Abstract PO-067: AI and CT-radiomics as a tool for breast cancer prognosis and radiomics-gene isolation: Activated MET induced mammary carcinoma as a model

Triple-negative breast cancer (TNBC) is a type of aggressive breast cancer lacking the expression of estrogen receptors (ER), progesterone receptors (PR), and human epidermal growth factor receptor-2 (HER-2). TNBC represents a heterogeneous subtype of breast cancer that carries a poorer prognosis. There remains a need to identify novel driver and modifier genes of TNBC, representing targets to treat the disease. MET tyrosine kinase is the receptor for hepatocyte growth factor/scatter factor (HGF/SF). MET overexpression and constitutively activated mutation promotes tumor growth, cell motility and metastases, making MET an ideal target for anti-metastatic precision therapy. In mice carrying MET constitutive activation mutation (METmut), the gene initiates tumorigenicity associated with inherited driver modifier genes (IDMGs). The Collaborative Cross (CC) animal model consists of recombinant inbred lines generated by reciprocal crosses between numerous founder lines. It is a reference to apply genetic traits mapping with high-resolution phenotypes such as radiomic features. In this study, we established a new machine learning prognostic model of overall survival (OS) of METmut-induced mammary carcinoma. QTL (Quantitative Trait Locus) mapping analysis was used to identify candidate genes that may contribute to intra-tumor heterogenicity and OS. Two CT images cohorts were included: METmut-FVB/N and METmut-CC mice that developed mammary carcinoma (n=13 and n=15, respectively). Each segmented tumor was divided into 3D cubes, and radiomic features were extracted from each cube using a novel in-house tool. We performed Principle Component Analysis (PCA) and cluster analysis (k-means) on the radiomic features to produce cube cluster groups with similar radiomic characteristics, such as tumor region intensity and morphology. We then assessed each cluster group9s proportion per tumor – the cluster proportion - as a radiomic phenotype for QTL. QTL analysis identified loci in chromosomes #6 and #15 that code for new radiomics morphological candidate genes that may alter MET signaling and reduce OS. To analyze tumor heterogenicity, median and standard deviation of cubes PCA values were calculated per tumor and used as covariates in Cox regression against OS. Four out of the eight covariates were significantly correlated with OS (P Citation Format: Ilan Tsarfaty, Eran Dotan, Michal Bloom, Judith Horev, Fuad Iraqi. AI and CT-radiomics as a tool for breast cancer prognosis and radiomics-gene isolation: Activated MET induced mammary carcinoma as a model [abstract]. In: Proceedings of the AACR Virtual Special Conference on Artificial Intelligence, Diagnosis, and Imaging; 2021 Jan 13-14. Philadelphia (PA): AACR; Clin Cancer Res 2021;27(5_Suppl):Abstract nr PO-067.