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Abstract #1930

Repeatability of quantitative MRI protocol of hypoxia, cellularity, and perfusion for habitat imaging in a murine glioma model

Ayesha Das1, David A Hormuth II1,2, Jack Virostko2,3,4, and Thomas Yankeelov1,2,4,5,6,7
1Biomedical Engineering, University of Texas at Austin, Austin, TX, United States, 2Oden Institute for Computational Science and Engineering, University of Texas at Austin, Austin, TX, United States, 3Diagnostic Medicine, Dell Medical School, Austin, TX, United States, 4Livestrong Cancer Institutes, Dell Medical School, Austin, TX, United States, 5Department of Diagnostic Medicine, Dell Medical School, Austin, TX, United States, 6Department of Oncology, Dell Medical School, Austin, TX, United States, 7Department of Imaging Physics, MD Anderson Cancer Center, Houston, TX, United States

Synopsis

Keywords: Preclinical Image Analysis, Quantitative Imaging, preclinical, cancer

Motivation: Hypoxia in heterogeneous tumors raises radiotherapy resistance, worsening patient outcomes. A reliable, quantifiable MRI protocol could help address this challenge.

Goal(s): We would like to develop a quantifiable and repeatable MRI protocol to measure cellularity, perfusion, and hypoxia to capture tumor heterogeneity in preclinical glioma models.

Approach: Animals with brain tumors underwent test-retest MRI sessions, after which the MRI data was combined to define subregions with distinct physiological characteristics.

Results: The repeatability values are within the values previously reported for murine studies of cancer. Our image-derived quantification of hypoxia, cellularity, and perfusion can capture tumor heterogeneity at the ROI level.

Impact: We have presented updated findings on the repeatability of our quantitative and multiparametric MRI protocol for identifying tumor habitats. Our image-derived quantification of hypoxia, cellularity, and perfusion can capture tumor heterogeneity at the ROI level.

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