# Inferring Clinically Relevant Molecular Subtypes of Pancreatic Cancer from Routine Histopathology Using Deep Learning

## TL;DR

This paper introduces PanSubNet, a deep learning model that predicts molecular subtypes of pancreatic cancer from routine histology slides, enabling faster and more accessible precision oncology.

## Contribution

PanSubNet is a novel interpretable deep learning framework that predicts PDAC molecular subtypes from H&E slides, avoiding the need for RNA sequencing.

## Key findings

- PanSubNet achieved 88.5% AUC in internal validation and 84.0% AUC in external validation for molecular subtype prediction.
- The model preserves prognostic stratification and aligns with transcriptomic programs and DNA repair signatures.
- PanSubNet's predictions are associated with established differentiation markers and transcriptional states.

## Abstract

Molecular subtyping of pancreatic ductal adenocarcinoma (PDAC) into basal-like and classical has established prognostic and predictive value. However, its use in clinical practice is limited by cost, turnaround time, and tissue requirements, thereby restricting its application in the management of PDAC. We introduce PanSubNet (PANcreatic SUBtyping NETwork), an interpretable deep learning framework that predicts therapy-relevant molecular subtypes directly from standard hematoxylin and eosin (H&E)-stained whole-slide images.

PanSubNet was developed using data from 1,055 patients across two multi-institutional cohorts (PANCAN, n = 846; TCGA, n = 209) with paired histology and RNA sequencing data. Ground-truth labels were derived using the validated Moffitt 50-gene signature refined by GATA6 expression. The model employs dual-scale architecture that fuses cellular-level morphology with tissue-level architecture, leveraging attention mechanisms for multi-scale representation learning and transparent feature attribution.

On internal validation within PANCAN using five-fold cross-validation, PanSubNet achieved mean area under the receiver operating characteristic curve (AUC) of 88.5% in high-confidence cases, with balanced sensitivity and specificity. External validation on the independent TCGA cohort without fine-tuning demonstrated robust generalizability (AUC 84.0%). PanSubNet preserved and, in metastatic disease, strengthened prognostic stratification compared to RNA-seq–based labels. Prediction uncertainty linked to intermediate transcriptional states, not classification noise. Model predictions are aligned with established transcriptomic programs, differentiation markers, and DNA damage repair signatures.

By enabling rapid, cost-effective molecular stratification from routine H&E-stained slides, PanSubNet offers a clinically deployable and interpretable tool for genetic subtyping. We are gathering data from two institutions to validate and assess real-world performance, supporting integration into digital pathology workflows and advancing precision oncology for PDAC.