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Established breast cancer risk factors by clinically important tumour characteristics

Breast cancer is a morphologically and clinically heterogeneous disease; however, it is less clear how risk factors relate to tumour features. We evaluated risk factors by tumour characteristics (histopathologic type, grade, size, and nodal status) in a population-based case–control of 2386 breast c...

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Autores principales: García-Closas, M, Brinton, L A, Lissowska, J, Chatterjee, N, Peplonska, B, Anderson, W F, Szeszenia-Dąbrowska, N, Bardin-Mikolajczak, A, Zatonski, W, Blair, A, Kalaylioglu, Z, Rymkiewicz, G, Mazepa-Sikora, D, Kordek, R, Lukaszek, S, Sherman, M E
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360503/
https://www.ncbi.nlm.nih.gov/pubmed/16755295
http://dx.doi.org/10.1038/sj.bjc.6603207
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author García-Closas, M
Brinton, L A
Lissowska, J
Chatterjee, N
Peplonska, B
Anderson, W F
Szeszenia-Dąbrowska, N
Bardin-Mikolajczak, A
Zatonski, W
Blair, A
Kalaylioglu, Z
Rymkiewicz, G
Mazepa-Sikora, D
Kordek, R
Lukaszek, S
Sherman, M E
author_facet García-Closas, M
Brinton, L A
Lissowska, J
Chatterjee, N
Peplonska, B
Anderson, W F
Szeszenia-Dąbrowska, N
Bardin-Mikolajczak, A
Zatonski, W
Blair, A
Kalaylioglu, Z
Rymkiewicz, G
Mazepa-Sikora, D
Kordek, R
Lukaszek, S
Sherman, M E
author_sort García-Closas, M
collection PubMed
description Breast cancer is a morphologically and clinically heterogeneous disease; however, it is less clear how risk factors relate to tumour features. We evaluated risk factors by tumour characteristics (histopathologic type, grade, size, and nodal status) in a population-based case–control of 2386 breast cancers and 2502 controls in Poland. Use of a novel extension of the polytomous logistic regression permitted simultaneous modelling of multiple tumour characteristics. Late age at first full-term birth was associated with increased risk of large (>2 cm) tumours (odds ratios (95% confidence intervals) 1.19 (1.07–1.33) for a 5-year increase in age), but not smaller tumours (P for heterogeneity adjusting for other tumour features (P(het))=0.007). On the other hand, multiparity was associated with reduced risk for small tumours (0.76 (0.68–0.86) per additional birth; P(het)=0.004). Consideration of all tumour characteristics simultaneously revealed that current or recent use of combined hormone replacement therapy was associated with risk of small (2.29 (1.66–3.15)) and grade 1 (3.36 (2.22–5.08)) tumours (P(het)=0.05 for size and 0.0008 for grade 1 vs 3), rather than specific histopathologic types (P(het)=0.63 for ductal vs lobular). Finally, elevated body mass index was associated with larger tumour size among both pre- and postmenopausal women (P(het)=0.05 and 0.0001, respectively). None of these relationships were explained by hormone receptor status of the tumours. In conclusion, these data support distinctive risk factor relationships by tumour characteristics of prognostic relevance. These findings might be useful in developing targeted prevention efforts.
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spelling pubmed-23605032009-09-10 Established breast cancer risk factors by clinically important tumour characteristics García-Closas, M Brinton, L A Lissowska, J Chatterjee, N Peplonska, B Anderson, W F Szeszenia-Dąbrowska, N Bardin-Mikolajczak, A Zatonski, W Blair, A Kalaylioglu, Z Rymkiewicz, G Mazepa-Sikora, D Kordek, R Lukaszek, S Sherman, M E Br J Cancer Epidemiology Breast cancer is a morphologically and clinically heterogeneous disease; however, it is less clear how risk factors relate to tumour features. We evaluated risk factors by tumour characteristics (histopathologic type, grade, size, and nodal status) in a population-based case–control of 2386 breast cancers and 2502 controls in Poland. Use of a novel extension of the polytomous logistic regression permitted simultaneous modelling of multiple tumour characteristics. Late age at first full-term birth was associated with increased risk of large (>2 cm) tumours (odds ratios (95% confidence intervals) 1.19 (1.07–1.33) for a 5-year increase in age), but not smaller tumours (P for heterogeneity adjusting for other tumour features (P(het))=0.007). On the other hand, multiparity was associated with reduced risk for small tumours (0.76 (0.68–0.86) per additional birth; P(het)=0.004). Consideration of all tumour characteristics simultaneously revealed that current or recent use of combined hormone replacement therapy was associated with risk of small (2.29 (1.66–3.15)) and grade 1 (3.36 (2.22–5.08)) tumours (P(het)=0.05 for size and 0.0008 for grade 1 vs 3), rather than specific histopathologic types (P(het)=0.63 for ductal vs lobular). Finally, elevated body mass index was associated with larger tumour size among both pre- and postmenopausal women (P(het)=0.05 and 0.0001, respectively). None of these relationships were explained by hormone receptor status of the tumours. In conclusion, these data support distinctive risk factor relationships by tumour characteristics of prognostic relevance. These findings might be useful in developing targeted prevention efforts. Nature Publishing Group 2006-07-03 2006-06-06 /pmc/articles/PMC2360503/ /pubmed/16755295 http://dx.doi.org/10.1038/sj.bjc.6603207 Text en Copyright © 2006 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 Epidemiology
García-Closas, M
Brinton, L A
Lissowska, J
Chatterjee, N
Peplonska, B
Anderson, W F
Szeszenia-Dąbrowska, N
Bardin-Mikolajczak, A
Zatonski, W
Blair, A
Kalaylioglu, Z
Rymkiewicz, G
Mazepa-Sikora, D
Kordek, R
Lukaszek, S
Sherman, M E
Established breast cancer risk factors by clinically important tumour characteristics
title Established breast cancer risk factors by clinically important tumour characteristics
title_full Established breast cancer risk factors by clinically important tumour characteristics
title_fullStr Established breast cancer risk factors by clinically important tumour characteristics
title_full_unstemmed Established breast cancer risk factors by clinically important tumour characteristics
title_short Established breast cancer risk factors by clinically important tumour characteristics
title_sort established breast cancer risk factors by clinically important tumour characteristics
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360503/
https://www.ncbi.nlm.nih.gov/pubmed/16755295
http://dx.doi.org/10.1038/sj.bjc.6603207
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