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Breast Cancer Research
Erschienen in: Breast Cancer Research 6/2008

01.12.2008 | Review

Genetic counselling and testing for inherited gene mutations in newly diagnosed patients with breast cancer: a review of the existing literature and a proposed research agenda

verfasst von: Bettina Meiser, Kathy Tucker, Michael Friedlander, Kristine Barlow-Stewart, Elizabeth Lobb, Christobel Saunders, Gillian Mitchell

Erschienen in: Breast Cancer Research | Ausgabe 6/2008

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Abstract

Many women newly diagnosed with breast cancer and with a strong family history of breast cancer are referred to a family cancer service for genetic counselling and for consideration of genetic testing for germline mutations in cancer predisposition genes following completion of their cancer treatment. However, there is growing evidence that mutation status may influence treatment recommendations, and that there may be benefits in having 'treatment-focused genetic counselling and testing' available shortly after cancer diagnosis. This article reviews the literature that could inform the development of treatment-focused genetic counselling and testing, including: the rationale for genetic testing to aid with treatment decisions; the potential benefits of using mutation or risk status to tailor management; the criteria that may be used to identify patients most likely to carry germline mutations; and the evidence regarding women's decision-making regarding treatment-focused genetic counselling and testing and the associated psychological impact.
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Metadaten
Titel
Genetic counselling and testing for inherited gene mutations in newly diagnosed patients with breast cancer: a review of the existing literature and a proposed research agenda
verfasst von
Bettina Meiser
Kathy Tucker
Michael Friedlander
Kristine Barlow-Stewart
Elizabeth Lobb
Christobel Saunders
Gillian Mitchell
Publikationsdatum
01.12.2008
Verlag
BioMed Central
Erschienen in
Breast Cancer Research / Ausgabe 6/2008
Elektronische ISSN: 1465-542X
DOI
https://doi.org/10.1186/bcr2194

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