Considerations in genetic counseling for inherited breast cancer predisposition Journal Article


Authors: Robson, M. E.; Offit, K.
Article Title: Considerations in genetic counseling for inherited breast cancer predisposition
Abstract: Of the 190,000 women estimated to have been diagnosed with breast cancer in 2001, between 5% and 10% of them are likely to have developed their disease as the result of an inherited susceptibility. Although breast cancer is a component tumor of several familial cancer predisposition syndromes, mutations in BRCA1 and BRCA2 are the most commonly identified germline changes. Recognition of hereditary breast cancer is critical to allow the implementation of appropriate treatment, screening, and prevention strategies for the affected woman and her family members. Genetic testing may play an important role in refining risk assessment, identifying individuals at risk before cancer has developed, and relieving anxiety in family members who have not inherited the predisposition. Copyright 2002, Elsevier Science (USA). All rights reserved.
Keywords: major clinical study; mutation; review; cancer diagnosis; cancer incidence; cancer susceptibility; genetic predisposition to disease; cancer prevention; breast cancer; prevalence; risk factors; cancer screening; breast neoplasms; brca1 protein; brca2 protein; risk assessment; cancer genetics; germ line; genes, brca1; genes, brca2; genetic susceptibility; familial cancer; syndrome delineation; anxiety; disease predisposition; heterozygote detection; genetic counseling; inheritance; humans; human; female; priority journal
Journal Title: Seminars in Radiation Oncology
Volume: 12
Issue: 4
ISSN: 1053-4296
Publisher: Elsevier Inc.  
Date Published: 2002-10-01
Start Page: 362
End Page: 370
Language: English
DOI: 10.1053/srao.2002.35255
PUBMED: 12382194
PROVIDER: scopus
DOI/URL:
Notes: Export Date: 14 November 2014 -- Source: Scopus
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  1. Kenneth Offit
    788 Offit
  2. Mark E Robson
    676 Robson