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欧洲癌症研究与治疗组织26951试验中间变性少突胶质细胞瘤的专家组审查:诊断共识评估、1p/19q缺失的影响及与预后的相关性

Panel review of anaplastic oligodendroglioma from European Organization For Research and Treatment of Cancer Trial 26951: assessment of consensus in diagnosis, influence of 1p/19q loss, and correlations with outcome.

作者信息

Kros Johan M, Gorlia Thierry, Kouwenhoven Mathilde C, Zheng Ping-Pin, Collins V Peter, Figarella-Branger Dominique, Giangaspero Felice, Giannini Caterina, Mokhtari Karima, Mørk Sverre J, Paetau Anders, Reifenberger Guido, van den Bent Martin J

机构信息

Department of Pathology, Erasmus Medical Center, Rotterdam, The Netherlands.

出版信息

J Neuropathol Exp Neurol. 2007 Jun;66(6):545-51. doi: 10.1097/01.jnen.0000263869.84188.72.

Abstract

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.

摘要

间变性少突胶质细胞瘤(AOD)或间变性少突星形细胞瘤(AOA)的诊断存在观察者间差异。本研究的目的是利用一项大型前瞻性随机III期研究中收集的肿瘤材料,评估这些肿瘤在分型和分级方面的一致性,并将一致性诊断与肿瘤的1p/19q状态及临床结局相关联。对随机纳入欧洲癌症研究与治疗组织试验26951的前150例患者的可用病理材料,由9名神经病理学家组成的独立小组进行了复查。通过使用位点特异性探针的荧光原位杂交评估1p和19q缺失的存在情况。该小组对当地病理学家诊断为AOD的肿瘤中的52%达成了AOD诊断的共识,而AOA的当地诊断仅有8%得到了共识确认。小组对AOD诊断的一致性很高(组内相关系数=86%)。伴有1p/19q缺失的AOD、不伴有这些缺失的AOD以及不伴有1p/19q缺失的AOA的生存曲线依此呈分离状态。无坏死和存在内皮异常与较好的结局相关。在多因素分析中,患者年龄、1p/19q缺失和坏死被确定为独立的预后因素。

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