基于分子肿瘤谱的胶质瘤个体化化疗展望。

Q2 Medicine Progress in neurological surgery Pub Date : 2018-01-01 Epub Date: 2018-01-25 DOI:10.1159/000467378
Riccardo Soffietti, Federica Franchino, Michela Magistrello, Alessia Pellerino, Roberta Rudà
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引用次数: 1

摘要

组织病理学分型和分级是世界卫生组织中枢神经系统肿瘤分类的基础。它为临床医生提供有关疾病自然过程的信息,从而指导治疗选择。然而,组织学相同的肿瘤患者可能有不同的结果和对治疗的反应。近年来,人们对MGMT启动子甲基化、1p/19q共缺失和IDH1/IDH2突变这三个在成人胶质瘤中的分子标记进行了广泛的研究。这些标记物可能具有预后价值,也可能具有预测价值,但由于两者可能同时存在,因此往往难以区分。目前,MGMT启动子甲基化被认为是胶质母细胞瘤对替莫唑胺化疗反应的预测标志物,特别是在老年患者中,1p/19q共缺失是少突胶质肿瘤的分子特征,也是间变性胶质瘤对PCV化疗反应的预测标志物,IDH1/IDH2突变在所有胶质瘤组织病理级别中都具有很强的有利预后价值。
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Perspectives of Personalized Chemotherapy of Gliomas Based on Molecular Tumor Profiling.

Histopathological typing and grading are the cornerstones of the World Health Organization classification of the central nervous system tumors. It provides clinicians with information on the natural course of the disease and thus guides therapeutic choices. Nonetheless, patients with histologically identical tumors may have different outcomes and response to therapy. In recent years, extensive research has been done on three molecular markers in adult gliomas, namely MGMT promoter methylation, 1p/19q co-deletion, and IDH1/IDH2 mutations. These markers may have either a prognostic or a predictive value, differentiation of which is often difficult as both can coexist. At present, MGMT promoter methylation is considered as a predictive marker for response of glioblastoma to chemotherapy with temozolomide, particularly in elderly patients, 1p/19q co-deletion is a molecular signature of oligodendroglial tumors and predictive marker for response of anaplastic gliomas to PCV chemotherapy, and IDH1/IDH2 mutations have a strong favorable prognostic value across all glioma histopathological grades.

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期刊介绍: Published since 1966, this series has become universally recognized as the most significant group of books serving neurological surgeons. Volumes feature contributions from distinguished international surgeons, who brilliantly review the literature from the perspective of their own personal experience. The result is a series of works providing critical distillations of developments of central importance to the theory and practice of neurological surgery.
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