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Published on: October 27, 2014
Bevacizumab and ovarian cancer
Shinya Sato1, Hiroaki Itamochi
1Department of Obstetrics and Gynecology, Tottori University School of Medicine, Yonago, Tottori, Japan.
Purpose Of Review:
Vascular endothelial growth factor (VEGF), one of the major pathways involved in tumor angiogenesis, is often overexpressed in epithelial ovarian cancer (EOC), and therefore an attractive target for therapy. This review aims to evaluate the rationale for targeting angiogenic pathways by the usage of the anti-VEGF agent bevacizumab in EOC.
Recent Findings:
Bevacizumab monotherapy has been shown to be effective in the treatment of EOC with response rate of 16-21% in phase II trials. In phase III trials, patients with advanced EOC who received combination chemotherapy (paclitaxel + carboplatin) plus bevacizumab with maintenance bevacizumab had significantly longer progression-free survival than those who received chemotherapy alone, but did not prolong overall survival. The most common grade 3/4 adverse events of bevacizumab monotherapy include hypertension and proteinuria, while heavily pretreated patients were at increased risk of bowel perforation. The addition of bevacizumab to the standard chemotherapy in patients with advanced EOC may not be cost-effective.
Summary:
Bevacizumab has significant activity and is the most promising drug in EOC. However, understanding of its unique adverse events and identification of predictive biomarkers of bevacizumab response are necessary in order to select patients most likely to benefit from this therapy.
Insights
Bevacizumab shows promise in treating epithelial ovarian cancer (EOC) by targeting vascular endothelial growth factor (VEGF). While improving progression-free survival, it did not extend overall survival and has associated adverse events requiring further study.
Area of Science:
- Oncology
- Pharmacology
Background:
- Vascular endothelial growth factor (VEGF) is a key pathway in tumor angiogenesis and is frequently overexpressed in epithelial ovarian cancer (EOC).
- VEGF is a validated therapeutic target in various cancers, including EOC.
Purpose of the Study:
- To review the rationale for targeting angiogenic pathways with bevacizumab, an anti-VEGF agent, in epithelial ovarian cancer.
- To evaluate the efficacy, safety, and cost-effectiveness of bevacizumab in EOC treatment.
Main Methods:
- Review of phase II and III clinical trials evaluating bevacizumab in EOC.
- Analysis of response rates, progression-free survival, overall survival, and adverse events.
Main Results:
- Bevacizumab monotherapy demonstrated response rates of 16-21% in phase II trials.
- Phase III trials showed bevacizumab plus chemotherapy significantly improved progression-free survival but not overall survival in advanced EOC.
- Common adverse events include hypertension and proteinuria; bowel perforation risk increased in heavily pretreated patients. Cost-effectiveness remains a concern.
Conclusions:
- Bevacizumab exhibits significant activity and is a promising agent for EOC.
- Further understanding of bevacizumab's adverse events and identification of predictive biomarkers are crucial for patient selection.
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