Block Graph Neural Networks for tumor heterogeneity prediction

TL;DR

This paper introduces Block Graph Neural Networks (BGNN) trained on artificially generated tumor data to predict tumor heterogeneity, aiming to improve classification accuracy beyond traditional methods.

Contribution

The paper presents a novel BGNN approach, new tumor features, and data generation methods based on tumor evolution models for heterogeneity prediction.

Findings

Achieved 89.67% accuracy on artificial data

Demonstrated effectiveness of new features and BGNN in heterogeneity prediction

Highlighted potential of combining traditional grading with molecular markers

Abstract

Accurate tumor classification is essential for selecting effective treatments, but current methods have limitations. Standard tumor grading, which categorizes tumors based on cell differentiation, is not recommended as a stand-alone procedure, as some well-differentiated tumors can be malignant. Tumor heterogeneity assessment via single-cell sequencing offers profound insights but can be costly and may still require significant manual intervention. Many existing statistical machine learning methods for tumor data still require complex pre-processing of MRI and histopathological data. In this paper, we propose to build on a mathematical model that simulates tumor evolution (O\.{z}a\'{n}ski (2017)) and generate artificial datasets for tumor classification. Tumor heterogeneity is estimated using normalized entropy, with a threshold to classify tumors as having high or low heterogeneity. Our contributions are threefold: (1) the cut and graph generation processes from the artificial data, (2) the design of tumor features, and (3) the construction of Block Graph Neural Networks (BGNN), a Graph Neural Network-based approach to predict tumor heterogeneity. The experimental results reveal that the combination of the proposed features and models yields excellent results on artificially generated data ($89.67\%$ accuracy on the test data). In particular, in alignment with the emerging trends in AI-assisted grading and spatial transcriptomics, our results suggest that enriching traditional grading methods with birth (e.g., Ki-67 proliferation index) and death markers can improve heterogeneity prediction and enhance tumor classification.