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Quantitative breast density analysis to predict interval and node-positive cancers in pursuit of improved screening protocols: a case-control study.
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.
Afiliação
  • Burnside ES; Department of Radiology, University of Wisconsin-Madison School of Medicine and Public Health, E3/311 Clinical Science Center, Madison, WI, USA. eburnside@wisc.edu.
  • Warren LM; National Co-ordinating Centre for the Physics of Mammography (NCCPM), Medical Physics Department, Royal Surrey County Hospital, Guildford, UK.
  • Myles J; Centre for Cancer Prevention, Queen Mary University of London, Wolfson Institute of Preventive Medicine, London, UK.
  • Wilkinson LS; Oxford Breast Imaging Centre, Churchill Hospital, Oxford, UK.
  • Wallis MG; Cambridge Breast Unit and NIHR Cambridge Biomedical Research Centre, Cambridge University Hospitals NHS Trust, Cambridge, UK.
  • Patel M; Scientific Computing, Medical Physics Department, Royal Surrey County Hospital, Guildford, UK.
  • Smith RA; American Cancer Society, Atlanta, GA, USA.
  • Young KC; National Co-ordinating Centre for the Physics of Mammography (NCCPM), Medical Physics Department, Royal Surrey County Hospital, Guildford, UK.
  • Massat NJ; Centre for Cancer Prevention, Queen Mary University of London, Wolfson Institute of Preventive Medicine, London, UK.
  • Duffy SW; Centre for Cancer Prevention, Queen Mary University of London, Wolfson Institute of Preventive Medicine, London, UK.
Br J Cancer ; 125(6): 884-892, 2021 09.
Article em En | MEDLINE | ID: mdl-34168297
ABSTRACT

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 < 0.01) from controls. Only FGV-quartile discriminated screen-detected cancers (p < 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 < 0.01) as did VBD (0.63 and 0.53, respectively, p < 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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Mamografia / Densidade da Mama Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Aged / Female / Humans / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Mamografia / Densidade da Mama Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Aged / Female / Humans / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article