Evidence map›Paper›PMID 41885411›Full record

ArticleJournal of the National Cancer Institute2026

Performance of clinical breast cancer risk prediction models vs a mammography-based artificial intelligence risk model.

Medha Kaul, Christopher G Scott, Alena Wadzinske, Imon Banerjee, Dan Hursh, Aaron Norman, Fang-Fang Wu, Ramon Correa-Medero, Fergus Couch, Sandhya Pruthi and 6 more

Abstract readComparative Study
In one paragraph

Article in Journal of the National Cancer Institute, 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.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Medha KaulDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, United States.ORCID 0009-0005-6040-217X
Christopher G ScottDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, United States.ORCID 0000-0003-1340-0647
Alena WadzinskeDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, United States.ORCID 0009-0000-7641-3096
Imon BanerjeeDepartment of Radiology, Mayo Clinic, Phoenix, AZ, United States.ORCID 0000-0002-3327-8004
Dan HurshDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, United States.
Aaron NormanDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, United States.ORCID 0000-0002-4208-2708
Fang-Fang WuDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, United States.
Ramon Correa-MederoDepartment of Radiology, Mayo Clinic, Phoenix, AZ, United States.ORCID 0000-0003-2247-7777
Fergus CouchDivision of Experimental Pathology and Laboratory Medicine, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, United States.ORCID 0000-0001-9417-9985
Sandhya PruthiDivision of General Internal Medicine, Department of Internal Medicine, Mayo Clinic, Rochester, MN, United States.ORCID 0000-0002-2235-4542
Despina KontosDepartment of Radiology, Columbia University Irving Medical Center, New York City, NY, United States.ORCID 0000-0001-9031-5126
Anne Marie McCarthyDepartments of Biostatistics and Epidemiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, United States.ORCID 0000-0002-3068-2669
Janet OlsonDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, United States.
Stacey WinhamDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, United States.ORCID 0000-0002-8492-9102
Karla KerlikowskeDepartments of Medicine and Epidemiology and Biostatistics, University of California San Francisco, San Francisco, CA, United States.ORCID 0000-0001-8793-8779
Celine M VachonDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, United States.ORCID 0000-0002-1962-9322

Funding

Risk-based Imaging Strategies to Improve Breast Cancer Surveillance OutcomesP01CA154292 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Diana L Miglioretti · 2011 to 2026
$52.9M
Evaluation of novel tomosynthesis density measures in breast cancer risk predictionR01CA275074 · NCI · MAYO CLINIC ROCHESTER · PI KARLA M KERLIKOWSKE, Despina Kontos · 2023 to 2026
$2.7M
Department of Defense HT9425-23-1 to 0234Hoveida Family FoundationMayo Clinic Cancer CenterNCI NIH HHS P01 CA154292NCI NIH HHS R01 CA275074NIH HHS R01 CA275074
6 · The paper itself

Abstract

backgroundArtificial intelligence (AI)-based, mammography breast cancer risk prediction models show improved discriminatory accuracy relative to clinical risk models. However, data on their calibration are limited. This study compared model performance of 3 clinical breast cancer risk models: Gail, Tyrer-Cuzick v8, and Breast Cancer Surveillance Consortium v3 with the MIRAI AI-risk model.

methodsDigital mammograms were ascertained from a screening mammography cohort of 12 308 women within the Mayo Clinic Biobank with 250 incident breast cancers (176 invasive) within 5 years. We predicted 5-year breast cancer risk, estimated discriminatory accuracy (C-index), and calibration (observed-to-expected ratio) of both overall and invasive breast cancer and compared estimates using bootstrapping approaches.

resultsMIRAI demonstrated similar or improved discriminatory accuracy of overall breast cancer (C-index = 0.71, 95% confidence interval [CI] = 0.68 to 0.74) and invasive breast cancer (C-index = 0.71, 95% CI = 0.67 to 0.75) compared with clinical models (overall breast cancer: C-index = 0.59-0.68; invasive breast cancer: C-index = 0.60-0.68). MIRAI's calibration for risk of overall breast cancer (observed-to-expected ratio = 0.96, 95% CI = 0.85 to 1.08) was improved compared with Gail (observed-to-expected ratio = 1.22, 95% CI = 1.07 to 1.38) and Breast Cancer Surveillance Consortium (observed-to-expected ratio = 1.38, 95% CI = 1.22 to 1.56) but similar to TC with volumetric percent density and polygenic risk score (observed-to-expected ratio = 0.99, 95% CI = 0.87 to 1.13). However, for low-risk women (approximately 50%), MIRAI overestimated risk of overall breast cancer. MIRAI also overestimated risk of invasive breast cancer across the risk spectrum (observed-to-expected ratio = 0.68, 95% CI = 0.58 to 0.78), whereas clinical models had good calibration (observed-to-expected ratio = 0.86-0.99).

conclusionMIRAI demonstrated stronger discriminatory accuracy than clinical models for 5-year overall and invasive breast cancer risk prediction but overestimated risk for both breast cancer endpoints. AI-based risk models should consider discriminatory accuracy and calibration for invasive cancer before implementation.

Indexed as

Artificial IntelligenceBreast NeoplasmsMammographyAdultAgedEarly Detection of CancerFemaleHumansMiddle AgedPrediction AlgorithmsRisk AssessmentRisk Factors

Identifiers

PMID41885411
PMCPMC13403648

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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.