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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...

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Autores principales: Yanes, Tatiane, Meiser, Bettina, Young, Mary-Anne, Kaur, Rajneesh, Mitchell, Gillian, Barlow-Stewart, Kristine, Roscioli, Tony, Halliday, Jane, James, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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.
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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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