Diagnostic and Therapeutic Biomarkers in Glioblastoma: Current Status and Future Perspectives

被引:217
|
作者
Szopa, Wojciech [1 ]
Burley, Thomas A. [2 ]
Kramer-Marek, Gabriela [2 ]
Kaspera, Wojciech [1 ]
机构
[1] Med Univ Silesia, Reg Hosp, Dept Neurosurg, Sosnowiec, Poland
[2] Inst Canc Res, Div Radiotherapy & Imaging, London, England
关键词
GROWTH-FACTOR RECEPTOR; MGMT PROMOTER METHYLATION; INTEGRATED GENOMIC ANALYSIS; MULTICENTER PHASE-II; HIGH-GRADE GLIOMAS; DNA-REPAIR GENE; PROGNOSTIC-SIGNIFICANCE; MALIGNANT ASTROCYTOMAS; ADJUVANT TEMOZOLOMIDE; MOLECULAR BIOMARKERS;
D O I
10.1155/2017/8013575
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Glioblastoma (GBM) is a primary neuroepithelial tumor of the central nervous system, characterized by an extremely aggressive clinical phenotype. Patients with GBM have a poor prognosis and only 3-5% of them survive for more than 5 years. The current GBM treatment standards include maximal resection followed by radiotherapy with concomitant and adjuvant therapies. Despite these aggressive therapeutic regimens, the majority of patients suffer recurrence due to molecular heterogeneity of GBM. Consequently, a number of potential diagnostic, prognostic, and predictive biomarkers have been investigated. Some of them, such as IDH mutations, 1p19q deletion, MGMT promoter methylation, and EGFRvIII amplification are frequently tested in routine clinical practice. With the development of sequencing technology, detailed characterization of GBM molecular signatures has facilitated a 6more personalized therapeutic approach and contributed to the development of a new generation of anti-GBM therapies such as molecular inhibitors targeting growth factor receptors, vaccines, antibody-based drug conjugates, and more recently inhibitors blocking the immune checkpoints. In this article, we review the exciting progress towards elucidating the potential of current and novel GBM biomarkers and discuss their implications for clinical practice.
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页数:13
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