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Assessing tumor angiogenesis using macromolecular MR imaging contrast media
1Department of Radiology, University of California San Francisco 94143-0628, USA.
Journal of Magnetic Resonance Imaging : JMRI
|January 1, 1997
Summary
Macromolecular contrast medium-enhanced MRI can detect suppressed tumor microvascular permeability after anti-VEGF antibody treatment. This MRI technique shows potential for grading tumor angiogenesis and monitoring anti-angiogenesis therapies.
Area of Science:
- Oncology
- Radiology
- Biomedical Engineering
Background:
- Macromolecular contrast medium (MMCM)-enhanced MRI estimates tumor microvascular characteristics, correlating with histologic microvascular density.
- Vascular endothelial growth factor (VEGF) is a key stimulator of angiogenesis.
- MMCM-enhanced MRI can assess the acute effects of anti-VEGF therapy on tumor vasculature.
Purpose of the Study:
- To investigate the acute tumor microvascular effects of antibody-mediated inhibition of VEGF using MMCM-enhanced MRI.
- To quantify changes in tumor microvascular permeability and blood volume following anti-VEGF treatment.
Main Methods:
- Athymic rats with human breast carcinoma xenografts were imaged using MMCM-enhanced MRI (albumin-Gd-DTPA30).
- Imaging was performed before and 24 hours after a single dose of anti-VEGF antibody.
- A bidirectional two-compartment kinetic model analyzed changes in longitudinal relaxivity (ΔR1) to estimate fractional blood volume (fBV) and permeability-surface area product (PS).
Main Results:
- A significant decrease in tumor PS was observed 24 hours post-anti-VEGF antibody treatment (P < 0.05).
- No significant change in tumor fractional blood volume (fBV) was detected.
- MMCM-enhanced MRI successfully detected and quantified the suppression of tumor microvascular permeability induced by anti-VEGF antibody.
Conclusions:
- MMCM-enhanced MRI can effectively monitor the anti-angiogenic effects of VEGF inhibition by quantifying changes in tumor microvascular permeability.
- This MRI technique holds promise for clinical applications in grading tumor angiogenesis and monitoring anti-angiogenesis interventions.