Pathology-genomic fusion via biologically informed cross-modality graph learning for survival analysis

TL;DR

This paper introduces a biologically informed graph neural network model that effectively fuses histology images and genomic data for improved cancer survival prediction, providing interpretability through attention visualization.

Contribution

It proposes a novel multi-modal fusion framework using a heterogeneous graph neural network guided by biological prior knowledge, enhancing survival analysis accuracy.

Findings

Outperforms existing unimodal and multi-modal models on TCGA datasets.

Provides interpretable insights via attention heatmaps and gene importance analysis.

Demonstrates effectiveness across multiple cancer types.

Abstract

The diagnosis and prognosis of cancer are typically based on multi-modal clinical data, including histology images and genomic data, due to the complex pathogenesis and high heterogeneity. Despite the advancements in digital pathology and high-throughput genome sequencing, establishing effective multi-modal fusion models for survival prediction and revealing the potential association between histopathology and transcriptomics remains challenging. In this paper, we propose Pathology-Genome Heterogeneous Graph (PGHG) that integrates whole slide images (WSI) and bulk RNA-Seq expression data with heterogeneous graph neural network for cancer survival analysis. The PGHG consists of biological knowledge-guided representation learning network and pathology-genome heterogeneous graph. The representation learning network utilizes the biological prior knowledge of intra-modal and inter-modal data associations to guide the feature extraction. The node features of each modality are updated through attention-based graph learning strategy. Unimodal features and bi-modal fused features are extracted via attention pooling module and then used for survival prediction. We evaluate the model on low-grade gliomas, glioblastoma, and kidney renal papillary cell carcinoma datasets from the Cancer Genome Atlas (TCGA) and the First Affiliated Hospital of Zhengzhou University (FAHZU). Extensive experimental results demonstrate that the proposed method outperforms both unimodal and other multi-modal fusion models. For demonstrating the model interpretability, we also visualize the attention heatmap of pathological images and utilize integrated gradient algorithm to identify important tissue structure, biological pathways and key genes.