Evidence map›Paper›PMID 26514439›Full record

ArticleAcademic radiology2016

Comparing Mammography Abnormality Features to Genetic Variants in the Prediction of Breast Cancer in Women Recommended for Breast Biopsy.

Elizabeth S Burnside, Jie Liu, Yirong Wu, Adedayo A Onitilo, Catherine A McCarty, C David Page, Peggy L Peissig, Amy Trentham-Dietz, Terrie Kitchner, Jun Fan and 1 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Academic radiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Prediction of Breast Cancer using Machine Learning Approaches.Journal of biomedical physics & engineering · 2022
    Article
  2. Review
  3. Quantifying predictive capability of electronic health records for the most harmful breast cancer.Proceedings of SPIE--the International Society for Optical Engineering · 2018
    Article
  4. Utility of Genetic Testing in Addition to Mammography for Determining Risk of Breast Cancer Depends on Patient Age.AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science · 2018
    Article
  5. Article
  6. Structure-Leveraged Methods in Breast Cancer Risk Prediction.Journal of machine learning research : JMLR · 2016
    Article
  7. Discriminatory power of common genetic variants in personalized breast cancer diagnosis.Proceedings of SPIE--the International Society for Optical Engineering · 2016
    Article
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

11 authors at 3 institutions in 1 country.

Elizabeth S BurnsideDepartment of Radiology, University of Wisconsin School of Medicine and Public Health, E3/311 Clinical Science Center, 600 Highland Ave., Madison, WI 53792-3252; Department of Biostatistics and Medical Informatics, University of Wisconsin, Madison, Wisconsin. Electronic address: eburnside@uwhealth.org.
Jie LiuDepartment of Biostatistics and Medical Informatics, University of Wisconsin, Madison, Wisconsin.
Yirong WuDepartment of Radiology, University of Wisconsin School of Medicine and Public Health, E3/311 Clinical Science Center, 600 Highland Ave., Madison, WI 53792-3252.
Adedayo A OnitiloMarshfield Clinic Research Foundation, Marshfield, Wisconsin; Department of Hematology/Oncology, Marshfield Clinic Weston Center, Weston, Wisconsin.
Catherine A McCartyEssentia Institute of Rural Health, Duluth, Minnesota.
C David PageDepartment of Biostatistics and Medical Informatics, University of Wisconsin, Madison, Wisconsin.
Peggy L PeissigMarshfield Clinic Research Foundation, Marshfield, Wisconsin.
Amy Trentham-DietzDepartment of Population Health Sciences, University of Wisconsin, Madison, Wisconsin.
Terrie KitchnerMarshfield Clinic Research Foundation, Marshfield, Wisconsin.
Jun FanDepartment of Statistics, University of Wisconsin, Madison, Wisconsin; Morgridge Institute for Research, Madison, Wisconsin.
Ming YuanDepartment of Statistics, University of Wisconsin, Madison, Wisconsin; Morgridge Institute for Research, Madison, Wisconsin.
University of Wisconsin–Madison · USMarshfield Clinic · USEssentia Health · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Christian Capitini · 1985 to 2026
$142.6M
Institutional Clinical and Translational Science AwardUL1TR000427 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$32.2M
TrainingU54AI117924 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI CRAVEN, MARK W. · 2014 to 2018
$11.3M
Machine Learning for Identifying Adverse Drug EventsR01GM097618 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI CALDWELL, MICHAEL DEFOIX, HANSEN, RICHARD A. · 2011 to 2018
$3.8M
Genome-Wide Study of Cataract and Low HDL in the Personalized Medicine Research PU01HG004608 · NHGRI · MARSHFIELD CLINIC RESEARCH FOUNDATION · PI MCCARTY, CATHERINE ANNE · 2007 to 2010
$3.3M
Secure Sharing of Clinical History & Genetic Data: Empowering Predictive Pers. MeR01LM011028 · NLM · UNIVERSITY OF WISCONSIN-MADISON · PI PAGE, CHARLES DAVID · 2011 to 2014
$2.2M
Breast Cancer GWAS: Function and Environmental InteractionsR01ES017400 · NIEHS · UNIVERSITY OF WISCONSIN-MADISON · PI GOULD, MICHAEL N, NEWTON, MICHAEL A · 2009 to 2013
$2.1M
Machine Learning for Improved Mammography ScreeningR01CA127379 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI BURNSIDE, ELIZABETH S · 2007 to 2010
$1.4M
Mentoring And Research In Patient-Oriented Breast Cancer DiagnosisK24CA194251 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI BURNSIDE, ELIZABETH S · 2015 to 2019
$963k
NCATS NIH HHS UL1 TR000427NCI NIH HHS K24 CA194251NCI NIH HHS P30 CA014520NCI NIH HHS R01 CA127379NHGRI NIH HHS U01 HG004608NIAID NIH HHS U54 AI117924NIEHS NIH HHS R01 ES017400NIGMS NIH HHS R01 GM097618NLM NIH HHS R01 LM011028
6 · The paper itself

Abstract

RATIONALE AND

objectivesThe discovery of germline genetic variants associated with breast cancer has engendered interest in risk stratification for improved, targeted detection and diagnosis. However, there has yet to be a comparison of the predictive ability of these genetic variants with mammography abnormality descriptors. MATERIALS AND

methodsOur institutional review board-approved, Health Insurance Portability and Accountability Act-compliant study utilized a personalized medicine registry in which participants consented to provide a DNA sample and to participate in longitudinal follow-up. In our retrospective, age-matched, case-controlled study of 373 cases and 395 controls who underwent breast biopsy, we collected risk factors selected a priori based on the literature, including demographic variables based on the Gail model, common germline genetic variants, and diagnostic mammography findings according to Breast Imaging Reporting and Data System (BI-RADS). We developed predictive models using logistic regression to determine the predictive ability of (1) demographic variables, (2) 10 selected genetic variants, or (3) mammography BI-RADS features. We evaluated each model in turn by calculating a risk score for each patient using 10-fold cross-validation, used this risk estimate to construct Receiver Operator Characteristic Curve (ROC) curves, and compared the area under the ROC curve (AUC) of each using the DeLong method.

resultsThe performance of the regression model using demographic risk factors was not statistically different from the model using genetic variants (P = 0.9). The model using mammography features (AUC = 0.689) was superior to both the demographic model (AUC = .598; P < 0.001) and the genetic model (AUC = .601; P < 0.001).

conclusionsBI-RADS features exceeded the ability of demographic and 10 selected germline genetic variants to predict breast cancer in women recommended for biopsy.

Indexed as

AdultAgedAged, 80 and overBiopsyBreastBreast NeoplasmsEpidemiologic MethodsFemaleGenes, BRCA1Genes, BRCA2HumansMammographyMiddle AgedPolymorphism, Single NucleotideUnited StatesYoung AdultBI-RADSGenetic variantsMammographyPredictive valueRisk estimation

Identifiers

PMID26514439
PMCPMC4684977
OpenAlexW1880589229

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.