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Published in: Clinical and Translational Oncology 12/2015

Open Access 01-12-2015 | Clinical Guides in Oncology

SEOM clinical guidelines in Hereditary Breast and ovarian cancer

Authors: G. Llort, I. Chirivella, R. Morales, R. Serrano, A. Beatriz Sanchez, A. Teulé, E. Lastra, J. Brunet, J. Balmaña, B. Graña, On behalf of the SEOM Hereditary Cancer Working Group

Published in: Clinical and Translational Oncology | Issue 12/2015

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Abstract

Approximately, 7 % of all breast cancers (BC) and 11–15 % of ovarian cancers (OC) are associated with inherited predisposition, mainly related to germline mutations in high penetrance BRCA1/2 genes. Clinical criteria for genetic testing are based on personal and family history to estimate a minimum 10 % detection rate. Selection criteria are evolving according to new advances in this field and the clinical utility of genetic testing. Multiplex panel testing carries its own challenges and we recommend inclusion of genes with clinical utility. We recommend screening with annual mammography from age 30 and breast MRI from age 25 for BRCA1 and BRCA2 mutation carriers. Bilateral salpingo-oophorectomy should be offered to women with a BRCA1 or BRCA2 mutation, between 35 and 40 years and after completion of childbearing, or individualise based on the earliest age of ovarian cancer diagnosed in the family. Bilateral risk-reducing mastectomy is an option for healthy BRCA1 and BRCA2 mutation carriers, as well as contralateral mastectomy for young patients with a prior BC diagnosis. BRCA genetic testing in patients with BC and OC may influence their locoregional and systemic treatment.
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Metadata
Title
SEOM clinical guidelines in Hereditary Breast and ovarian cancer
Authors
G. Llort
I. Chirivella
R. Morales
R. Serrano
A. Beatriz Sanchez
A. Teulé
E. Lastra
J. Brunet
J. Balmaña
B. Graña
On behalf of the SEOM Hereditary Cancer Working Group
Publication date
01-12-2015
Publisher
Springer Milan
Published in
Clinical and Translational Oncology / Issue 12/2015
Print ISSN: 1699-048X
Electronic ISSN: 1699-3055
DOI
https://doi.org/10.1007/s12094-015-1435-3

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