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Updated: Jul 15, 2026

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
VEGF-targeted cancer therapy strategies: current progress, hurdles and future prospects
Dan G Duda1, Tracy T Batchelor, Christopher G Willett
1Steele Laboratory, Department of Radiation Oncology, Massachusetts General Hospital, 100 Blossom Street, Cox-734, Boston, MA 02114, USA.
Abstract:
Despite setbacks, the clinical development of antiangiogenic agents has accelerated remarkably over the past 3-4 years. Consequently, there are currently three direct inhibitors of the VEGF pathway approved for use in cancer therapy. Other agents that block the VEGF pathway are in advanced stages of clinical development and have shown promising results. With these exciting developments come crucial questions regarding the use of these new molecular-targeted agents, alone or in combination with standard cytotoxic or targeted agents. Importantly, the mechanisms of action of anti-VEGF therapy remain unknown. Here, we discuss several potential mechanisms of action such as tumor vascular normalization, bone marrow-derived cell recruitment blockade and cytostatic effects of anti-VEGF therapy. We review the current progress, the major stumbling blocks and the future directions for anti-cancer therapy using anti-VEGF agents, emphasizing clarification of the underlying molecular mechanisms of action and biomarker identification and validation.
Insights
Anti-VEGF therapies show promise in cancer treatment, with approved agents and ongoing development. Further research is crucial to understand their mechanisms and identify biomarkers for effective use.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Clinical development of antiangiogenic agents, particularly vascular endothelial growth factor (VEGF) inhibitors, has accelerated significantly.
- Three direct VEGF pathway inhibitors are currently approved for cancer therapy, with others in advanced clinical development showing promising results.
Purpose of the Study:
- To discuss the crucial questions surrounding the use of novel molecular-targeted anti-VEGF agents in cancer therapy.
- To explore potential mechanisms of action for anti-VEGF therapy, including tumor vascular normalization, blockade of bone marrow-derived cell recruitment, and cytostatic effects.
- To review the progress, challenges, and future directions in anti-cancer therapy utilizing anti-VEGF agents, focusing on clarifying molecular mechanisms and validating biomarkers.
Main Methods:
- Review of current clinical development progress for antiangiogenic agents.
- Discussion of potential mechanisms of action for anti-VEGF therapy.
- Analysis of challenges and future directions in the field.
Main Results:
- Significant acceleration in the clinical development of antiangiogenic agents.
- Approval of three direct VEGF pathway inhibitors for cancer therapy.
- Promising results from other VEGF pathway inhibitors in advanced clinical development.
Conclusions:
- Clarification of the underlying molecular mechanisms of action for anti-VEGF therapy is essential.
- Identification and validation of biomarkers are critical for optimizing the use of anti-VEGF agents.
- Further research is needed to address the optimal use of these agents, alone or in combination therapies.
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