Molecular targeting of glioblastoma: Drug discovery and therapies

被引:106
作者
Bai, Ren-Yuan [1 ]
Staedtke, Verena [1 ]
Riggins, Gregory J. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurosurg, Baltimore, MD 21231 USA
关键词
PHASE-II TRIAL; RECURRENT MALIGNANT GLIOMAS; TYROSINE KINASE INHIBITOR; SINGLE-AGENT BEVACIZUMAB; HIGH-GRADE GLIOMAS; RADIATION-THERAPY; BRAIN-TUMORS; DETAILED CHARACTERIZATION; IMATINIB MESYLATE; PLUS HYDROXYUREA;
D O I
10.1016/j.molmed.2011.01.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Despite advances in treatment for glioblastoma multiforme (GBM), patient prognosis remains poor. Although there is growing evidence that molecular targeting could translate into better survival for GBM, current clinical data show limited impact on survival. Recent progress in GBM genomics implicate several activated pathways and numerous mutated genes. This molecular diversity can partially explain therapeutic resistance and several approaches have been postulated to target molecular changes. Furthermore, most drugs are unable to reach effective concentrations within the tumor owing to elevated intratumoral pressure, restrictive vasculature and other limiting factors. Here, we describe the preclinical and clinical developments in treatment strategies of GBM. We review the current clinical trials for GBM and discuss the challenges and future directions of targeted therapies.
引用
收藏
页码:301 / 312
页数:12
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