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弥漫性胶质瘤中TERT启动子突变状态在常规临床环境中的诊断意义

Diagnostic implications of TERT promoter mutation status in diffuse gliomas in a routine clinical setting.

作者信息

Hewer Ekkehard, Prebil Nadine, Berezowska Sabina, Gutt-Will Marielena, Schucht Philippe, Dettmer Matthias S, Vassella Erik

机构信息

Institute of Pathology, University of Bern, Murtenstrasse 31, 3010, Bern, Switzerland.

Department of Neurosurgery, Inselspital, Bern University Hospital, University of Bern, 3010, Bern, Switzerland.

出版信息

Virchows Arch. 2017 Nov;471(5):641-649. doi: 10.1007/s00428-017-2216-x. Epub 2017 Aug 19.

Abstract

IDH (isocitrate dehydrogenase) gene mutations are present in most diffuse low-grade gliomas and define the clinico-pathological core of the respective morphologically defined entities. Conversely, according to the 2016 WHO classification, the majority of glioblastomas belong to the IDH-wildtype category, which is defined by exclusion. TERT (telomerase reverse transcriptase gene) promoter mutations have been suggested as a molecular marker for primary glioblastomas. We analyzed molecular, histopathological, and clinical profiles of a series of 110 consecutive diffuse gliomas (WHO grades II-IV) diagnosed at our institution, in which TERT promoter mutation analysis had been performed as part of diagnostic work-up. A diagnostic algorithm based on IDH, TERT, ATRX, H3F3A, and 1p19q co-deletion status resulted in a consistent molecular classification with only 14 (13%) marker-negative tumors. TERT promoter mutations were present in 77% of IDH-wildtype tumors. The TERT/IDH-wildtype category was highly enriched for tumors with unconventional clinical or histological features. Molecular classes were associated with distinct rates of MGMT promoter methylation. We conclude that, in a routine diagnostic setting, TERT promoter mutations define a relatively homogeneous core group among IDH-wildtype diffuse gliomas that includes the majority of primary glioblastomas as well as their putative precursor lesions.

摘要

异柠檬酸脱氢酶(IDH)基因突变存在于大多数弥漫性低级别胶质瘤中,并界定了各自形态学定义实体的临床病理核心。相反,根据2016年世界卫生组织(WHO)分类,大多数胶质母细胞瘤属于IDH野生型类别,该类别通过排除法定义。端粒酶逆转录酶基因(TERT)启动子突变已被认为是原发性胶质母细胞瘤的分子标志物。我们分析了在我们机构诊断的一系列110例连续弥漫性胶质瘤(WHO二级至四级)的分子、组织病理学和临床特征,其中TERT启动子突变分析已作为诊断检查的一部分进行。基于IDH、TERT、ATRX、H3F3A和1p19q共缺失状态的诊断算法产生了一致的分子分类,仅有14例(13%)标志物阴性肿瘤。TERT启动子突变存在于77%的IDH野生型肿瘤中。TERT/IDH野生型类别高度富集具有非常规临床或组织学特征的肿瘤。分子类别与不同的O6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)启动子甲基化率相关。我们得出结论,在常规诊断环境中,TERT启动子突变在IDH野生型弥漫性胶质瘤中定义了一个相对同质的核心组,其中包括大多数原发性胶质母细胞瘤及其假定的前驱病变。

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