Automated volumetric breast density measures: differential change between breasts in women with and without breast cancer.


Journal

Breast cancer research : BCR
ISSN: 1465-542X
Titre abrégé: Breast Cancer Res
Pays: England
ID NLM: 100927353

Informations de publication

Date de publication:
28 10 2019
Historique:
received: 22 04 2019
accepted: 13 09 2019
entrez: 30 10 2019
pubmed: 30 10 2019
medline: 9 4 2020
Statut: epublish

Résumé

Given that breast cancer and normal dense fibroglandular tissue have similar radiographic attenuation, we examine whether automated volumetric density measures identify a differential change between breasts in women with cancer and compare to healthy controls. Eligible cases (n = 1160) had unilateral invasive breast cancer and bilateral full-field digital mammograms (FFDMs) at two time points: within 2 months and 1-5 years before diagnosis. Controls (n = 2360) were matched to cases on age and date of FFDMs. Dense volume (DV) and volumetric percent density (VPD) for each breast were assessed using Volpara™. Differences in DV and VPD between mammograms (median 3 years apart) were calculated per breast separately for cases and controls and their difference evaluated by using the Wilcoxon signed-rank test. To simulate clinical practice where cancer laterality is unknown, we examined whether the absolute difference between breasts can discriminate cases from controls using area under the ROC curve (AUC) analysis, adjusting for age, BMI, and time. Among cases, the VPD and DV between mammograms of the cancerous breast decreased to a lesser degree (- 0.26% and - 2.10 cm There is a small relative increase in volumetric density measures over time in the breast with cancer which is not found in the normal breast. However, the magnitude of this difference is small, and this measure alone does not appear to be a good discriminator between women with and without breast cancer.

Sections du résumé

BACKGROUND
Given that breast cancer and normal dense fibroglandular tissue have similar radiographic attenuation, we examine whether automated volumetric density measures identify a differential change between breasts in women with cancer and compare to healthy controls.
METHODS
Eligible cases (n = 1160) had unilateral invasive breast cancer and bilateral full-field digital mammograms (FFDMs) at two time points: within 2 months and 1-5 years before diagnosis. Controls (n = 2360) were matched to cases on age and date of FFDMs. Dense volume (DV) and volumetric percent density (VPD) for each breast were assessed using Volpara™. Differences in DV and VPD between mammograms (median 3 years apart) were calculated per breast separately for cases and controls and their difference evaluated by using the Wilcoxon signed-rank test. To simulate clinical practice where cancer laterality is unknown, we examined whether the absolute difference between breasts can discriminate cases from controls using area under the ROC curve (AUC) analysis, adjusting for age, BMI, and time.
RESULTS
Among cases, the VPD and DV between mammograms of the cancerous breast decreased to a lesser degree (- 0.26% and - 2.10 cm
CONCLUSION
There is a small relative increase in volumetric density measures over time in the breast with cancer which is not found in the normal breast. However, the magnitude of this difference is small, and this measure alone does not appear to be a good discriminator between women with and without breast cancer.

Identifiants

pubmed: 31660981
doi: 10.1186/s13058-019-1198-9
pii: 10.1186/s13058-019-1198-9
pmc: PMC6819393
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

118

Subventions

Organisme : NCI NIH HHS
ID : P01 CA154292
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA177150
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA207084
Pays : United States

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Auteurs

Kathleen R Brandt (KR)

Department of Radiology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA. brandt.kathy@mayo.edu.

Christopher G Scott (CG)

Department of Health Sciences Research, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Diana L Miglioretti (DL)

Kaiser Permanente Washington Health Research Institute, 1730 Minor Avenue, Seattle, WA, 98101, USA.

Matthew R Jensen (MR)

Department of Health Sciences Research, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Amir P Mahmoudzadeh (AP)

Department of Radiology and Biomedical Imaging, University of California, 505 Parnassus Avenue, San Francisco, CA, 94143, USA.

Carrie Hruska (C)

Department of Radiology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Lin Ma (L)

Division of Research, Kaiser Permanente, 2000 Broadway, Oakland, CA, 94612, USA.

Fang Fang Wu (FF)

Department of Health Sciences Research, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Steven R Cummings (SR)

California Pacific Medical Center Research Institute, 475 Brannan Street #220, San Francisco, CA, 94107, USA.

Aaron D Norman (AD)

Department of Health Sciences Research, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Natalie J Engmann (NJ)

Department of Epidemiology and Biostatistics, University of California, 550 16th Street, Second Floor, San Francisco, CA, 94158, USA.

John A Shepherd (JA)

University of Hawaii Cancer Center, 701 Ilalo Street, Honolulu, HI, 96813, USA.

Stacey J Winham (SJ)

Department of Health Sciences Research, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Karla Kerlikowske (K)

Department of Epidemiology and Biostatistics, University of California, 550 16th Street, Second Floor, San Francisco, CA, 94158, USA.

Celine M Vachon (CM)

Department of Health Sciences Research, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

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Classifications MeSH