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分子生物标志物在胶质瘤中的临床影响。

Clinical impact of molecular biomarkers in gliomas.

作者信息

Siegal Tali

机构信息

Center for Neuro-Oncology, Davidoff Institute of Oncology, Rabin Medical Center, Campus Beilinson, 49100 Petach Tikva, Israel.

出版信息

J Clin Neurosci. 2015 Mar;22(3):437-44. doi: 10.1016/j.jocn.2014.10.004. Epub 2014 Dec 18.

Abstract

The World Health Organization (WHO) classification system for glial tumors provides guidance as to the predicted course of the disease and choice of treatment. However, histologically identical tumors may have a very different outcome and response to treatment. Molecular markers that carry both diagnostic and prognostic information add valuable tools by redefining tumor subtypes within each WHO category. Therefore, molecular biomarkers have become an integral part of tumor assessment in modern neuro-oncology and biomarker status now guides clinical decisions in some subtypes of gliomas, including anaplastic oligodendroglioma and glioblastoma in the elderly. This review discusses the prognostic and predictive impact of molecular markers that have undergone extensive study in recent years. The clinical relevance of contemporary molecular classification of gliomas using the routine assessment of IDH mutations, promoter methylation of MGMT, chromosomal deletion of 1p/19q, mutations of EGFR and ATRX genes, and BRAF fusion or point mutation is highlighted. The potential of molecular biomarker-based classification to guide future therapeutic approach is discussed and accentuated.

摘要

世界卫生组织(WHO)的神经胶质瘤分类系统为疾病的预测病程和治疗选择提供了指导。然而,组织学上相同的肿瘤可能具有非常不同的预后和对治疗的反应。携带诊断和预后信息的分子标志物通过重新定义每个WHO类别中的肿瘤亚型,增加了有价值的工具。因此,分子生物标志物已成为现代神经肿瘤学中肿瘤评估不可或缺的一部分,生物标志物状态现在指导着某些类型胶质瘤的临床决策,包括间变性少突胶质细胞瘤和老年胶质母细胞瘤。本综述讨论了近年来经过广泛研究的分子标志物的预后和预测影响。强调了使用IDH突变的常规评估、MGMT启动子甲基化、1p/19q染色体缺失、EGFR和ATRX基因突变以及BRAF融合或点突变对胶质瘤进行当代分子分类的临床相关性。讨论并强调了基于分子生物标志物的分类指导未来治疗方法的潜力。

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