Abstract

Breast cancer, the most common female malignancy, is highly heterogeneous, manifesting as different molecular subtypes. It is clinically important to distinguish between these molecular subtypes due to marked differences in prognosis, treatment and survival outcomes. In this study, we first performed convex analysis of mixtures (CAM) analysis on both intratumoral and peritumoral regions in DCE-MRI to generate multiple heterogeneous regions. Then, we developed a vision transformer (ViT)-based DL model and performed network architecture search (NAS) to evaluate all the combination of different heterogeneous regions for predicting molecular subtypes of breast cancer. Experimental results showed that the input plasma from both peritumoral and intratumoral regions, and the fast-flow kinetics from intratumoral regions were critical for predicting different molecular subtypes, achieving an area under receiver operating characteristic curve (AUROC) value of 0.66-0.68.Clinical Relevance- This study reduces the redundancy in multiple heterogeneous subregions and supports the precise prediction of molecular subtypes, which is of potential importance for the medicine care and treatment planning of patients with breast cancer.

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