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Breast density as a determinant of interval cancer at mammographic screening
The association of breast density (% of breast volume involved by fibro-glandular densities) with the risk of interval cancer (IC) was investigated by reviewing a consecutive series of 346 cancers detected at screening (SDC) during 1996–1999 and of 90 ICs, reported as negative in the same period and...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2004
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409545/ https://www.ncbi.nlm.nih.gov/pubmed/14735182 http://dx.doi.org/10.1038/sj.bjc.6601548 |
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author | Ciatto, S Visioli, C Paci, E Zappa, M |
author_facet | Ciatto, S Visioli, C Paci, E Zappa, M |
author_sort | Ciatto, S |
collection | PubMed |
description | The association of breast density (% of breast volume involved by fibro-glandular densities) with the risk of interval cancer (IC) was investigated by reviewing a consecutive series of 346 cancers detected at screening (SDC) during 1996–1999 and of 90 ICs, reported as negative in the same period and diagnosed in the following 2 years, and comparing them to a random sample of 360 healthy controls. The probability of IC was significantly associated with breast density, whatever grouping (0/1–25/26–74/>74%; 0–25/26–60/61–74/>74%; 0–25/26–74/>74%) was considered (χ(2)=30.67–34.08, P<0.<0.01): 27.8% of all ICs were classified in the >74% density class, as compared to 7% of SDC and 5% of healthy controls. No significant association to IC was observed for Wolfe pattern (P2/Dy vs N1/P1: χ(2)=0.30, P=0.960), number of used mammographic views (single oblique vs oblique+craniocaudal: χ(2)=0.02, P=0.90) or screening round (first vs repeat: χ(2)=1.41, P=0.23). Multivariate analysis confirmed the independent association of breast density to IC, the highest risk being observed for >74% density class (OR vs 0% class=13.4, 95% CI 2.7–65.6, OR vs all other density classes=5.1, 95% CI 2.6–10.0). Age showed an independent association too, older women having a lower risk of IC (OR=0.52 95% CI 0.3–09). Breast density (>74%) resulted as being a major determinant of IC. Special screening protocols (shorter rescreening interval, routine use of ultrasonography) might be suggested for these subjects in order to improve screening sensitivity and efficacy. |
format | Text |
id | pubmed-2409545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-24095452009-09-10 Breast density as a determinant of interval cancer at mammographic screening Ciatto, S Visioli, C Paci, E Zappa, M Br J Cancer Clinical The association of breast density (% of breast volume involved by fibro-glandular densities) with the risk of interval cancer (IC) was investigated by reviewing a consecutive series of 346 cancers detected at screening (SDC) during 1996–1999 and of 90 ICs, reported as negative in the same period and diagnosed in the following 2 years, and comparing them to a random sample of 360 healthy controls. The probability of IC was significantly associated with breast density, whatever grouping (0/1–25/26–74/>74%; 0–25/26–60/61–74/>74%; 0–25/26–74/>74%) was considered (χ(2)=30.67–34.08, P<0.<0.01): 27.8% of all ICs were classified in the >74% density class, as compared to 7% of SDC and 5% of healthy controls. No significant association to IC was observed for Wolfe pattern (P2/Dy vs N1/P1: χ(2)=0.30, P=0.960), number of used mammographic views (single oblique vs oblique+craniocaudal: χ(2)=0.02, P=0.90) or screening round (first vs repeat: χ(2)=1.41, P=0.23). Multivariate analysis confirmed the independent association of breast density to IC, the highest risk being observed for >74% density class (OR vs 0% class=13.4, 95% CI 2.7–65.6, OR vs all other density classes=5.1, 95% CI 2.6–10.0). Age showed an independent association too, older women having a lower risk of IC (OR=0.52 95% CI 0.3–09). Breast density (>74%) resulted as being a major determinant of IC. Special screening protocols (shorter rescreening interval, routine use of ultrasonography) might be suggested for these subjects in order to improve screening sensitivity and efficacy. Nature Publishing Group 2004-01-26 2004-01-20 /pmc/articles/PMC2409545/ /pubmed/14735182 http://dx.doi.org/10.1038/sj.bjc.6601548 Text en Copyright © 2004 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Ciatto, S Visioli, C Paci, E Zappa, M Breast density as a determinant of interval cancer at mammographic screening |
title | Breast density as a determinant of interval cancer at mammographic screening |
title_full | Breast density as a determinant of interval cancer at mammographic screening |
title_fullStr | Breast density as a determinant of interval cancer at mammographic screening |
title_full_unstemmed | Breast density as a determinant of interval cancer at mammographic screening |
title_short | Breast density as a determinant of interval cancer at mammographic screening |
title_sort | breast density as a determinant of interval cancer at mammographic screening |
topic | Clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409545/ https://www.ncbi.nlm.nih.gov/pubmed/14735182 http://dx.doi.org/10.1038/sj.bjc.6601548 |
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