Journal
JOURNAL OF MAGNETIC RESONANCE IMAGING
Volume 22, Issue 4, Pages 511-519Publisher
WILEY
DOI: 10.1002/jmri.20387
Keywords
magnetic resonance imaging; human breast cancer xenograft; vascular endothelial growth factor receptor tyrosine kinase inhibitor; contrast media; endothelial permeability
Funding
- NCI NIH HHS [CA 82923, CA 069587] Funding Source: Medline
Ask authors/readers for more resources
Purpose: To investigate the heterogeneity in the angiogenic response of a human breast cancer xenograft to a novel vascular endothelial growth factor (VEGF)-receptor tyrosine kinase inhibitor, AG-013736, using dynamic contrast-enhanced MR imaging (DCE-MRI). Materials and Methods: Changes in pharmacokinetic parameters in a seven-day interval were compared between AG-treated and control groups, using Gd-DTPA and albumin-(Gd-DTPA)(30). A voxel-by-voxel analysis was performed to produce parametric spatial pharmacokinetic parametric maps and histograms. Histogram segmentation was used to quantify the heterogeneity in tumor response to therapy, and compared with conventional descriptive measures of distribution in terms of their capacity to separate control from AG-treated tumors. Results: The albumin- (Gd-DTPA)(30) endothelial transfer constant, K-ps, showed changes with AG-013736 treatment and tumor growth. The changes were highly heterogeneous for individual segments of the histogram with different K-ps values, and the overall patterns in which the frequency distribution changed differed significantly between the two groups. A change in the number of voxels with K-ps rangingfrom 0.03 to 0.14 mL/min/(100 mL tissue) was the most sensitive variable for separating control from AG-treated tumors (P = 0.0008). Parametric maps of the kinetic parameters also showed spatial heterogeneity in tumor response to treatment. The K-ps maps depicted rapid development of central necrosis as a result of AG-013736 treatment. Maps of upsilon(p) demonstrated a marked increase at peripheral regions of necrotic areas. Similar trends were noted in the Gd-DTPA rate constant K-trans distribution. Conclusion: This study demonstrates the value of histogram analysis of maps of pharmacokinetic parameters for assessing heterogeneity in tumor response to antiangiogenic therapy. Changes in the number of voxels within certain segments of the K-ps histogram were the most sensitive variable for separating control from AG-treated tumors.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available