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Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
The role of anti-angiogenesis in non-small-cell lung cancer: an update
Liza C Villaruz1, Mark A Socinski
1Lung Cancer Program, University of Pittsburgh Cancer Institute, 5150 Centre Avenue, 5th Floor Cancer Pavilion, Room 567, Pittsburgh, PA, 15232, USA, villaruzl@upmc.edu.
Abstract:
Recognition of the vascular endothelial growth factor (VEGF) pathway as a key mediator of angiogenesis has led to the clinical study of several VEGF and VEGF receptor (VEGFR) targeted therapies in non-small-cell lung cancer (NSCLC). These targeted therapies include neutralizing antibodies to VEGF (bevacizumab and aflibercept) and VEGFR-2 (ramucirumab) and tyrosine kinase inhibitors (TKIs) with selectivity for the VEGFRs. Bevacizumab and ramucirumab are associated with survival advantages in the treatment of advanced NSCLC: bevacizumab in the first-line setting in combination with carboplatin/paclitaxel and ramucirumab in combination with docetaxel in the second-line setting. The VEGFR-2 TKIs have been associated with responses and improved progression-free survival in selected NSCLC settings; however, this level of activity has thus far been insufficient to confer significant survival advantages. This review will focus on the current state of VEGF targeted therapies in NSCLC.
Insights
Targeted therapies blocking vascular endothelial growth factor (VEGF) show promise in non-small-cell lung cancer (NSCLC). Bevacizumab and ramucirumab improve survival, while VEGFR-2 TKIs offer responses but not significant survival benefits.
Area of Science:
- Oncology
- Pharmacology
Background:
- Vascular endothelial growth factor (VEGF) pathway is crucial for angiogenesis.
- Targeted therapies against VEGF and its receptors (VEGFRs) are investigated for non-small-cell lung cancer (NSCLC).
Purpose of the Study:
- To review the current status of VEGF-targeted therapies in NSCLC treatment.
- To evaluate the efficacy and survival benefits of different VEGF-targeted agents.
Main Methods:
- Review of clinical studies on VEGF and VEGFR-targeted therapies in NSCLC.
- Analysis of data on neutralizing antibodies (bevacizumab, aflibercept, ramucirumab) and tyrosine kinase inhibitors (TKIs).
Main Results:
- Bevacizumab and ramucirumab demonstrate survival advantages in advanced NSCLC when used in specific treatment settings.
- VEGFR-2 TKIs show responses and improved progression-free survival in certain NSCLC cases, but without significant survival gains.
Conclusions:
- VEGF-targeted therapies, particularly bevacizumab and ramucirumab, offer survival benefits in NSCLC.
- Further research is needed to optimize the use of VEGFR-2 TKIs for improved patient survival in NSCLC.
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