Evidence map›Paper›PMID 41831466›Full record

ArticleThe Lancet. Oncology2026

Deep learning on histopathological images to predict breast cancer recurrence risk and chemotherapy benefit: a multicentre, model development and validation study.

Gil Shamai, Shachar Cohen, Yoav Binenbaum, Edmond Sabo, Alexandra Cretu, Chen Mayer, Iris Barshack, Tal Goldman, Gil Bar-Sela, António Polónia and 6 more

Abstract readMulticenter StudyValidation Study
In one paragraph

Article in The Lancet. Oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

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  11. Impact of anthracyclines in genomic high-risk, node-negative, HR-positive/HER2-negative breast cancer.Annals of oncology : official journal of the European Society for Medical Oncology · 2025
    Article
  12. Immunohistochemical predictors of local recurrence in breast carcinoma: development and sensitivity validation of an IHC-based risk score.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Gil ShamaiTaub Faculty of Computer Science, Technion-Israel Institute of Technology, Haifa, Israel. Electronic address: sgils@technion.ac.il.
Shachar CohenTaub Faculty of Computer Science, Technion-Israel Institute of Technology, Haifa, Israel.
Yoav BinenbaumDana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA, USA; Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, MA, USA.
Edmond SaboDepartment of Pathology, Carmel Medical Center, Haifa, Israel; Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
Alexandra CretuDepartment of Pathology, Carmel Medical Center, Haifa, Israel.
Chen MayerInstitute of Pathology, Sheba Tel Hashomer Medical Center, Ramat-Gan, Israel.
Iris BarshackInstitute of Pathology, Sheba Tel Hashomer Medical Center, Ramat-Gan, Israel.
Tal GoldmanDepartment of Pathology, Emek Medical Center, Afula, Israel.
Gil Bar-SelaDepartment of Oncology, Emek Medical Center, Afula, Israel; Technion Integrated Cancer Center, Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
António PolóniaInstitute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal; School of Medicine and Biomedical Sciences, Fernando Pessoa University, Porto, Portugal.
Dezheng HuoDepartment of Public Health Sciences, University of Chicago, Chicago, IL, USA.
Alexander T PearsonDepartment of Medicine, University of Chicago, Chicago, IL, USA; Chan Zuckerberg Biohub Chicago, Chicago, IL, USA.
Frederick M HowardDepartment of Medicine, University of Chicago, Chicago, IL, USA.
Joseph A SparanoIcahn School of Medicine at Mount Sinai, Tisch Cancer Institute, New York, NY, USA.
Ron KimmelTaub Faculty of Computer Science, Technion-Israel Institute of Technology, Haifa, Israel; Faculty of Electrical and Computer Engineering, Technion-Israel Institute of Technology, Haifa, Israel.
Dvir AranTaub Faculty of Computer Science, Technion-Israel Institute of Technology, Haifa, Israel; Faculty of Biology, Technion-Israel Institute of Technology, Haifa, Israel.

Funding

Project-006U10CA180820 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer · 2014 to 2026
$167.6M
Statistics CoreU10CA180794 · NCI · DANA-FARBER CANCER INST · PI PAUL J CATALANO, CONSTANTINE A. GATSONIS · 2014 to 2026
$111.2M
Pilot Program CoreP30ES027792 · NIEHS · UNIVERSITY OF CHICAGO · PI Gokhan M. Mutlu, Gail S Prins · 2017 to 2026
$13.6M
Research Training in Pediatric OncologyT32CA136432 · NCI · DANA-FARBER CANCER INST · PI SCOTT A ARMSTRONG · 2009 to 2026
$7.9M
EPA EP-C-18-007NCI NIH HHS T32 CA136432NCI NIH HHS U10 CA180794NCI NIH HHS U10 CA180820NIEHS NIH HHS P30 ES027792
6 · The paper itself

Abstract

backgroundGenomic assays such as Oncotype DX have transformed adjuvant treatment selection for hormone receptor-positive, HER2-negative, early breast cancer but remain inaccessible to many patients because of high cost and logistical barriers. We aimed to develop and validate an artificial intelligence (AI) model that estimates Oncotype DX 21-gene recurrence scores directly from routine histopathology slides and clinicopathological variables.

methodsIn this multicentre, model development and validation study, a multimodal deep-learning model was trained on digital whole-slide images and clinical features using a foundation model pre-trained on 171 189 histopathology slides for predicting Oncotype DX recurrence score. We included slides from patients with hormone receptor-positive, HER2-negative, invasive breast cancers and without scanning artifacts and with at least 100 tissue tiles (1·6 mm

findingsIn the TAILORx-test set (n=2407), the AI model classified 1097 (45·6%) patients as low risk, 1021 (42·4%) as intermediate risk, and 289 (12·0%) as high risk. For identifying high genomic-risk disease (recurrence score ≥26), the area under the curve (AUC) was 0·898 (95% CI 0·879-0·913). AI-based risk stratification was prognostic for recurrence-free interval (hazard ratio 2·61 [95% CI 1·68-4·04]), distant recurrence-free interval (2·88 [1·73-4·79]), and disease-free survival (1·32 [0·92-1·89]). Chemotherapy benefit was evident in premenopausal patients classified by AI as being at high risk (0·63 [0·46-0·86]) but absent in postmenopausal patients classified by AI as being at low risk (0·94 [0·78-1·12]). 151 (31·3%) clinically high-risk postmenopausal women (by MINDACT criteria) were reclassified as low AI risk with no chemotherapy benefit. Analysis on external cohorts (5497 patients) showed that the model is transferable to new data with high generalisability (recurrence score ≥26 AUC ranging from 0·858 to 0·903).

interpretationThese findings show that AI applied to routine histopathology can serve as a practical and scalable tool for guiding chemotherapy decisions in hormone receptor-positive, HER2-negative, early breast cancer. This approach has the potential to reduce unnecessary chemotherapy and broaden access to precision oncology, particularly in resource-limited settings where genomic testing remains unavailable or unaffordable.

fundingIsrael Innovation Authority (Kamin), Zimin Institute for Artificial Intelligence Solutions in Healthcare, Israel Precision Medicine Partnership program, and Israel Cancer Research Fund.

Indexed as

Breast NeoplasmsDeep LearningNeoplasm Recurrence, LocalBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesFemaleHumansMiddle AgedPredictive Learning ModelsPredictive Value of TestsPrognosisRisk AssessmentBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID41831466
PMCPMC12989675

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.