Evidence map›Paper›PMID 42132486›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2026

Performance of Statistical and Machine Learning Risk Prediction Models for Advanced Breast Cancer.

Shuai Chen, Karla Kerlikowske, Yu-Ru Su, Rebecca A Hubbard, Charlotte C Gard, Jeffrey A Tice, Brian L Sprague, Thomas P Ahern, Diana L Miglioretti

Abstract read
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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

9 authors.

Shuai ChenDepartment of Public Health Sciences, University of California, Davis, California.ORCID 0000-0002-4016-8217
Karla KerlikowskeDepartment of Medicine, University of California, San Francisco, California.ORCID 0000-0001-8793-8779
Yu-Ru SuKaiser Permanente Washington Health Research Institute , Kaiser Permanente Washington, Seattle, Washington.ORCID 0000-0001-6150-960X
Rebecca A HubbardDepartment of Biostatistics, Brown University, Providence, Rhode Island.ORCID 0000-0003-0879-0994
Charlotte C GardDepartment of Economics, Applied Statistics, and International Business, New Mexico State University, Las Cruces, New Mexico.ORCID 0000-0001-7201-4450
Jeffrey A TiceDivision of General Internal Medicine, Department of Medicine, University of California, San Francisco, San Francisco, California.ORCID 0000-0002-9857-2028
Brian L SpragueDepartment of Surgery, University of Vermont, Burlington, Vermont.ORCID 0000-0001-7948-8317
Thomas P AhernDepartment of Surgery, University of Vermont, Burlington, Vermont.ORCID 0000-0003-0440-8727
Diana L MigliorettiDepartment of Public Health Sciences, University of California, Davis, California.ORCID 0000-0002-5547-1833

Funding

Staff InvestigatorsP30CA093373 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI Laura Marcu · 2002 to 2026
$84.9M
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
Understanding Factors Influencing COVID-19 Testing and Vaccination in Immigrant Low-income and Homeless Populations and Testing Targeted InterventionsU54GM115516 · NIGMS · MAINEHEALTH · PI Brenda Morissette Joly · 2017 to 2026
$51.6M
Identifying effective risk-based supplemental ultrasound screening strategies for women with dense breastsR01CA248068 · NCI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI Diana L Miglioretti, Brian L Sprague · 2020 to 2026
$5.1M
Using gene expression to identify patients at high risk for late breast cancer recurrenceR01CA286069 · NCI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI Thomas Patrick Ahern · 2024 to 2026
$1.7M
National Cancer Institute (NCI) P01CA154292National Cancer Institute (NCI) R01CA248068National Cancer Institute (NCI) R01CA286069National Institute of General Medical Sciences (NIGMS) U54GM115516NCI NIH HHS P01 CA154292NCI NIH HHS P30 CA093373NCI NIH HHS R01 CA248068NCI NIH HHS R01 CA286069NIGMS NIH HHS U54 GM115516
6 · The paper itself

Abstract

backgroundMachine learning enables complex risk prediction models, but comparative performance with statistical approaches remains context-dependent. We compared statistical and machine learning models for predicting advanced breast cancer risk.

methodsUsing data from 968,178 women (40-74 years) undergoing 2,796,459 annual or 812,126 biennial screening mammograms (2005-2019) in the Breast Cancer Surveillance Consortium, we cross-validated models predicting advanced breast cancer within 12 months (annual) or 24 months (biennial) following screening. Models included conventional logistic regression, regularized regressions [least absolute shrinkage and selection operator (LASSO), elastic net], and machine learning methods (random forests, gradient boosting), considering a modest number of clinical and demographic predictors. Performance was assessed using calibration and area under the receiver operating characteristic curve (AUC).

resultsDiscrimination was similar across models (AUC 0.677-0.690). Calibration differences were more pronounced. Regularized regressions achieved the most favorable calibration overall and across racial and ethnic groups, with an AUC of 0.689 [95% confidence interval (CI), 0.676-0.701]. Gradient boosting showed a comparable AUC but suboptimal calibration (calibration slope 1.12; 95% CI, 1.04-1.20). Conventional logistic regression had a slightly lower AUC (0.683; 95% CI, 0.671-0.696) and a calibration slope of 0.90 (95% CI, 0.83-0.96). Regression-based approaches were generally well calibrated across racial and ethnic groups (expected-to-observed event ratio 0.96-1.03; calibration intercept -0.03 to 0.04), with some subgroup deviations in calibration slopes (<1).

conclusionsFor predicting advanced breast cancers, regularized regression demonstrated similar discrimination and generally more favorable calibration than other approaches. IMPACT: In settings with rare outcomes and low-dimensional features, regularized regression may offer a practical balance between performance and interpretability.

Indexed as

Breast NeoplasmsEarly Detection of CancerMachine LearningAdultAgedBoosting Machine Learning AlgorithmsClassification AlgorithmsFemaleHumansMammographyMiddle AgedPrediction AlgorithmsPredictive Learning ModelsRandom ForestRisk AssessmentRisk Factors

Identifiers

PMID42132486
PMCPMC13286512

What OpenQuestion holds

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Registered trials

None linked

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.