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首页> 外文期刊>Translational Oncology >Prognosis of Glioblastoma With Oligodendroglioma Component is Associated With the IDH1 Mutation and MGMT Methylation Status
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Prognosis of Glioblastoma With Oligodendroglioma Component is Associated With the IDH1 Mutation and MGMT Methylation Status

机译:胶质母细胞瘤合并少突胶质细胞瘤的预后与 IDH1 突变和 MGMT 甲基化状态有关

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Glioblastoma (GBM) with oligodendroglioma component (GBMO) is a newly described GBM subtype in the 2007 World Health Organization classification. However, its biological and genetic characteristics are largely unknown. We investigated the clinicopathological and molecular features of 34 GBMOs and compared the survival rate of these patients with those of patients with astrocytoma, oligodendroglioma, anaplastic oligoastrocytoma (AOA), and conventional GBMs in our hospital. GBMO could be divided into two groups based on the presence of an IDH1 mutation. The IDH1 mutation was more frequently found in secondary GBMO, which had lower frequencies of EGFR amplification but higher MGMT methylation than the wild type IDH1 group, and patients with mutant IDH1 GBMO were on average younger than those with wild-type IDH1 . Therefore, GBMO is a clinically and molecularly heterogeneous subtype, largely belonging to a proneural and classical subtype of GBM. The survival rate of GBMO patients itself was worse than that of AOA patients but not significantly better than that of conventional GBM patients. GBMO survival was independent of the dominant histopathological subtype i.e., astrocyte-dominant or oligodendroglioma -dominant, but it was significantly associated with the IDH1 mutation and MGMT methylation status. Therefore, GBMO should be regarded as a separate entity from AOA and must be classified as a subtype of GBM. However, further study is needed to determine whether it is a pathologic variant or a pattern of GBM because GBMO has a similar prognosis to conventional GBMs.
机译:胶质母细胞瘤(GBM)和少突胶质细胞瘤成分(GBMO)是2007年世界卫生组织分类中新描述的GBM亚型。但是,其生物学和遗传特性在很大程度上是未知的。我们调查了34种GBMO的临床病理和分子特征,并比较了这些患者与星形细胞瘤,少突胶质细胞瘤,间变性少星形细胞瘤(AOA)和常规GBM患者的生存率。根据IDH1突变的存在,GBMO可以分为两组。 IDH1突变在继发性GBMO中更常见,其EGFR扩增频率较低,但MGMT甲基化程度高于野生型IDH1组,且IDH1 GBMO突变的患者平均比野生型IDH1年轻。因此,GBMO是临床和分子上异质的亚型,主要属于GBM的pronerural和经典亚型。 GBMO患者本身的生存率比AOA患者差,但并不比传统GBM患者明显好。 GBMO的生存与主要的组织病理学亚型即星形胶质细胞或少突胶质细胞瘤无关,但与IDH1突变和MGMT甲基化状态显着相关。因此,GBMO应该被视为与AOA分开的实体,并且必须被归类为GBM的子类型。但是,由于GBMO的预后与常规GBM相似,因此需要进一步研究以确定其是GBM的病理变异还是模式。

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