Molecular Pathogenesis and Emerging Treatment for Glioblastoma

被引:10
|
作者
Ramos, Alexander D. [1 ]
Magge, Rajiv S. [2 ]
Ramakrishna, Rohan [1 ]
机构
[1] Weill Cornell Med Coll, Dept Neurol Surg, New York, NY 10065 USA
[2] Weill Cornell Med Coll, Dept Neurol, New York, NY USA
关键词
Brain tumor; Glioblastoma; Molecular; Receptor tyrosine kinases; Stem cells; LONG-NONCODING RNA; GROWTH-FACTOR RECEPTOR; NEWLY-DIAGNOSED GLIOBLASTOMA; PHASE-II TRIAL; INTEGRATED GENOMIC ANALYSIS; SINGLE-AGENT BEVACIZUMAB; TERT PROMOTER MUTATIONS; INTRATUMORAL HETEROGENEITY; ADJUVANT TEMOZOLOMIDE; EXPRESSION PROFILES;
D O I
10.1016/j.wneu.2018.04.021
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Glioblastoma is the most common primary malignant brain tumor, with more than10,000 new cases each year in the United States. Significant basic science and clinical research has been devoted to understanding this disease, yet median survival with standard of care treatment remains approximately 15 months. Over the past decade, advances in genomic sequencing technology, biostatistics, and computing have allowed for an unprecedented ability to profile the gene expression patterns and mutations driving the formation of tumors. These advances have generated both prognostic information as well as a multitude of treatment targets that are just now coming into clinical practice. This article aims to provide a comprehensive update on the recent use of genetic profiling to identify the molecular pathways altered in glioblastoma and to describe ongoing clinical trials to exploit these pathways for treatment.
引用
收藏
页码:495 / 504
页数:10
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