Quantitative breast density analysis to predict interval and node-positive cancers in pursuit of improved screening protocols: a case–control study

Background This study investigates whether quantitative breast density (BD) serves as an imaging biomarker for more intensive breast cancer screening by predicting interval, and node-positive cancers. Methods This case–control study of 1204 women aged 47–73 includes 599 cancer cases (302 screen-dete...

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Veröffentlicht in:British journal of cancer 2021-09, Vol.125 (6), p.884-892
Hauptverfasser: Burnside, Elizabeth S., Warren, Lucy M., Myles, Jonathan, Wilkinson, Louise S., Wallis, Matthew G., Patel, Mishal, Smith, Robert A., Young, Kenneth C., Massat, Nathalie J., Duffy, Stephen W.
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container_end_page 892
container_issue 6
container_start_page 884
container_title British journal of cancer
container_volume 125
creator Burnside, Elizabeth S.
Warren, Lucy M.
Myles, Jonathan
Wilkinson, Louise S.
Wallis, Matthew G.
Patel, Mishal
Smith, Robert A.
Young, Kenneth C.
Massat, Nathalie J.
Duffy, Stephen W.
description Background This study investigates whether quantitative breast density (BD) serves as an imaging biomarker for more intensive breast cancer screening by predicting interval, and node-positive cancers. Methods This case–control study of 1204 women aged 47–73 includes 599 cancer cases (302 screen-detected, 297 interval; 239 node-positive, 360 node-negative) and 605 controls. Automated BD software calculated fibroglandular volume (FGV), volumetric breast density (VBD) and density grade (DG). A radiologist assessed BD using a visual analogue scale (VAS) from 0 to 100. Logistic regression and area under the receiver operating characteristic curves (AUC) determined whether BD could predict mode of detection (screen-detected or interval); node-negative cancers; node-positive cancers, and all cancers vs. controls. Results FGV, VBD, VAS, and DG all discriminated interval cancers (all p  
doi_str_mv 10.1038/s41416-021-01466-y
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Methods This case–control study of 1204 women aged 47–73 includes 599 cancer cases (302 screen-detected, 297 interval; 239 node-positive, 360 node-negative) and 605 controls. Automated BD software calculated fibroglandular volume (FGV), volumetric breast density (VBD) and density grade (DG). A radiologist assessed BD using a visual analogue scale (VAS) from 0 to 100. Logistic regression and area under the receiver operating characteristic curves (AUC) determined whether BD could predict mode of detection (screen-detected or interval); node-negative cancers; node-positive cancers, and all cancers vs. controls. Results FGV, VBD, VAS, and DG all discriminated interval cancers (all p  &lt; 0.01) from controls. Only FGV-quartile discriminated screen-detected cancers ( p  &lt; 0.01). Based on AUC, FGV discriminated all cancer types better than VBD or VAS. FGV showed a significantly greater discrimination of interval cancers, AUC = 0.65, than of screen-detected cancers, AUC = 0.61 ( p  &lt; 0.01) as did VBD (0.63 and 0.53, respectively, p  &lt; 0.001). Conclusion FGV, VBD, VAS and DG discriminate interval cancers from controls, reflecting some masking risk. Only FGV discriminates screen-detected cancers perhaps adding a unique component of breast cancer risk.</description><identifier>ISSN: 0007-0920</identifier><identifier>ISSN: 1532-1827</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/s41416-021-01466-y</identifier><identifier>PMID: 34168297</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/67/1347 ; 692/499 ; Aged ; Biomedical and Life Sciences ; Biomedicine ; Breast cancer ; Breast Density ; Breast Neoplasms - diagnostic imaging ; Cancer Research ; Cancer screening ; Case-Control Studies ; Drug Resistance ; Early Detection of Cancer ; Epidemiology ; Female ; Humans ; Mammography - methods ; Medical screening ; Middle Aged ; Molecular Medicine ; Oncology ; Randomized Controlled Trials as Topic ; Visual Analog Scale ; Visual discrimination</subject><ispartof>British journal of cancer, 2021-09, Vol.125 (6), p.884-892</ispartof><rights>The Author(s) 2021</rights><rights>2021. The Author(s).</rights><rights>The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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Methods This case–control study of 1204 women aged 47–73 includes 599 cancer cases (302 screen-detected, 297 interval; 239 node-positive, 360 node-negative) and 605 controls. Automated BD software calculated fibroglandular volume (FGV), volumetric breast density (VBD) and density grade (DG). A radiologist assessed BD using a visual analogue scale (VAS) from 0 to 100. Logistic regression and area under the receiver operating characteristic curves (AUC) determined whether BD could predict mode of detection (screen-detected or interval); node-negative cancers; node-positive cancers, and all cancers vs. controls. Results FGV, VBD, VAS, and DG all discriminated interval cancers (all p  &lt; 0.01) from controls. Only FGV-quartile discriminated screen-detected cancers ( p  &lt; 0.01). Based on AUC, FGV discriminated all cancer types better than VBD or VAS. FGV showed a significantly greater discrimination of interval cancers, AUC = 0.65, than of screen-detected cancers, AUC = 0.61 ( p  &lt; 0.01) as did VBD (0.63 and 0.53, respectively, p  &lt; 0.001). Conclusion FGV, VBD, VAS and DG discriminate interval cancers from controls, reflecting some masking risk. 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Methods This case–control study of 1204 women aged 47–73 includes 599 cancer cases (302 screen-detected, 297 interval; 239 node-positive, 360 node-negative) and 605 controls. Automated BD software calculated fibroglandular volume (FGV), volumetric breast density (VBD) and density grade (DG). A radiologist assessed BD using a visual analogue scale (VAS) from 0 to 100. Logistic regression and area under the receiver operating characteristic curves (AUC) determined whether BD could predict mode of detection (screen-detected or interval); node-negative cancers; node-positive cancers, and all cancers vs. controls. Results FGV, VBD, VAS, and DG all discriminated interval cancers (all p  &lt; 0.01) from controls. Only FGV-quartile discriminated screen-detected cancers ( p  &lt; 0.01). Based on AUC, FGV discriminated all cancer types better than VBD or VAS. FGV showed a significantly greater discrimination of interval cancers, AUC = 0.65, than of screen-detected cancers, AUC = 0.61 ( p  &lt; 0.01) as did VBD (0.63 and 0.53, respectively, p  &lt; 0.001). Conclusion FGV, VBD, VAS and DG discriminate interval cancers from controls, reflecting some masking risk. Only FGV discriminates screen-detected cancers perhaps adding a unique component of breast cancer risk.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>34168297</pmid><doi>10.1038/s41416-021-01466-y</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-3344-2238</orcidid><orcidid>https://orcid.org/0000-0002-1095-994X</orcidid><orcidid>https://orcid.org/0000-0003-4901-7922</orcidid><orcidid>https://orcid.org/0000-0002-6600-435X</orcidid><oa>free_for_read</oa></addata></record>
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subjects 631/67/1347
692/499
Aged
Biomedical and Life Sciences
Biomedicine
Breast cancer
Breast Density
Breast Neoplasms - diagnostic imaging
Cancer Research
Cancer screening
Case-Control Studies
Drug Resistance
Early Detection of Cancer
Epidemiology
Female
Humans
Mammography - methods
Medical screening
Middle Aged
Molecular Medicine
Oncology
Randomized Controlled Trials as Topic
Visual Analog Scale
Visual discrimination
title Quantitative breast density analysis to predict interval and node-positive cancers in pursuit of improved screening protocols: a case–control study
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