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Family history of colorectal cancer and survival: a Swedish population‐based study
OBJECTIVES: A family history of colorectal cancer (CRC) is an established risk factor for developing CRC, whilst the impact of family history on prognosis is unclear. The present study assessed the association between family history and prognosis and, based on current evidence, explored whether this...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318575/ https://www.ncbi.nlm.nih.gov/pubmed/32012369 http://dx.doi.org/10.1111/joim.13036 |
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author | Pesola, F. Eloranta, S. Martling, A. Saraste, D. Smedby, K. E. |
author_facet | Pesola, F. Eloranta, S. Martling, A. Saraste, D. Smedby, K. E. |
author_sort | Pesola, F. |
collection | PubMed |
description | OBJECTIVES: A family history of colorectal cancer (CRC) is an established risk factor for developing CRC, whilst the impact of family history on prognosis is unclear. The present study assessed the association between family history and prognosis and, based on current evidence, explored whether this association was modified by age at diagnosis. METHODS: Using data from the Swedish Colorectal Cancer Registry (SCRCR) linked with the Multigeneration Register and the National Cancer Register, we identified 31 801 patients with a CRC diagnosed between 2007 and 2016. The SCRCR is a clinically rich database which includes information on the cancer stage, grade, location, treatment, complications and postoperative follow‐up. RESULTS: We estimated excess mortality rate ratios (EMRR) for relative survival and hazard ratios (HR) for disease‐free survival with 95% confidence intervals (CIs) using flexible parametric models. We found no association between family history and relative survival (EMRR = 0.96, 95% CIs: 0.89–1.03, P = 0.21) or disease‐free survival (HR = 0.98, 95% CIs: 0.91–1.06, P = 0.64). However, age was found to modify the impact of family history on prognosis. Young patients (<50 at diagnosis) with a positive family history had less advanced (i.e. stages I and II) cancers than those with no family history (OR = 0.71, 95% CI: 0.56–0.89, P = 0.004) and lower excess mortality even after adjusting for cancer stage (EMMR = 0.63, 95% CIs: 0.47–0.84, P = 0.002). CONCLUSIONS: Our results suggest that young individuals with a family history of CRC may have greater health awareness, attend opportunistic screening and adopt lifestyle changes, leading to earlier diagnosis and better prognosis. |
format | Online Article Text |
id | pubmed-7318575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73185752020-06-29 Family history of colorectal cancer and survival: a Swedish population‐based study Pesola, F. Eloranta, S. Martling, A. Saraste, D. Smedby, K. E. J Intern Med Original Articles OBJECTIVES: A family history of colorectal cancer (CRC) is an established risk factor for developing CRC, whilst the impact of family history on prognosis is unclear. The present study assessed the association between family history and prognosis and, based on current evidence, explored whether this association was modified by age at diagnosis. METHODS: Using data from the Swedish Colorectal Cancer Registry (SCRCR) linked with the Multigeneration Register and the National Cancer Register, we identified 31 801 patients with a CRC diagnosed between 2007 and 2016. The SCRCR is a clinically rich database which includes information on the cancer stage, grade, location, treatment, complications and postoperative follow‐up. RESULTS: We estimated excess mortality rate ratios (EMRR) for relative survival and hazard ratios (HR) for disease‐free survival with 95% confidence intervals (CIs) using flexible parametric models. We found no association between family history and relative survival (EMRR = 0.96, 95% CIs: 0.89–1.03, P = 0.21) or disease‐free survival (HR = 0.98, 95% CIs: 0.91–1.06, P = 0.64). However, age was found to modify the impact of family history on prognosis. Young patients (<50 at diagnosis) with a positive family history had less advanced (i.e. stages I and II) cancers than those with no family history (OR = 0.71, 95% CI: 0.56–0.89, P = 0.004) and lower excess mortality even after adjusting for cancer stage (EMMR = 0.63, 95% CIs: 0.47–0.84, P = 0.002). CONCLUSIONS: Our results suggest that young individuals with a family history of CRC may have greater health awareness, attend opportunistic screening and adopt lifestyle changes, leading to earlier diagnosis and better prognosis. John Wiley and Sons Inc. 2020-03-03 2020-06 /pmc/articles/PMC7318575/ /pubmed/32012369 http://dx.doi.org/10.1111/joim.13036 Text en © 2020 The Authors. Journal of Internal Medicine published by John Wiley & Sons Ltd on behalf of Association for Publication of The Journal of Internal Medicine This is an open access article under the terms of the 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 | Original Articles Pesola, F. Eloranta, S. Martling, A. Saraste, D. Smedby, K. E. Family history of colorectal cancer and survival: a Swedish population‐based study |
title | Family history of colorectal cancer and survival: a Swedish population‐based study |
title_full | Family history of colorectal cancer and survival: a Swedish population‐based study |
title_fullStr | Family history of colorectal cancer and survival: a Swedish population‐based study |
title_full_unstemmed | Family history of colorectal cancer and survival: a Swedish population‐based study |
title_short | Family history of colorectal cancer and survival: a Swedish population‐based study |
title_sort | family history of colorectal cancer and survival: a swedish population‐based study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318575/ https://www.ncbi.nlm.nih.gov/pubmed/32012369 http://dx.doi.org/10.1111/joim.13036 |
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