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What is the lifetime risk of developing cancer?: the effect of adjusting for multiple primaries
BACKGROUND: The ‘lifetime risk’ of cancer is generally estimated by combining current incidence rates with current all-cause mortality (‘current probability’ method) rather than by describing the experience of a birth cohort. As individuals may get more than one type of cancer, what is generally est...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3172907/ https://www.ncbi.nlm.nih.gov/pubmed/21772332 http://dx.doi.org/10.1038/bjc.2011.250 |
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author | Sasieni, P D Shelton, J Ormiston-Smith, N Thomson, C S Silcocks, P B |
author_facet | Sasieni, P D Shelton, J Ormiston-Smith, N Thomson, C S Silcocks, P B |
author_sort | Sasieni, P D |
collection | PubMed |
description | BACKGROUND: The ‘lifetime risk’ of cancer is generally estimated by combining current incidence rates with current all-cause mortality (‘current probability’ method) rather than by describing the experience of a birth cohort. As individuals may get more than one type of cancer, what is generally estimated is the average (mean) number of cancers over a lifetime. This is not the same as the probability of getting cancer. METHODS: We describe a method for estimating lifetime risk that corrects for the inclusion of multiple primary cancers in the incidence rates routinely published by cancer registries. The new method applies cancer incidence rates to the estimated probability of being alive without a previous cancer. The new method is illustrated using data from the Scottish Cancer Registry and is compared with ‘gold-standard’ estimates that use (unpublished) data on first primaries. RESULTS: The effect of this correction is to make the estimated ‘lifetime risk’ smaller. The new estimates are extremely similar to those obtained using incidence based on first primaries. The usual ‘current probability’ method considerably overestimates the lifetime risk of all cancers combined, although the correction for any single cancer site is minimal. CONCLUSION: Estimation of the lifetime risk of cancer should either be based on first primaries or should use the new method. |
format | Online Article Text |
id | pubmed-3172907 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-31729072012-07-26 What is the lifetime risk of developing cancer?: the effect of adjusting for multiple primaries Sasieni, P D Shelton, J Ormiston-Smith, N Thomson, C S Silcocks, P B Br J Cancer Epidemiology BACKGROUND: The ‘lifetime risk’ of cancer is generally estimated by combining current incidence rates with current all-cause mortality (‘current probability’ method) rather than by describing the experience of a birth cohort. As individuals may get more than one type of cancer, what is generally estimated is the average (mean) number of cancers over a lifetime. This is not the same as the probability of getting cancer. METHODS: We describe a method for estimating lifetime risk that corrects for the inclusion of multiple primary cancers in the incidence rates routinely published by cancer registries. The new method applies cancer incidence rates to the estimated probability of being alive without a previous cancer. The new method is illustrated using data from the Scottish Cancer Registry and is compared with ‘gold-standard’ estimates that use (unpublished) data on first primaries. RESULTS: The effect of this correction is to make the estimated ‘lifetime risk’ smaller. The new estimates are extremely similar to those obtained using incidence based on first primaries. The usual ‘current probability’ method considerably overestimates the lifetime risk of all cancers combined, although the correction for any single cancer site is minimal. CONCLUSION: Estimation of the lifetime risk of cancer should either be based on first primaries or should use the new method. Nature Publishing Group 2011-07-26 2011-07-19 /pmc/articles/PMC3172907/ /pubmed/21772332 http://dx.doi.org/10.1038/bjc.2011.250 Text en Copyright © 2011 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 Sasieni, P D Shelton, J Ormiston-Smith, N Thomson, C S Silcocks, P B What is the lifetime risk of developing cancer?: the effect of adjusting for multiple primaries |
title | What is the lifetime risk of developing cancer?: the effect of adjusting for multiple primaries |
title_full | What is the lifetime risk of developing cancer?: the effect of adjusting for multiple primaries |
title_fullStr | What is the lifetime risk of developing cancer?: the effect of adjusting for multiple primaries |
title_full_unstemmed | What is the lifetime risk of developing cancer?: the effect of adjusting for multiple primaries |
title_short | What is the lifetime risk of developing cancer?: the effect of adjusting for multiple primaries |
title_sort | what is the lifetime risk of developing cancer?: the effect of adjusting for multiple primaries |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3172907/ https://www.ncbi.nlm.nih.gov/pubmed/21772332 http://dx.doi.org/10.1038/bjc.2011.250 |
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