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Risk reduction strategies for BRCA1/2 hereditary ovarian cancer syndromes: a clinical practice guideline

OBJECTIVE: The purpose of this guideline is to make recommendations regarding the care of women who harbour a pathogenic or likely pathogenic variant in BRCA1 and BRCA2. METHODS: Draft recommendations were formulated based on evidence obtained through a systematic review of RCTs, comparative retrosp...

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Autores principales: Jacobson, Michelle, Coakley, Nadia, Bernardini, Marcus, Branco, Kelly-Ann, Elit, Laurie, Ferguson, Sarah, Kim, Raymond
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474940/
https://www.ncbi.nlm.nih.gov/pubmed/34565426
http://dx.doi.org/10.1186/s13053-021-00196-9
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author Jacobson, Michelle
Coakley, Nadia
Bernardini, Marcus
Branco, Kelly-Ann
Elit, Laurie
Ferguson, Sarah
Kim, Raymond
author_facet Jacobson, Michelle
Coakley, Nadia
Bernardini, Marcus
Branco, Kelly-Ann
Elit, Laurie
Ferguson, Sarah
Kim, Raymond
author_sort Jacobson, Michelle
collection PubMed
description OBJECTIVE: The purpose of this guideline is to make recommendations regarding the care of women who harbour a pathogenic or likely pathogenic variant in BRCA1 and BRCA2. METHODS: Draft recommendations were formulated based on evidence obtained through a systematic review of RCTs, comparative retrospective studies and guideline endorsement. The draft recommendations underwent an internal review by clinical and methodology experts, and an external review by clinical practitioners. RESULTS: The literature search yielded 1 guideline, 5 systematic reviews, and 15 studies that met the eligibility criteria. CONCLUSIONS: In women who harbour a pathogenic or likely pathogenic variant in BRCA1 and BRCA2 screening for ovarian cancer is not recommended. Risk-reducing surgery is recommended to reduce the risk of ovarian cancer. In the absence of contraindications, premenopausal women undergoing RRSO should be offered hormone therapy until menopause. Systemic hormone replacement therapy, is not recommended for women who have had a personal history of breast cancer. RRSO should be considered for breast cancer risk reduction in women younger than 50 years. After a breast cancer diagnosis, RRSO for breast cancer mortality reduction can be considered within two years to women who harbour a pathogenic or likely pathogenic variant in BRCA1 if younger than the recommended age range for ovarian cancer risk reduction. RRSO before the age of 40 and specifically for breast cancer treatment in BRCA2 should be considered only if recommended by their breast cancer oncologist. Following RRSO, it is not recommended to do surveillance for peritoneal cancer.
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spelling pubmed-84749402021-09-28 Risk reduction strategies for BRCA1/2 hereditary ovarian cancer syndromes: a clinical practice guideline Jacobson, Michelle Coakley, Nadia Bernardini, Marcus Branco, Kelly-Ann Elit, Laurie Ferguson, Sarah Kim, Raymond Hered Cancer Clin Pract Review OBJECTIVE: The purpose of this guideline is to make recommendations regarding the care of women who harbour a pathogenic or likely pathogenic variant in BRCA1 and BRCA2. METHODS: Draft recommendations were formulated based on evidence obtained through a systematic review of RCTs, comparative retrospective studies and guideline endorsement. The draft recommendations underwent an internal review by clinical and methodology experts, and an external review by clinical practitioners. RESULTS: The literature search yielded 1 guideline, 5 systematic reviews, and 15 studies that met the eligibility criteria. CONCLUSIONS: In women who harbour a pathogenic or likely pathogenic variant in BRCA1 and BRCA2 screening for ovarian cancer is not recommended. Risk-reducing surgery is recommended to reduce the risk of ovarian cancer. In the absence of contraindications, premenopausal women undergoing RRSO should be offered hormone therapy until menopause. Systemic hormone replacement therapy, is not recommended for women who have had a personal history of breast cancer. RRSO should be considered for breast cancer risk reduction in women younger than 50 years. After a breast cancer diagnosis, RRSO for breast cancer mortality reduction can be considered within two years to women who harbour a pathogenic or likely pathogenic variant in BRCA1 if younger than the recommended age range for ovarian cancer risk reduction. RRSO before the age of 40 and specifically for breast cancer treatment in BRCA2 should be considered only if recommended by their breast cancer oncologist. Following RRSO, it is not recommended to do surveillance for peritoneal cancer. BioMed Central 2021-09-26 /pmc/articles/PMC8474940/ /pubmed/34565426 http://dx.doi.org/10.1186/s13053-021-00196-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Jacobson, Michelle
Coakley, Nadia
Bernardini, Marcus
Branco, Kelly-Ann
Elit, Laurie
Ferguson, Sarah
Kim, Raymond
Risk reduction strategies for BRCA1/2 hereditary ovarian cancer syndromes: a clinical practice guideline
title Risk reduction strategies for BRCA1/2 hereditary ovarian cancer syndromes: a clinical practice guideline
title_full Risk reduction strategies for BRCA1/2 hereditary ovarian cancer syndromes: a clinical practice guideline
title_fullStr Risk reduction strategies for BRCA1/2 hereditary ovarian cancer syndromes: a clinical practice guideline
title_full_unstemmed Risk reduction strategies for BRCA1/2 hereditary ovarian cancer syndromes: a clinical practice guideline
title_short Risk reduction strategies for BRCA1/2 hereditary ovarian cancer syndromes: a clinical practice guideline
title_sort risk reduction strategies for brca1/2 hereditary ovarian cancer syndromes: a clinical practice guideline
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474940/
https://www.ncbi.nlm.nih.gov/pubmed/34565426
http://dx.doi.org/10.1186/s13053-021-00196-9
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