Cargando…
Familial risk of early and late onset cancer: nationwide prospective cohort study
Objective To determine whether familial risk of cancer is limited to early onset cases. Design Nationwide prospective cohort study. Setting Nationwide Swedish Family-Cancer Database. Participants All Swedes born after 1931 and their biological parents, totalling >12.2 million individuals, includi...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group Ltd.
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527651/ https://www.ncbi.nlm.nih.gov/pubmed/23257063 http://dx.doi.org/10.1136/bmj.e8076 |
_version_ | 1782253766751289344 |
---|---|
author | Kharazmi, E Fallah, M Sundquist, K Hemminki, K |
author_facet | Kharazmi, E Fallah, M Sundquist, K Hemminki, K |
author_sort | Kharazmi, E |
collection | PubMed |
description | Objective To determine whether familial risk of cancer is limited to early onset cases. Design Nationwide prospective cohort study. Setting Nationwide Swedish Family-Cancer Database. Participants All Swedes born after 1931 and their biological parents, totalling >12.2 million individuals, including >1.1 million cases of first primary cancer. Main outcome measures Familial risks of the concordant cancers by age at diagnosis. Results The highest familial risk was seen for offspring whose parents were diagnosed at an early age. Familial risks were significantly increased for colorectal, lung, breast, prostate, and urinary bladder cancer and melanoma, skin squamous cell carcinoma, and non-Hodgkin’s lymphoma, even when parents were diagnosed at age 70-79 or 80-89. When parents were diagnosed at more advanced ages (≥90), the risk of concordant cancer in offspring was still significantly increased for skin squamous cell carcinoma (hazard ratio 1.9, 95% confidence interval 1.4 to 2.7), colorectal (1.6, 1.2 to 2.0), breast (1.3, 1.0 to 1.6), and prostate cancer (1.3, 1.1 to 1.6). For offspring with a cancer diagnosed at ages 60-76 whose parents were affected at age <50, familial risks were not significantly increased for nearly all cancers. Conclusion Though the highest familial risks of cancer are seen in offspring whose parents received a diagnosis of a concordant cancer at earlier ages, increased risks exist even in cancers of advanced ages. Familial cancers might not be early onset in people whose family members were affected at older ages and so familial cancers might have distinct early and late onset components. |
format | Online Article Text |
id | pubmed-3527651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BMJ Publishing Group Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35276512012-12-21 Familial risk of early and late onset cancer: nationwide prospective cohort study Kharazmi, E Fallah, M Sundquist, K Hemminki, K BMJ Research Objective To determine whether familial risk of cancer is limited to early onset cases. Design Nationwide prospective cohort study. Setting Nationwide Swedish Family-Cancer Database. Participants All Swedes born after 1931 and their biological parents, totalling >12.2 million individuals, including >1.1 million cases of first primary cancer. Main outcome measures Familial risks of the concordant cancers by age at diagnosis. Results The highest familial risk was seen for offspring whose parents were diagnosed at an early age. Familial risks were significantly increased for colorectal, lung, breast, prostate, and urinary bladder cancer and melanoma, skin squamous cell carcinoma, and non-Hodgkin’s lymphoma, even when parents were diagnosed at age 70-79 or 80-89. When parents were diagnosed at more advanced ages (≥90), the risk of concordant cancer in offspring was still significantly increased for skin squamous cell carcinoma (hazard ratio 1.9, 95% confidence interval 1.4 to 2.7), colorectal (1.6, 1.2 to 2.0), breast (1.3, 1.0 to 1.6), and prostate cancer (1.3, 1.1 to 1.6). For offspring with a cancer diagnosed at ages 60-76 whose parents were affected at age <50, familial risks were not significantly increased for nearly all cancers. Conclusion Though the highest familial risks of cancer are seen in offspring whose parents received a diagnosis of a concordant cancer at earlier ages, increased risks exist even in cancers of advanced ages. Familial cancers might not be early onset in people whose family members were affected at older ages and so familial cancers might have distinct early and late onset components. BMJ Publishing Group Ltd. 2012-12-20 /pmc/articles/PMC3527651/ /pubmed/23257063 http://dx.doi.org/10.1136/bmj.e8076 Text en © Kharazmi et al 2012 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode. |
spellingShingle | Research Kharazmi, E Fallah, M Sundquist, K Hemminki, K Familial risk of early and late onset cancer: nationwide prospective cohort study |
title | Familial risk of early and late onset cancer: nationwide prospective cohort study |
title_full | Familial risk of early and late onset cancer: nationwide prospective cohort study |
title_fullStr | Familial risk of early and late onset cancer: nationwide prospective cohort study |
title_full_unstemmed | Familial risk of early and late onset cancer: nationwide prospective cohort study |
title_short | Familial risk of early and late onset cancer: nationwide prospective cohort study |
title_sort | familial risk of early and late onset cancer: nationwide prospective cohort study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527651/ https://www.ncbi.nlm.nih.gov/pubmed/23257063 http://dx.doi.org/10.1136/bmj.e8076 |
work_keys_str_mv | AT kharazmie familialriskofearlyandlateonsetcancernationwideprospectivecohortstudy AT fallahm familialriskofearlyandlateonsetcancernationwideprospectivecohortstudy AT sundquistk familialriskofearlyandlateonsetcancernationwideprospectivecohortstudy AT hemminkik familialriskofearlyandlateonsetcancernationwideprospectivecohortstudy |