Clinical impact of molecular biomarkers in gliomas

被引:59
作者
Siegal, Tali [1 ]
机构
[1] Rabin Med Ctr, Davidoff Inst Oncol, Ctr Neurooncol, IL-49100 Petah Tiqwa, Israel
关键词
Astrocytoma; Biomarkers; Glioma; Oligodendroglioma; Predictive; Prognostic; MGMT PROMOTER METHYLATION; NEWLY-DIAGNOSED GLIOBLASTOMA; INTEGRATED GENOMIC ANALYSIS; OLIGODENDROGLIAL TUMORS; IDH1; MUTATIONS; MALIGNANT ASTROCYTOMAS; DNA METHYLATION; FREQUENT ATRX; MUTANT IDH1; TEMOZOLOMIDE;
D O I
10.1016/j.jocn.2014.10.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 BRAE fusion or point mutation is highlighted. The potential of molecular biomarker-based classification to guide future therapeutic approach is discussed and accentuated. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:437 / 444
页数:8
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