Validation of a deep learning-based AI model for breast cancer risk stratification in postmenopausal ER+/HER2-breast cancer patients




Pouplier, Sandra Sinius; Sharma, Abhinav; Ruusuvuori, Pekka; Hartman, Johan; Jensen, Maj-Britt; Ejlertsen, Bent; Rantalainen, Mattias; Lænkholm, Anne-Vibeke

PublisherElsevier

2026

 Breast

104671

85

0960-9776

1532-3080

DOIhttps://doi.org/10.1016/j.breast.2025.104671

https://doi.org/10.1016/j.breast.2025.104671

https://research.utu.fi/converis/portal/detail/Publication/505986384



Background

Breast cancer prognostication is crucial for treatment decisions, and the Nottingham Histologic Grade (NHG) system is widely used. However, NHG suffers from interobserver variability, and its division into three risk groups leaves the intermediate group (comprising ∼50 % of patients) overrepresented, making individualized treatment planning challenging as prognosis within this group differ widely.

Objectives

This study aimed to validate the prognostic value of Stratipath's low and high-risk categories and five risk groups and compare NHG performance with the Stratipath deep-learning-based model.

Methods

We analyzed clinical data from 2466 postmenopausal, ER+/HER2-breast cancer patients who did not receive chemotherapy according to guidelines at that time. The NHG and Stratipath models were compared using concordance index and hazard ratios (HR) for distant recurrence (DR), with time to any recurrence (TR) and overall survival (OS) as secondary endpoints.

Results

The Stratipath five-risk group model showed similar performance to the NHG-system in predicting DR (c-index 0.71 vs. 0.72). HR for DR for Stratipath risk groups 2, 3, 4, and 5 were 1.91 (95 % CI: 1.17–3.13), 2.63 (95 % CI: 1.63–4.24), 3.18 (95 % CI: 2.00–5.07), and 3.25 (95 % CI: 2.00–5.28), respectively (p < 0.0001). In the NHG 2 subgroup, Stratipath Breast retained prognostic value for DR (HR for groups 3–5 vs. group 1: 1.73–1.85; p = 0.05), with a c-index of 0.71.

Conclusions

The Stratipath AI model performs similarly to the NHG system. Further prospective validation of the clinical benefits of differentiating Stratipath risk groups 2 and 3 in treatment strategies would be valuable.


This work was supported by the Innovation Fund Denmark, the Danish Cancer Research Fund, the Nordic Cancer Union, the Region Zealand Health Research Fund, and a Region Zealand PhD stipend. The funding sources had no role in the study design, data collection, analysis or interpretation, manuscript preparation, or the decision to submit the article for publication.


Last updated on 26/01/2026 05:20:18 PM