcome. The available pathology material of the first 150 patients, randomized into the European Organization for Research and Treatment of Cancer Trial 26951, was reviewed by an independent panel of 9 neuropathologists. The presence of deletions of 1p and 19q was assessed by fluorescence in situ hybridization with locus-specific probes. The panel reached consensus on the diagnosis of AOD in 52% of the tumors that had been diagnosed as AOD by the local pathologists, whereas only 8% of the local diagnosis of AOA was confirmed with consensus. The concordance on the panel diagnosis of AOD was high (intraclass correlation = 86%). The survival curves for AOD with 1p/19q loss, AOD without these losses, and AOA without 1p/19q loss ran separately in this order. The absence of necrosis and the presence of endothelial abnormalities were correlated with better outcomes. In multivariate analysis, patients' age, 1p/19q loss, and necrosis were identified as independent prognostic factors.
AB - The diagnosis of anaplastic oligodendroglioma (AOD) or anaplastic oligoastrocytoma (AOA) is subject to interobserver variation. The aim of this study was to estimate consensus in typing and grading of these tumors using tumor material collected in a large prospective randomized phase III study and to correlate the consensus diagnosis with the 1p/19q status of the tumors and the clinical outcome. The available pathology material of the first 150 patients, randomized into the European Organization for Research and Treatment of Cancer Trial 26951, was reviewed by an independent panel of 9 neuropathologists. The presence of deletions of 1p and 19q was assessed by fluorescence in situ hybridization with locus-specific probes. The panel reached consensus on the diagnosis of AOD in 52% of the tumors that had been diagnosed as AOD by the local pathologists, whereas only 8% of the local diagnosis of AOA was confirmed with consensus. The concordance on the panel diagnosis of AOD was high (intraclass correlation = 86%). The survival curves for AOD with 1p/19q loss, AOD without these losses, and AOA without 1p/19q loss ran separately in this order. The absence of necrosis and the presence of endothelial abnormalities were correlated with better outcomes. In multivariate analysis, patients' age, 1p/19q loss, and necrosis were identified as independent prognostic factors.
KW - Brain Neoplasms/genetics
KW - Chromosomes, Human, Pair 1/genetics
KW - Chromosomes, Human, Pair 19/genetics
KW - Gene Deletion
KW - Humans
KW - In Situ Hybridization, Fluorescence
KW - Observer Variation
KW - Oligodendroglioma/genetics
KW - Prognosis
KW - Prospective Studies
KW - Survival Analysis
U2 - 10.1097/01.jnen.0000263869.84188.72
DO - 10.1097/01.jnen.0000263869.84188.72
M3 - Article
C2 - 17549014
SN - 0022-3069
VL - 66
SP - 545
EP - 551
JO - Journal of Neuropathology and Experimental Neurology
JF - Journal of Neuropathology and Experimental Neurology
IS - 6
ER -