Evidence map›Paper›PMID 37544983›Full record

ArticleBreast cancer research : BCR2023

Examination of fully automated mammographic density measures using LIBRA and breast cancer risk in a cohort of 21,000 non-Hispanic white women.

Laurel A Habel, Stacey E Alexeeff, Ninah Achacoso, Vignesh A Arasu, Aimilia Gastounioti, Lawrence Gerstley, Robert J Klein, Rhea Y Liang, Jafi A Lipson, Walter Mankowski and 13 more

Abstract read
In one paragraph

Article in Breast cancer research : BCR, 2023. 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
–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

7 citing papers in PubMed.

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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

23 authors.

Laurel A HabelDivision of Research, Kaiser Permanente Northern California, CA, Oakland, USA. laurel.habel@kp.org.
Stacey E AlexeeffDivision of Research, Kaiser Permanente Northern California, CA, Oakland, USA.
Ninah AchacosoDivision of Research, Kaiser Permanente Northern California, CA, Oakland, USA.
Vignesh A ArasuDivision of Research, Kaiser Permanente Northern California, CA, Oakland, USA.
Aimilia GastouniotiMallinckrodt Institute of Radiology, Washington University School of Medicine, Saint Louis, MO, USA.
Lawrence GerstleyDivision of Research, Kaiser Permanente Northern California, CA, Oakland, USA.
Robert J KleinDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Rhea Y LiangDepartment of Radiology, Stanford University School of Medicine, Stanford, CA, USA.
Jafi A LipsonDepartment of Radiology, Stanford University School of Medicine, Stanford, CA, USA.
Walter MankowskiDepartment of Radiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Laurie R MargoliesDepartment of Diagnostic, Molecular and Interventional Radiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Joseph H RothsteinDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Daniel L RubinDepartment of Radiology, Stanford University School of Medicine, Stanford, CA, USA.
Li ShenDepartment of Artificial Intelligence and Human Health, Icahn School of Medicine at Mount Sinai, NY, New York, USA.
Adriana SistigDepartment of Artificial Intelligence and Human Health, Icahn School of Medicine at Mount Sinai, NY, New York, USA.
Xiaoyu SongTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Marvella A VillaseñorDivision of Research, Kaiser Permanente Northern California, CA, Oakland, USA.
Mark WestleyDivision of Research, Kaiser Permanente Northern California, CA, Oakland, USA.
Alice S WhittemoreDepartment of Biomedical Data Science, Stanford University School of Medicine, Stanford, CA, USA.
Martin J YaffeSunnybrook Research Institute and Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
Pei WangDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Despina KontosDepartment of Radiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Weiva SiehDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Funding

A Resource for Genetic Epidemiology Research in Adult Health and AgingRC2AG036607 · NIA · KAISER FOUNDATION RESEARCH INSTITUTE · PI RISCH, NEIL J., SCHAEFER, CATHERINE ANN · 2009 to 2010
$24.8M
Radiomic and genomic predictors of breast cancer riskR01CA264987 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Vignesh A Arasu, Li Shen · 2021 to 2026
$3.5M
Genome-Wide Association Study of Mammographic DensityR01CA166827 · NCI · STANFORD UNIVERSITY · PI HABEL, LAUREL A, SIEH, WEIVA · 2012 to 2016
$2.3M
Mammographic Density & Prognosis among Breast Cancer Intrinsic SubtypesR01CA168893 · NCI · KAISER FOUNDATION RESEARCH INSTITUTE · PI HABEL, LAUREL A · 2012 to 2015
$2.1M
Genomic and Transcriptomic Analysis of Mammographic DensityR01CA237541 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HABEL, LAUREL A, SIEH, WEIVA · 2020 to 2023
$2.0M
NCI NIH HHS R01 CA166827NCI NIH HHS R01 CA168893NCI NIH HHS R01 CA237541NCI NIH HHS R01 CA264987NIA NIH HHS RC2 AG036607
6 · The paper itself

Abstract

backgroundBreast density is strongly associated with breast cancer risk. Fully automated quantitative density assessment methods have recently been developed that could facilitate large-scale studies, although data on associations with long-term breast cancer risk are limited. We examined LIBRA assessments and breast cancer risk and compared results to prior assessments using Cumulus, an established computer-assisted method requiring manual thresholding.

methodsWe conducted a cohort study among 21,150 non-Hispanic white female participants of the Research Program in Genes, Environment and Health of Kaiser Permanente Northern California who were 40-74 years at enrollment, followed for up to 10 years, and had archived processed screening mammograms acquired on Hologic or General Electric full-field digital mammography (FFDM) machines and prior Cumulus density assessments available for analysis. Dense area (DA), non-dense area (NDA), and percent density (PD) were assessed using LIBRA software. Cox regression was used to estimate hazard ratios (HRs) for breast cancer associated with DA, NDA and PD modeled continuously in standard deviation (SD) increments, adjusting for age, mammogram year, body mass index, parity, first-degree family history of breast cancer, and menopausal hormone use. We also examined differences by machine type and breast view.

resultsThe adjusted HRs for breast cancer associated with each SD increment of DA, NDA and PD were 1.36 (95% confidence interval, 1.18-1.57), 0.85 (0.77-0.93) and 1.44 (1.26-1.66) for LIBRA and 1.44 (1.33-1.55), 0.81 (0.74-0.89) and 1.54 (1.34-1.77) for Cumulus, respectively. LIBRA results were generally similar by machine type and breast view, although associations were strongest for Hologic machines and mediolateral oblique views. Results were also similar during the first 2 years, 2-5 years and 5-10 years after the baseline mammogram.

conclusionAssociations with breast cancer risk were generally similar for LIBRA and Cumulus density measures and were sustained for up to 10 years. These findings support the suitability of fully automated LIBRA assessments on processed FFDM images for large-scale research on breast density and cancer risk.

Indexed as

Breast NeoplasmsBreastBreast DensityCase-Control StudiesCohort StudiesFemaleHumansMammographyRisk FactorsWhiteBreast cancerEpidemiologyMammographic densityMammographyRisk factors

Identifiers

PMID37544983
PMCPMC10405373

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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.