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Abstract #3975

Tumour mechanics and vascular fractality quantification via MR-Elastography in the context of liver metastasis from colorectal cancer

Asma Boumaza1, Gabrielle Mangin2, Jake Penney3,4, Giacomo Annio2, Samira Laouirem1, Miguel Albuquerque5, Valerie Vilgrain1,6, Valerie Paradis1,6, and Ralph Sinkus4,7
1INSERM UMRS1149 - Centre de Recherche sur l'Inflammation, University Paris, Paris, France, 2INSERM UMRS1148 - Laboratory for Vascular Translational Science, University Paris, Paris, France, 3siemens-healthineers, Paris, France, 4INSERM UMRS1148 - Laboratory for Vascular Translational Science, University Paris, paris, France, 5Assistance publique - Hôpitaux de Paris, Paris, France, 6Assistance publique - Hôpitaux de Paris, paris, France, 7School of Biomedical Engineering and Imaging Sciences, King’s College London, London, United Kingdom

Synopsis

Keywords: Biomarkers, Vessels, Liver, tumor, biomechanics, Elastography

Motivation: Colorectal cancer is a major global cause of cancer-related deaths, often metastasizing to the liver. Standard treatment includes chemotherapy and anti-angiogenic therapy. Quantifying therapy efficacy remains a clinical challenge.

Goal(s): We explore multifrequency MR-Elastography (MRE) for assessing vascular organization, using a murine liver metastasis model correlated with histopathology.

Approach: The study used MRE imaging of murin liver metastasis model and the corresponding histopathology to analyze vascular organization (fractal dimension), by measuring Hurst index (H-index).

Results: The H-index differs significantly between tumor and healthy liver tissue, with normal vasculature displaying a lower H-index compared to the tumoral tissue.

Impact: Our in vivo elastography study demonstrates the organization of the vascular network by matching with histological findings. This innovative approach paves the way for non-invasive evaluation of treatments targeting tumor vessels, such as bevacizumab or FOLFOX.

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