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NCCN 指南解读:中枢神经系统肿瘤,第 1.2017 版。

NCCN Guidelines Insights: Central Nervous System Cancers, Version 1.2017.

出版信息

J Natl Compr Canc Netw. 2017 Nov;15(11):1331-1345. doi: 10.6004/jnccn.2017.0166.

Abstract

For many years, the diagnosis and classification of gliomas have been based on histology. Although studies including large populations of patients demonstrated the prognostic value of histologic phenotype, variability in outcomes within histologic groups limited the utility of this system. Nonetheless, histology was the only proven and widely accessible tool available at the time, thus it was used for clinical trial entry criteria, and therefore determined the recommended treatment options. Research to identify molecular changes that underlie glioma progression has led to the discovery of molecular features that have greater diagnostic and prognostic value than histology. Analyses of these molecular markers across populations from randomized clinical trials have shown that some of these markers are also predictive of response to specific types of treatment, which has prompted significant changes to the recommended treatment options for grade III (anaplastic) gliomas.

摘要

多年来,神经胶质瘤的诊断和分类一直基于组织学。尽管包括大量患者的研究表明了组织表型的预后价值,但组织学分组内的结果变异性限制了该系统的实用性。尽管如此,组织学是当时唯一经过验证且广泛可用的工具,因此它被用于临床试验的纳入标准,从而决定了推荐的治疗选择。为了确定导致神经胶质瘤进展的分子变化而进行的研究导致发现了比组织学更具诊断和预后价值的分子特征。对来自随机临床试验的人群进行这些分子标志物的分析表明,其中一些标志物也可以预测对特定类型治疗的反应,这促使对 III 级(间变性)神经胶质瘤的推荐治疗选择进行了重大更改。

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