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Tumor Treating Field Therapy in Combination with Bevacizumab for the Treatment of Recurrent Glioblastoma
Published on: October 27, 2014
Evolving strategies: future treatment of glioblastoma
1University of Washington, Fred Hutchinson Cancer Research Center, Seattle Cancer Care Alliance, 825 Eastlake Ave E, POB 19023, MS G4-940, Seattle, WA 98109-1023, USA. chambemc@uw.edu
Abstract:
Despite recent advances, there remains an unmet need for more effective treatments for newly diagnosed and recurrent glioblastoma (GBM). While currently available alkylator-based and antiangiogenic agents provide some efficacy, novel antiangiogenic and antiglioma treatments that provide enhanced efficacy with improvements in overall survival, the potential to overcome drug resistance and decreased treatment-related toxicity are still needed. Although VEGF-directed angiogenesis is critical during GBM pathogenesis, alternative proangiogenic and glioma-promoting pathways also play a key role in tumor progression. This article reviews the limitations of current GBM treatment, the importance of angiogenic signaling pathways in GBM pathogenesis and the preliminary results of novel antiangiogenic-targeted treatments being evaluated in GBM. Therapies that inhibit multiple glioma signaling pathways, including angiogenesis, have the possibility for further improving outcome in GBM and may represent the best option for increasing overall survival.
Insights
New treatments are needed for glioblastoma (GBM). Novel therapies targeting multiple pathways, including angiogenesis, show promise for improving survival and overcoming drug resistance in GBM patients.
Area of Science:
- Neuro-oncology
- Cancer biology
- Translational medicine
Background:
- Glioblastoma (GBM) remains a challenging brain tumor with limited effective treatments.
- Current therapies like alkylators and antiangiogenic agents offer some benefit but do not overcome resistance or significantly improve survival.
- VEGF-directed angiogenesis is crucial, but other proangiogenic pathways also drive GBM progression.
Purpose of the Study:
- To review current glioblastoma treatment limitations.
- To highlight the role of angiogenic signaling in GBM pathogenesis.
- To discuss preliminary results of novel antiangiogenic therapies for GBM.
Main Methods:
- Literature review of current GBM treatments.
- Analysis of the role of angiogenesis and other signaling pathways in GBM.
- Evaluation of emerging antiangiogenic and antiglioma treatment strategies.
Main Results:
- Existing treatments for glioblastoma have significant limitations.
- Multiple proangiogenic and glioma-promoting pathways contribute to tumor progression beyond VEGF.
- Novel therapies targeting multiple pathways, including angiogenesis, are under investigation.
Conclusions:
- Inhibiting multiple signaling pathways, particularly angiogenesis, offers a promising strategy for improving glioblastoma outcomes.
- Targeting combined pathways may overcome drug resistance and reduce toxicity.
- Multimodal therapeutic approaches hold potential for enhancing overall survival in GBM patients.
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