A spatial AI-based biomarker with independent prognostic value in early low- and intermediate- risk breast cancer
Preprint
Abstract
Background: Patients with ER-positive/HER2-negative early breast cancer of low or intermediate grade are generally considered to have a favourable prognosis, yet a number will recur. This risk is poorly captured by standard clinicopathological factors. AI-based medical devices for whole slide image (WSI) analyses used for risk-stratification often predict on slide-level thereby overlooking spatial localisation of the biomarkers. We hypothesise that the spatial distribution of a previously reported AI-based marker provides independent prognostic value beyond its global score. Patients and Methods: This Swedish multicentre cohort study includes 6106 patients with primary invasive breast cancer: 3078 from the Stockholm region (training) and 3028 from Skåne (independent test). Tile-level high-grade morphology scores were generated with ViT_DG, a vision-transformer adaptation of DeepGrade, and the presence of clusters of high-risk tiles localised at the invasive tumour front was defined as a binary biomarker. Primary analyses were pre-specified in the ER-positive/HER2-negative/lymph-node-negative and Grade 1-2 subgroup. Association with breast-cancer recurrence-free interval (BCRFI) and distant metastasis were assessed using multivariable Cox proportional hazards models (HR). Results: In the primary subgroup (n=1536 training; n=1403 test), tumour front clusters were present in 37% and 39% of patients. Cluster-positive status was associated with a 2.30-fold increased risk in the external test. Cluster-negative patients achieved a 10-year BCRFI of 95.3%, equivalent to Grade 1 patients and better than Grade 2 (92.4%), whereas cluster-positive patients (90.2%) did worse than the Grade 3 reference. The association was retained in patients classified as low-risk by ViT_DG (test set multivariable HR 2.86), identifying high-risk patients not captured by the global score. Conclusions: The absence of high-risk morphology clusters at the tumour front is an independent prognostic indicator, identifying a low-risk group independently of the global AI biomarker classification. More broadly, preserving the spatial distribution of AI-derived predictions enables prognostic stratification beyond slide-level aggregation. ClinicalTrials.gov identifier: NCT02306096Keywords
Funding Information
- AstraZeneca
This publication has 35 references indexed in Scilit:
- Validation of a deep learning-based AI model for breast cancer risk stratification in postmenopausal ER+/HER2-breast cancer patientsThe Breast, 2025
- Prognostic value of tumor-infiltrating lymphocytes (TILs) in Luminal breast cancer: A novel computational method for assessing TILs abundance and spatial distribution patternsThe Breast, 2025
- Early breast cancer: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-upAnnals of Oncology, 2023
- Understanding breast cancer complexity to improve patient outcomes: The St Gallen International Consensus Conference for the Primary Therapy of Individuals with Early Breast Cancer 2023Annals of Oncology, 2023
- Transcriptional intra-tumour heterogeneity predicted by deep learning in routine breast histopathology slides provides independent prognostic informationEuropean Journal of Cancer, 2023
- Improved breast cancer histological grading using deep learningAnnals of Oncology, 2022
- High tumor budding stratifies breast cancer with metastatic propertiesBreast Cancer Research and Treatment, 2015
- The prognostic value of tumor budding in invasive breast cancerPathology - Research and Practice, 2013
- Epithelial-Mesenchymal Transitions in Development and DiseaseCell, 2009
- Index for rating diagnostic testsCancer, 1950