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Heterogeneity of colorectal cancer risk by tumour characteristics: Large prospective study of UK women

Associations between behavioural and other personal factors and colorectal cancer risk have been reported to vary by tumour characteristics, but evidence is inconsistent. In a large UK‐based prospective study we examined associations of 14 postulated risk factors with colorectal cancer risk overall,...

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Autores principales: Burón Pust, Andrea, Alison, Rupert, Blanks, Roger, Pirie, Kirstin, Gaitskell, Kezia, Barnes, Isobel, Gathani, Toral, Reeves, Gillian, Beral, Valerie, Green, Jane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347941/
https://www.ncbi.nlm.nih.gov/pubmed/27859268
http://dx.doi.org/10.1002/ijc.30527
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author Burón Pust, Andrea
Alison, Rupert
Blanks, Roger
Pirie, Kirstin
Gaitskell, Kezia
Barnes, Isobel
Gathani, Toral
Reeves, Gillian
Beral, Valerie
Green, Jane
author_facet Burón Pust, Andrea
Alison, Rupert
Blanks, Roger
Pirie, Kirstin
Gaitskell, Kezia
Barnes, Isobel
Gathani, Toral
Reeves, Gillian
Beral, Valerie
Green, Jane
author_sort Burón Pust, Andrea
collection PubMed
description Associations between behavioural and other personal factors and colorectal cancer risk have been reported to vary by tumour characteristics, but evidence is inconsistent. In a large UK‐based prospective study we examined associations of 14 postulated risk factors with colorectal cancer risk overall, and across three anatomical sites and four morphological subtypes. Among 1.3 million women, 18,518 incident colorectal cancers were identified during 13.8 (SD 3.4) years follow‐up via record linkage to national cancer registry data. Cox regression yielded adjusted relative risks. Statistical significance was assessed using correction for multiple testing. Overall, colorectal cancer risk was significantly associated with height, body mass index (BMI), smoking, alcohol intake, physical activity, parity and menopausal hormone therapy use. For smoking there was substantial heterogeneity across morphological types; relative risks around two or greater were seen in current smokers both for signet ring cell and for neuroendocrine tumours. Obese women were also at higher risk for signet ring cell tumours. For adenocarcinomas, the large majority of colorectal cancers in the cohort, all risk factor associations were weak. There was little or no heterogeneity in risk between tumours of the right colon, left colon and rectum for any of the 14 factors examined. These epidemiological findings complement an emerging picture from molecular studies of possible different developmental pathways for different tumour types.
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spelling pubmed-53479412017-03-23 Heterogeneity of colorectal cancer risk by tumour characteristics: Large prospective study of UK women Burón Pust, Andrea Alison, Rupert Blanks, Roger Pirie, Kirstin Gaitskell, Kezia Barnes, Isobel Gathani, Toral Reeves, Gillian Beral, Valerie Green, Jane Int J Cancer Cancer Epidemiology Associations between behavioural and other personal factors and colorectal cancer risk have been reported to vary by tumour characteristics, but evidence is inconsistent. In a large UK‐based prospective study we examined associations of 14 postulated risk factors with colorectal cancer risk overall, and across three anatomical sites and four morphological subtypes. Among 1.3 million women, 18,518 incident colorectal cancers were identified during 13.8 (SD 3.4) years follow‐up via record linkage to national cancer registry data. Cox regression yielded adjusted relative risks. Statistical significance was assessed using correction for multiple testing. Overall, colorectal cancer risk was significantly associated with height, body mass index (BMI), smoking, alcohol intake, physical activity, parity and menopausal hormone therapy use. For smoking there was substantial heterogeneity across morphological types; relative risks around two or greater were seen in current smokers both for signet ring cell and for neuroendocrine tumours. Obese women were also at higher risk for signet ring cell tumours. For adenocarcinomas, the large majority of colorectal cancers in the cohort, all risk factor associations were weak. There was little or no heterogeneity in risk between tumours of the right colon, left colon and rectum for any of the 14 factors examined. These epidemiological findings complement an emerging picture from molecular studies of possible different developmental pathways for different tumour types. John Wiley and Sons Inc. 2017-01-18 2017-03-01 /pmc/articles/PMC5347941/ /pubmed/27859268 http://dx.doi.org/10.1002/ijc.30527 Text en © 2016 The Authors International Journal of Cancer published by John Wiley & Sons Ltd on behalf of Union for International Cancer Control This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cancer Epidemiology
Burón Pust, Andrea
Alison, Rupert
Blanks, Roger
Pirie, Kirstin
Gaitskell, Kezia
Barnes, Isobel
Gathani, Toral
Reeves, Gillian
Beral, Valerie
Green, Jane
Heterogeneity of colorectal cancer risk by tumour characteristics: Large prospective study of UK women
title Heterogeneity of colorectal cancer risk by tumour characteristics: Large prospective study of UK women
title_full Heterogeneity of colorectal cancer risk by tumour characteristics: Large prospective study of UK women
title_fullStr Heterogeneity of colorectal cancer risk by tumour characteristics: Large prospective study of UK women
title_full_unstemmed Heterogeneity of colorectal cancer risk by tumour characteristics: Large prospective study of UK women
title_short Heterogeneity of colorectal cancer risk by tumour characteristics: Large prospective study of UK women
title_sort heterogeneity of colorectal cancer risk by tumour characteristics: large prospective study of uk women
topic Cancer Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347941/
https://www.ncbi.nlm.nih.gov/pubmed/27859268
http://dx.doi.org/10.1002/ijc.30527
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