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A clinical model for identifying the short-term risk of breast cancer
BACKGROUND: Most mammography screening programs are not individualized. To efficiently screen for breast cancer, the individual risk of the disease should be determined. We describe a model that could be used at most mammography screening units without adding substantial cost. METHODS: The study was...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348894/ https://www.ncbi.nlm.nih.gov/pubmed/28288659 http://dx.doi.org/10.1186/s13058-017-0820-y |
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author | Eriksson, Mikael Czene, Kamila Pawitan, Yudi Leifland, Karin Darabi, Hatef Hall, Per |
author_facet | Eriksson, Mikael Czene, Kamila Pawitan, Yudi Leifland, Karin Darabi, Hatef Hall, Per |
author_sort | Eriksson, Mikael |
collection | PubMed |
description | BACKGROUND: Most mammography screening programs are not individualized. To efficiently screen for breast cancer, the individual risk of the disease should be determined. We describe a model that could be used at most mammography screening units without adding substantial cost. METHODS: The study was based on the Karma cohort, which included 70,877 participants. Mammograms were collected up to 3 years following the baseline mammogram. A prediction protocol was developed using mammographic density, computer-aided detection of microcalcifications and masses, use of hormone replacement therapy (HRT), family history of breast cancer, menopausal status, age, and body mass index. Relative risks were calculated using conditional logistic regression. Absolute risks were calculated using the iCARE protocol. RESULTS: Comparing women at highest and lowest mammographic density yielded a fivefold higher risk of breast cancer for women at highest density. When adding microcalcifications and masses to the model, high-risk women had a nearly ninefold higher risk of breast cancer than those at lowest risk. In the full model, taking HRT use, family history of breast cancer, and menopausal status into consideration, the AUC reached 0.71. CONCLUSIONS: Measures of mammographic features and information on HRT use, family history of breast cancer, and menopausal status enabled early identification of women within the mammography screening program at such a high risk of breast cancer that additional examinations are warranted. In contrast, women at low risk could probably be screened less intensively. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-017-0820-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5348894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53488942017-03-14 A clinical model for identifying the short-term risk of breast cancer Eriksson, Mikael Czene, Kamila Pawitan, Yudi Leifland, Karin Darabi, Hatef Hall, Per Breast Cancer Res Research Article BACKGROUND: Most mammography screening programs are not individualized. To efficiently screen for breast cancer, the individual risk of the disease should be determined. We describe a model that could be used at most mammography screening units without adding substantial cost. METHODS: The study was based on the Karma cohort, which included 70,877 participants. Mammograms were collected up to 3 years following the baseline mammogram. A prediction protocol was developed using mammographic density, computer-aided detection of microcalcifications and masses, use of hormone replacement therapy (HRT), family history of breast cancer, menopausal status, age, and body mass index. Relative risks were calculated using conditional logistic regression. Absolute risks were calculated using the iCARE protocol. RESULTS: Comparing women at highest and lowest mammographic density yielded a fivefold higher risk of breast cancer for women at highest density. When adding microcalcifications and masses to the model, high-risk women had a nearly ninefold higher risk of breast cancer than those at lowest risk. In the full model, taking HRT use, family history of breast cancer, and menopausal status into consideration, the AUC reached 0.71. CONCLUSIONS: Measures of mammographic features and information on HRT use, family history of breast cancer, and menopausal status enabled early identification of women within the mammography screening program at such a high risk of breast cancer that additional examinations are warranted. In contrast, women at low risk could probably be screened less intensively. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13058-017-0820-y) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-14 2017 /pmc/articles/PMC5348894/ /pubmed/28288659 http://dx.doi.org/10.1186/s13058-017-0820-y Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Eriksson, Mikael Czene, Kamila Pawitan, Yudi Leifland, Karin Darabi, Hatef Hall, Per A clinical model for identifying the short-term risk of breast cancer |
title | A clinical model for identifying the short-term risk of breast cancer |
title_full | A clinical model for identifying the short-term risk of breast cancer |
title_fullStr | A clinical model for identifying the short-term risk of breast cancer |
title_full_unstemmed | A clinical model for identifying the short-term risk of breast cancer |
title_short | A clinical model for identifying the short-term risk of breast cancer |
title_sort | clinical model for identifying the short-term risk of breast cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348894/ https://www.ncbi.nlm.nih.gov/pubmed/28288659 http://dx.doi.org/10.1186/s13058-017-0820-y |
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