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Prognostic Relevance of Histomolecular Classification of Diffuse Adult High-Grade Gliomas with Necrosis

机译:成人弥漫性高级别胶质瘤坏死的组织学分类与预后的相关性

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Diffuse adult high-grade gliomas (HGGs) with necrosis encompass anaplastic oligodendrogliomas (AOs) with necrosis (grade III), glioblastomas (GBM, grade IV) and glioblastomas with an oligodendroglial component (GBMO, grade IV). Here, we aimed to search for prognostic relevance of histological classification and molecular alterations of these tumors. About 210 patients were included (63 AO, 56 GBM and 91 GBMO). GBMO group was split into anaplastic oligoastrocytoma (AOA) with necrosis grade IV/GBMO, restricted to tumors showing intermingled astrocytic and oligodendroglial component, and GBM/GBMO based on tumors presenting oligodendroglial foci and features of GBM. Genomic arrays, IDH1 R132H expression analyses and IDH direct sequencing were performed. 1p/19q co-deletion characterized AO, whereas no IDH1 R132H expression and intact 1p/19q characterized both GBM and GBM/GBMO. AOA with necrosis/GBMO mainly demonstrated IDH1 R132H expression and intact 1p/19q. Other IDH1 or IDH2 mutations were extremely rare. Both histological and molecular classifications were predictive of progression free survival (PFS) and overall survival (OS) (P<10(-4)). Diffuse adult HGGs with necrosis can be split into three histomolecular groups of prognostic relevance: 1p/19q co-deleted AO, IDH1 R132H-GBM and 1p/19q intact IDH1 R132H+ gliomas that might be classified as IDH1 R132H+ GBM. Because of histomolecular heterogeneity, we suggest to remove the name GBMO.
机译:弥漫性成人坏死性高级别神经胶质瘤(HGG)包括变性坏死性少突胶质神经胶质瘤(AOs)(III级),胶质母细胞瘤(GBM,IV级)和具有少突胶质神经胶质成分的胶质母细胞瘤(GBMO,IV级)。在这里,我们旨在寻找这些肿瘤的组织学分类和分子改变的预后相关性。包括约210名患者(63 AO,56 GBM和91 GBMO)。 GBMO组被分为坏死级IV / GBMO的间变性少星形胶质细胞瘤(AOA),仅限于显示星形胶质细胞和少突神经胶质成分混合的肿瘤,以及基于表现出少突神经胶质病灶和GBM特征的肿瘤的GBM / GBMO。进行基因组阵列,IDH1 R132H表达分析和IDH直接测序。 1p / 19q共缺失表征AO,而没有IDH1 R132H表达和完整的1p / 19q表征GBM和GBM / GBMO。坏死/ GBMO的AOA主要表现出IDH1 R132H表达和完整的1p / 19q。其他IDH1或IDH2突变极为罕见。组织学和分子分类均预测无进展生存期(PFS)和总体生存期(OS)(P <10(-4))。具有坏死的弥漫性成人HGGs可分为三组具有预后相关性的组织分子:1p / 19q共缺失的AO,IDH1 R132H-GBM和1p / 19q完整的IDH1 R132H +胶质瘤,可能被分类为IDH1 R132H + GBM。由于组织分子的异质性,我们建议删除名称GBMO。

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