Evidence map›Paper›PMID 41895875›Full record

ArticleESMO open2026

A machine learning assay to predict disease recurrence in hormone receptor-positive breast cancer.

L Boscolo Bielo, D Trapani, P Razavi, S Chandarlapaty, Y Zhan, G Curigliano

Abstract read
In one paragraph

Article in ESMO open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

L Boscolo BieloEarly Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, Milan, Italy; Department of Oncology and Hemato-Oncology, University of Milano, Milan, Italy; Breast Medicine Service, Department of Medicine, MSK, New York, USA. Electronic address: luca.boscolobielo@ieo.it.
D TrapaniEarly Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, Milan, Italy; Department of Oncology and Hemato-Oncology, University of Milano, Milan, Italy.
P RazaviBreast Medicine Service, Department of Medicine, MSK, New York, USA; Weill-Cornell Medical College, New York, USA.
S ChandarlapatyBreast Medicine Service, Department of Medicine, MSK, New York, USA; Weill-Cornell Medical College, New York, USA; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, USA.
Y ZhanDepartment of Oncology and Hemato-Oncology, University of Milano, Milan, Italy; Diagnostica Molecolare Avanzata, Department of Experimental Oncology, European Institute of Oncology IRCCS, Milan, Italy. Electronic address: yinxiu.zhan@ieo.it.
G CuriglianoEarly Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, Milan, Italy; Department of Oncology and Hemato-Oncology, University of Milano, Milan, Italy. Electronic address: giuseppe.curigliano@ieo.it.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundHormone receptor (HR)-positive, human epidermal growth factor 2 (HER2)-negative breast cancer associates with a sustained risk of relapse over time. Current multigene assays offer limited validity to identify clinically low-risk tumors at high risk of recurrence, which is particularly relevant in the context of novel adjuvant therapies. In this study, we developed and validated ER-Predict, a machine learning assay leveraging a 14-gene expression signature to classify early stage HR-positive/HER2-negative breast cancer according to the risk of relapse. MATERIALS AND

methodsER-Predict was developed on a cohort of 1413 HR-positive/HER2-negative early breast cancer cases. External validation was carried out across eight publicly available cohorts (n = 1118). Comparative benchmarking was conducted against reproduced prognostic signatures, and particularly, EndoPredict and Oncotype DX. Functional annotation and drug response analysis were carried out using gene expression and pharmacogenomic data from publicly available breast cancer cell lines.

resultsER-Predict identified high-risk patients with significantly reduced distant metastasis-free survival in the external validation cohort (hazard ratio 2.03, 95% confidence interval 1.57-2.63, P < 0.0001). The assay demonstrated independent prognostic value beyond traditional clinicopathological factors, including tumor grade, tumor size, and nodal status, and consistently outperformed recomputed multigene panels. ER-Predict showed specificity toward luminal-like transcriptomic programs, revealing activation of key cell-cycle regulators governing endocrine resistance among high-risk tumors that had retained expression of retinoblastoma-1, suggesting potential actionability by means of cell-cycle inhibitors.

conclusionsER-Predict represents a robust assay with potential utility in early stage HR-positive/HER2-negative breast cancer. Its consistent ability to identify high-risk patients supports further investigation as a decision-support tool to guide treatment intensification in clinically low-risk HR-positive/HER2-negative disease.

Indexed as

Breast NeoplasmsMachine LearningNeoplasm Recurrence, LocalReceptors, EstrogenErb-b2 Receptor Tyrosine KinasesFemaleHumansPrediction AlgorithmsPredictive Learning ModelsPrognosisERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesReceptors, Estrogenartificial intelligencebreast cancermachine learningrecurrence prediction

Identifiers

PMID41895875
PMCPMC13040913

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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.