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Abstract #3835

Diffusion and contrast-enhancement MRI phenotypes predict immune cell infiltration in brain metastases

Francesco Sanvito1,2, Sonoko Oshima1,2, Eileen Shiuan3, Lu Sun4, Nicholas S Cho1,2, Asher Kim5, Noriko Salamon2, Benjamin M Ellingson1,2, Robert Prins4, Won Kim4, and Jingwen Yao1,2
1Brain Tumor Imaging Laboratory (BTIL), Department of Radiological Sciences, University of California Los Angeles, Los Angeles, CA, United States, 2Department of Radiological Sciences, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States, 3Division of Hematology/Oncology, Department of Medicine, University of California Los Angeles, Los Angeles, CA, United States, 4Department of Neurosurgery, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States, 5Department of Bioengineering, Henry Samueli School of Engineering and Applied Science, University of California Los Angeles, Los Angeles, CA, United States

Synopsis

Keywords: Tumors (Post-Treatment), Treatment

Motivation: Immune checkpoint inhibitors (ICIs) can promote immune cell infiltration and increase anti-tumoral immune response in brain metastases (BM). Imaging proxies of immune infiltration would facilitate ICI-response monitoring in BM.

Goal(s): To test whether the combined assessment of diffusion and contrast-enhancement MRI phenotypes can provide insights into microscopic immune infiltration.

Approach: We studied the associations of diffusion and contrast-enhancement MRI phenotypes with histological immune cell infiltration and with ICI-treatment status

Results: Correlation analysis showed that high diffusivity and pronounced contrast-enhancement were positively associated with increased immune cell infiltration and were more likely observed in ICI-treated lesions.

Impact: Immune checkpoint inhibitors (ICIs) can promote immune cell infiltration and increase anti-tumoral immune response in brain metastases (BM). Diffusion and contrast-enhancement MRI phenotypes provide potential imaging biomarkers to non-invasively monitor tissue changes related to anti-tumoral immune response following ICIs.

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Keywords