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Antiangiogenic therapy for glioblastoma: current status and future prospects.
- Source :
-
Clinical cancer research : an official journal of the American Association for Cancer Research [Clin Cancer Res] 2014 Nov 15; Vol. 20 (22), pp. 5612-9. - Publication Year :
- 2014
-
Abstract
- 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.<br /> (©2014 American Association for Cancer Research.)
- Subjects :
- Biomarkers metabolism
Brain Neoplasms pathology
Clinical Trials as Topic
Diagnostic Imaging
Drug Resistance, Neoplasm
Glioblastoma diagnosis
Glioblastoma metabolism
Glioblastoma pathology
Humans
Neovascularization, Pathologic diagnosis
Neovascularization, Pathologic drug therapy
Neovascularization, Pathologic metabolism
Angiogenesis Inhibitors therapeutic use
Antineoplastic Agents therapeutic use
Brain Neoplasms drug therapy
Glioblastoma drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1557-3265
- Volume :
- 20
- Issue :
- 22
- Database :
- MEDLINE
- Journal :
- Clinical cancer research : an official journal of the American Association for Cancer Research
- Publication Type :
- Review
- Accession number :
- 25398844
- Full Text :
- https://doi.org/10.1158/1078-0432.CCR-14-0834