Antiangiogenic Therapy for Glioblastoma: Current Status and Future Prospects

被引:116
作者
Batchelor, Tracy T. [1 ,2 ]
Reardon, David A. [2 ,3 ]
de Groot, John F. [4 ]
Wick, Wolfgang [5 ,6 ]
Weller, Michael [7 ,8 ]
机构
[1] Massachusetts Gen Hosp, Stephen E & Catherine Pappas Ctr Neurooncol, Ctr Canc, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Dana Farber Canc Inst, Ctr Neurooncol, Boston, MA 02115 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Neurooncol, Houston, TX 77030 USA
[5] Univ Clin Heidelberg, Heidelberg, Germany
[6] German Canc Res Ctr, German Canc Consortium DKTK, Heidelberg, Germany
[7] Univ Zurich Hosp, Dept Neurol, CH-8091 Zurich, Switzerland
[8] Univ Zurich Hosp, Brain Tumor Ctr, CH-8091 Zurich, Switzerland
关键词
NEWLY-DIAGNOSED GLIOBLASTOMA; RECURRENT MALIGNANT GLIOMAS; ANTI-VEGF THERAPY; POSITRON-EMISSION-TOMOGRAPHY; STANDARD RADIATION-THERAPY; TYROSINE KINASE INHIBITOR; SINGLE-AGENT BEVACIZUMAB; PHASE I/II TRIAL; DAILY TEMOZOLOMIDE; TUMOR VASCULATURE;
D O I
10.1158/1078-0432.CCR-14-0834
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glioblastoma is characterized by high expression levels of proangiogenic cytokines and microvascular proliferation, highlighting the potential value of treatments targeting angiogenesis. Antiangiogenic treatment likely achieves a beneficial impact through multiple mechanisms of action. Ultimately, however, alternative proangiogenic signal transduction pathways are activated, leading to the development of resistance, even in tumors that initially respond. The identification of biomarkers or imaging parameters to predict response and to herald resistance is of high priority. Despite promising phase II clinical trial results and patient benefit in terms of clinical improvement and longer progression-free survival, an overall survival benefit has not been demonstrated in four randomized phase III trials of bevacizumab or cilengitide in newly diagnosed glioblastoma or cediranib or enzastaurin in recurrent glioblastoma. However, future studies are warranted. Predictive markers may allow appropriate patient enrichment, combination with chemotherapy may ultimately prove successful in improving overall survival, and novel agents targeting multiple proangiogenic pathways may prove effective. (C)2014 AACR.
引用
收藏
页码:5612 / 5619
页数:8
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