A. J. Allphin,1 Y. Mowery,1 K. J. Lafata,1,2 D. P. Clark,1 A. Basil,1 Rico Castillo,1 M. D. Holbrook,1 K. B. Ghaghada,3,4 C. T. Badeahttps://orcid.org/0000-0002-1850-25221
1Duke Univ. Medical Ctr. (United States) 2Duke Univ. (United States) 3Texas Children's Hospital (United States) 4Baylor College of Medicine (United States)
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The purpose of this study was to investigate if radiomic analysis based on spectral micro-CT with nanoparticle contrastenhancement can differentiate tumors based on tumor-infiltrating lymphocyte (TIL) burden. High mutational load transplant soft tissue sarcomas were initiated in Rag2+/- and Rag2-/- mice to model varying TIL burden. Mice received radiation therapy (20 Gy) to the tumor-bearing hind limb and were injected with a liposomal iodinated contrast agent. Five days later, animals underwent conventional micro-CT imaging using an energy integrating detector (EID) and spectral micro-CT imaging using a photon-counting detector (PCD). Tumor volumes, and iodine uptakes were measured. The radiomic features (RF) were grouped into feature-spaces corresponding to EID, PCD, and spectral decomposition images. RFs were ranked to reduce redundancy and increase relevance based on TIL burden. A leave one out strategy was used to assess separation using a neural network classifier. Tumor iodine concentration was the only significantly different conventional tumor metric between Rag2+/- (TILs present) and Rag2-/- (TIL-deficient) tumors. RFs further enabled differentiation between Rag2+/- and Rag2-/- tumors. The PCD-derived RFs provided the highest accuracy (0.84) followed by decomposition-derived RFs (0.78) and the EID-derived RFs (0.65). Such non-invasive approaches could aid in tumor stratification for cancer therapy studies.
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A. J. Allphin, Y. Mowery, K. J. Lafata, D. P. Clark, A. Basil, Rico Castillo, M. D. Holbrook, K. B. Ghaghada, C. T. Badea, "Spectral micro-CT and radiomic analysis for classification of tumors based on lymphocytic burden in cancer therapy studies," Proc. SPIE 12036, Medical Imaging 2022: Biomedical Applications in Molecular, Structural, and Functional Imaging, 120361H (4 April 2022); https://doi.org/10.1117/12.2611519