Molecular Heterogeneity in Glioblastoma: Therapeutic Opportunities and Challenges

被引:53
作者
Nicholas, M. Kelly [1 ]
Lukas, Rimas V.
Chmura, Steven [2 ]
Yamini, Bakhtihar [3 ]
Lesniak, Maciej [3 ]
Pytel, Peter [4 ]
机构
[1] Univ Chicago, Med Ctr, Dept Neurol, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Radiat & Cellular Oncol, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Surg, Neurosurg Sect, Chicago, IL 60637 USA
[4] Univ Chicago, Dept Pathol, Sect Neuropathol, Chicago, IL 60637 USA
关键词
PHASE-II TRIAL; NEURAL STEM-CELLS; ADJUVANT TEMOZOLOMIDE; TEMSIROLIMUS CCI-779; RECURRENT; BRAIN; MULTIFORME; GROWTH; GLIOMA; CONCOMITANT;
D O I
10.1053/j.seminoncol.2011.01.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glioblastoma (GBM) has been recognized as a clinical and pathologic entity for more than a century. Throughout its history, its cells of origin have been in question. Its behavior is aggressive and despite decades of effort, median survival is just beginning to improve. Surgical techniques and radiotherapy schemas continue to be refined, but the most recent progress has been achieved through improved medical therapies. These are the result of both pharmacological advances and a deeper understanding of the biological characteristics of GBM. Due to a combination of its complex phenotype and organ-specific clinical manifestations, efforts to refine GBM treatment with targeted therapies largely have been frustrated. In this review, we discuss recent attempts to exploit new molecular insights, consider the reasons for slow progress in developing better treatments, and examine future therapeutic options. © 2011 Elsevier Inc.
引用
收藏
页码:243 / 253
页数:11
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