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胶质母细胞瘤患者超长生存期的全基因组分析。

Genome-Wide Analysis of Glioblastoma Patients with Unexpectedly Long Survival.

机构信息

Department of Pathology, State University of New York, Upstate Medical University, Syracuse, New York.

Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas.

出版信息

J Neuropathol Exp Neurol. 2019 Jun 1;78(6):501-507. doi: 10.1093/jnen/nlz025.

Abstract

Glioblastoma (GBM), representing WHO grade IV astrocytoma, is a relatively common primary brain tumor in adults with an exceptionally dismal prognosis. With an incidence rate of over 10 000 cases in the United States annually, the median survival rate ranges from 10-15 months in IDH1/2-wildtype tumors and 24-31 months in IDH1/2-mutant tumors, with further variation depending on factors such as age, MGMT methylation status, and treatment regimen. We present a cohort of 4 patients, aged 37-60 at initial diagnosis, with IDH1-mutant GBMs that were associated with unusually long survival intervals after the initial diagnosis, currently ranging from 90 to 154 months (all still alive). We applied genome-wide profiling with a methylation array (Illumina EPIC Array 850k) and a next-generation sequencing panel to screen for genetic and epigenetic alterations in these tumors. All 4 tumors demonstrated methylation patterns and genomic alterations consistent with GBM. Three out of four cases showed focal amplification of the CCND2 gene or gain of the region on 12p that included CCND2, suggesting that this may be a favorable prognostic factor in GBM. As this study has a limited sample size, further evaluation of patients with similar favorable outcome is warranted to validate these findings.

摘要

胶质母细胞瘤(GBM),代表 WHO 分级 IV 星形细胞瘤,是成人中相对常见的原发性脑肿瘤,预后极差。在美国,每年的发病率超过 10000 例,IDH1/2 野生型肿瘤的中位生存期在 10-15 个月之间,IDH1/2 突变型肿瘤的生存期在 24-31 个月之间,进一步的变化取决于年龄、MGMT 甲基化状态和治疗方案等因素。我们报告了 4 例患者的队列,在初始诊断时年龄为 37-60 岁,患有 IDH1 突变型 GBM,在初始诊断后具有异常长的生存间隔,目前从 90 到 154 个月不等(均存活)。我们应用全基因组甲基化谱分析(Illumina EPIC Array 850k)和下一代测序面板来筛选这些肿瘤中的遗传和表观遗传改变。所有 4 个肿瘤均表现出与 GBM 一致的甲基化模式和基因组改变。4 例中有 3 例显示 CCND2 基因的局灶性扩增或包含 CCND2 的 12p 区域的获得,表明这可能是 GBM 的一个有利预后因素。由于本研究的样本量有限,需要进一步评估具有类似有利结局的患者,以验证这些发现。

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