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Columnar cell lesions and subsequent breast cancer risk: a nested case-control study

INTRODUCTION: Histologic and genetic evidence suggests that at least some columnar cell lesions (CCL) of the breast represent precursor lesions in the low-grade breast neoplasia pathway. However, the risk of subsequent breast cancer associated with the presence of CCL in a benign breast biopsy is po...

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Autores principales: Aroner, Sarah A, Collins, Laura C, Schnitt, Stuart J, Connolly, James L, Colditz, Graham A, Tamimi, Rulla M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949654/
https://www.ncbi.nlm.nih.gov/pubmed/20691043
http://dx.doi.org/10.1186/bcr2624
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author Aroner, Sarah A
Collins, Laura C
Schnitt, Stuart J
Connolly, James L
Colditz, Graham A
Tamimi, Rulla M
author_facet Aroner, Sarah A
Collins, Laura C
Schnitt, Stuart J
Connolly, James L
Colditz, Graham A
Tamimi, Rulla M
author_sort Aroner, Sarah A
collection PubMed
description INTRODUCTION: Histologic and genetic evidence suggests that at least some columnar cell lesions (CCL) of the breast represent precursor lesions in the low-grade breast neoplasia pathway. However, the risk of subsequent breast cancer associated with the presence of CCL in a benign breast biopsy is poorly understood. METHODS: The authors examined the association between the presence of CCL and subsequent breast cancer risk in a nested case-control study of benign breast disease (BBD) and breast cancer within the Nurses' Health Studies (394 cases, 1,606 controls). Benign breast biopsy slides were reviewed by pathologists and CCL presence assessed. Logistic regression was used to compute odds ratios (ORs) and 95% confidence intervals (CIs) for the association between CCL and breast cancer risk. RESULTS: Women with CCL (140 cases, 448 controls) had an increased risk of breast cancer compared with those without CCL (OR = 1.44, 95% CI: 1.14 to 1.83), although this was attenuated and became non-significant after adjustment for the histologic category of BBD (OR = 1.20, 95% CI: 0.94 to 1.54). CCL presence was associated with the greatest risk of breast cancer for those with nonproliferative BBD (OR = 1.36, 95% CI: 0.79 to 2.37) and the lowest risk for those with atypical hyperplasia (AH) (OR = 1.10, 95% CI: 0.65 to 1.87); however, this apparent heterogeneity in risk across BBD categories was not significant (P for interaction between CCL presence and BBD category = 0.77). CONCLUSIONS: These results provide evidence that CCL may be an important marker of breast cancer risk in women with BBD but suggest that CCL do not increase breast cancer risk independently of concurrent proliferative changes in the breast.
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spelling pubmed-29496542010-10-06 Columnar cell lesions and subsequent breast cancer risk: a nested case-control study Aroner, Sarah A Collins, Laura C Schnitt, Stuart J Connolly, James L Colditz, Graham A Tamimi, Rulla M Breast Cancer Res Research Article INTRODUCTION: Histologic and genetic evidence suggests that at least some columnar cell lesions (CCL) of the breast represent precursor lesions in the low-grade breast neoplasia pathway. However, the risk of subsequent breast cancer associated with the presence of CCL in a benign breast biopsy is poorly understood. METHODS: The authors examined the association between the presence of CCL and subsequent breast cancer risk in a nested case-control study of benign breast disease (BBD) and breast cancer within the Nurses' Health Studies (394 cases, 1,606 controls). Benign breast biopsy slides were reviewed by pathologists and CCL presence assessed. Logistic regression was used to compute odds ratios (ORs) and 95% confidence intervals (CIs) for the association between CCL and breast cancer risk. RESULTS: Women with CCL (140 cases, 448 controls) had an increased risk of breast cancer compared with those without CCL (OR = 1.44, 95% CI: 1.14 to 1.83), although this was attenuated and became non-significant after adjustment for the histologic category of BBD (OR = 1.20, 95% CI: 0.94 to 1.54). CCL presence was associated with the greatest risk of breast cancer for those with nonproliferative BBD (OR = 1.36, 95% CI: 0.79 to 2.37) and the lowest risk for those with atypical hyperplasia (AH) (OR = 1.10, 95% CI: 0.65 to 1.87); however, this apparent heterogeneity in risk across BBD categories was not significant (P for interaction between CCL presence and BBD category = 0.77). CONCLUSIONS: These results provide evidence that CCL may be an important marker of breast cancer risk in women with BBD but suggest that CCL do not increase breast cancer risk independently of concurrent proliferative changes in the breast. BioMed Central 2010 2010-08-06 /pmc/articles/PMC2949654/ /pubmed/20691043 http://dx.doi.org/10.1186/bcr2624 Text en Copyright ©2010 Aroner et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Aroner, Sarah A
Collins, Laura C
Schnitt, Stuart J
Connolly, James L
Colditz, Graham A
Tamimi, Rulla M
Columnar cell lesions and subsequent breast cancer risk: a nested case-control study
title Columnar cell lesions and subsequent breast cancer risk: a nested case-control study
title_full Columnar cell lesions and subsequent breast cancer risk: a nested case-control study
title_fullStr Columnar cell lesions and subsequent breast cancer risk: a nested case-control study
title_full_unstemmed Columnar cell lesions and subsequent breast cancer risk: a nested case-control study
title_short Columnar cell lesions and subsequent breast cancer risk: a nested case-control study
title_sort columnar cell lesions and subsequent breast cancer risk: a nested case-control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949654/
https://www.ncbi.nlm.nih.gov/pubmed/20691043
http://dx.doi.org/10.1186/bcr2624
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