Evidence map›Paper›PMID 31221197›Full record

ArticleBreast cancer research : BCR2019

Machine learning techniques for personalized breast cancer risk prediction: comparison with the BCRAT and BOADICEA models.

Chang Ming, Valeria Viassolo, Nicole Probst-Hensch, Pierre O Chappuis, Ivo D Dinov, Maria C Katapodi

Abstract read
In one paragraph

Article in Breast cancer research : BCR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 3 pooled it
–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

43 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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  10. Application of machine-learning model to optimize colonic adenoma detection in India.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Chang MingNursing Science, Faculty of Medicine, University of Basel, Bernoullistrasse 28, Room 118, 4056, Basel, Switzerland. chang.ming@unibas.ch.ORCID http://orcid.org/0000-0002-2817-3865
Valeria ViassoloOncogenetics and Cancer Prevention, Geneva University Hospitals, Geneva, Switzerland.
Nicole Probst-HenschSwiss Tropical and Public Health Institute, University of Basel, Basel, Switzerland.
Pierre O ChappuisOncogenetics and Cancer Prevention, Geneva University Hospitals, Geneva, Switzerland.
Ivo D DinovDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, USA.
Maria C KatapodiNursing Science, Faculty of Medicine, University of Basel, Bernoullistrasse 28, Room 118, 4056, Basel, Switzerland.

Funding

Pilot and Feasibility (P and F) ProgramP30DK089503 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Kanakadurga Singer · 2010 to 2026
$20.3M
TrainingU54EB020406 · NIBIB · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TOGA, ARTHUR W · 2014 to 2018
$12.5M
Michigan Alzheimer's Disease Core CenterP30AG053760 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PAULSON, HENRY L · 2016 to 2020
$10.1M
Public Outreach and Education CoreP50NS091856 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ALBIN, ROGER L · 2014 to 2019
$10.1M
PREVENTION RESEARCH CENTER OF MICHIGANU48DP001901 · DP · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZIMMERMAN, MARC A · 2009 to 2013
$5.9M
Pilot Projects CoreP20NR015331 · NINR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LARSON, JANET L. · 2014 to 2018
$1.3M
Impact of Geospatial Factors and Environmental Pollutants on Amyotrophic Lateral Sclerosis in the State of MichiganK23ES027221 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GOUTMAN, STEPHEN · 2017 to 2021
$1.0M
NCCDPHP CDC HHS U48 DP001901NIA NIH HHS P30 AG053760NIBIB NIH HHS U54 EB020406NIDDK NIH HHS P30 DK089503NIEHS NIH HHS K23 ES027221NINDS NIH HHS P50 NS091856NINR NIH HHS P20 NR015331
6 · The paper itself

Abstract

backgroundComprehensive breast cancer risk prediction models enable identifying and targeting women at high-risk, while reducing interventions in those at low-risk. Breast cancer risk prediction models used in clinical practice have low discriminatory accuracy (0.53-0.64). Machine learning (ML) offers an alternative approach to standard prediction modeling that may address current limitations and improve accuracy of those tools. The purpose of this study was to compare the discriminatory accuracy of ML-based estimates against a pair of established methods-the Breast Cancer Risk Assessment Tool (BCRAT) and Breast and Ovarian Analysis of Disease Incidence and Carrier Estimation Algorithm (BOADICEA) models.

methodsWe quantified and compared the performance of eight different ML methods to the performance of BCRAT and BOADICEA using eight simulated datasets and two retrospective samples: a random population-based sample of U.S. breast cancer patients and their cancer-free female relatives (N = 1143), and a clinical sample of Swiss breast cancer patients and cancer-free women seeking genetic evaluation and/or testing (N = 2481).

resultsPredictive accuracy (AU-ROC curve) reached 88.28% using ML-Adaptive Boosting and 88.89% using ML-random forest versus 62.40% with BCRAT for the U.S. population-based sample. Predictive accuracy reached 90.17% using ML-adaptive boosting and 89.32% using ML-Markov chain Monte Carlo generalized linear mixed model versus 59.31% with BOADICEA for the Swiss clinic-based sample.

conclusionsThere was a striking improvement in the accuracy of classification of women with and without breast cancer achieved with ML algorithms compared to the state-of-the-art model-based approaches. High-accuracy prediction techniques are important in personalized medicine because they facilitate stratification of prevention strategies and individualized clinical management.

Indexed as

Disease SusceptibilityMachine LearningModels, TheoreticalPrecision MedicineAdultAlgorithmsBig DataBreast NeoplasmsFemaleGenetic Predisposition to DiseaseHumansMiddle AgedPopulation SurveillancePrognosisRisk AssessmentROC CurveBig dataBreast cancerCancer screeningMachine learningPersonalized medicineRisk prediction

Identifiers

PMID31221197
PMCPMC6585114

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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.