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Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study
BACKGROUND: The ‘common variant, common disease’ model predicts that a significant component of hereditary breast cancer unexplained by pathogenic variants in moderate or high-penetrance genes is due to the cumulative effect of common risk variants in DNA (polygenic risk). Assessing a woman’s breast...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516374/ https://www.ncbi.nlm.nih.gov/pubmed/28720130 http://dx.doi.org/10.1186/s12885-017-3485-0 |
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author | Yanes, Tatiane Meiser, Bettina Young, Mary-Anne Kaur, Rajneesh Mitchell, Gillian Barlow-Stewart, Kristine Roscioli, Tony Halliday, Jane James, Paul |
author_facet | Yanes, Tatiane Meiser, Bettina Young, Mary-Anne Kaur, Rajneesh Mitchell, Gillian Barlow-Stewart, Kristine Roscioli, Tony Halliday, Jane James, Paul |
author_sort | Yanes, Tatiane |
collection | PubMed |
description | BACKGROUND: The ‘common variant, common disease’ model predicts that a significant component of hereditary breast cancer unexplained by pathogenic variants in moderate or high-penetrance genes is due to the cumulative effect of common risk variants in DNA (polygenic risk). Assessing a woman’s breast cancer risk by testing for common risk variants can provide useful information for women who would otherwise receive uninformative results by traditional monogenic testing. Despite increasing support for the utility of common risk variants in hereditary breast cancer, research findings have not yet been integrated into clinical practice. Translational research is therefore critical to ensure results are effectively communicated, and that women do not experience undue adverse psychological outcomes. METHODS: In this prospective study, 400 women with a personal and/or high risk family history of breast cancer will be recruited from six familial cancer centers (FCCs) in Australia. Eligible women will be invited to attend a FCC and receive their personal polygenic risk result for breast cancer. Genetic health professionals participating in the study will receive training on the return of polygenic risk information and a training manual and visual aids will be developed to facilitate patient communication. Participants will complete up to three self-administered questionnaires over a 12-months period to assess the short-and long-term psychological and behavioral outcomes of receiving or not receiving their personal polygenic risk result. DISCUSSION: This is the world’s first study to assess the psychological and behavioral impact of offering polygenic risk information to women from families at high risk of breast cancer. Findings from this research will provide the basis for the development of a new service model to provide polygenic risk information in familial cancer clinics. TRIAL REGISTRATION: The study was retrospectively registered on 27th April 2017 with the Australian and New Zealand Clinical Trials Group (Registration no: ACTRN12617000594325; clinical trial URL: https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=372743). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-017-3485-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5516374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55163742017-07-20 Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study Yanes, Tatiane Meiser, Bettina Young, Mary-Anne Kaur, Rajneesh Mitchell, Gillian Barlow-Stewart, Kristine Roscioli, Tony Halliday, Jane James, Paul BMC Cancer Study Protocol BACKGROUND: The ‘common variant, common disease’ model predicts that a significant component of hereditary breast cancer unexplained by pathogenic variants in moderate or high-penetrance genes is due to the cumulative effect of common risk variants in DNA (polygenic risk). Assessing a woman’s breast cancer risk by testing for common risk variants can provide useful information for women who would otherwise receive uninformative results by traditional monogenic testing. Despite increasing support for the utility of common risk variants in hereditary breast cancer, research findings have not yet been integrated into clinical practice. Translational research is therefore critical to ensure results are effectively communicated, and that women do not experience undue adverse psychological outcomes. METHODS: In this prospective study, 400 women with a personal and/or high risk family history of breast cancer will be recruited from six familial cancer centers (FCCs) in Australia. Eligible women will be invited to attend a FCC and receive their personal polygenic risk result for breast cancer. Genetic health professionals participating in the study will receive training on the return of polygenic risk information and a training manual and visual aids will be developed to facilitate patient communication. Participants will complete up to three self-administered questionnaires over a 12-months period to assess the short-and long-term psychological and behavioral outcomes of receiving or not receiving their personal polygenic risk result. DISCUSSION: This is the world’s first study to assess the psychological and behavioral impact of offering polygenic risk information to women from families at high risk of breast cancer. Findings from this research will provide the basis for the development of a new service model to provide polygenic risk information in familial cancer clinics. TRIAL REGISTRATION: The study was retrospectively registered on 27th April 2017 with the Australian and New Zealand Clinical Trials Group (Registration no: ACTRN12617000594325; clinical trial URL: https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=372743). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-017-3485-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-07-18 /pmc/articles/PMC5516374/ /pubmed/28720130 http://dx.doi.org/10.1186/s12885-017-3485-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Yanes, Tatiane Meiser, Bettina Young, Mary-Anne Kaur, Rajneesh Mitchell, Gillian Barlow-Stewart, Kristine Roscioli, Tony Halliday, Jane James, Paul Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study |
title | Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study |
title_full | Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study |
title_fullStr | Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study |
title_full_unstemmed | Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study |
title_short | Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study |
title_sort | psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516374/ https://www.ncbi.nlm.nih.gov/pubmed/28720130 http://dx.doi.org/10.1186/s12885-017-3485-0 |
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