Genetic/familial high-risk assessment: Breast and ovarian, version 1.2014 Journal Article


Authors: Daly, M. B.; Pilarski, R.; Axilbund, J. E.; Buys, S. S.; Crawford, B.; Friedman, S.; Garber, J. E.; Horton, C.; Kaklamani, V.; Klein, C.; Kohlmann, W.; Kurian, A.; Litton, J.; Madlensky, L.; Marcom, P. K.; Merajver, S. D.; Offit, K.; Pal, T.; Pasche, B.; Reiser, G.; Shannon, K. M.; Swisher, E.; Voian, N. C.; Weitzel, J. N.; Whelan, A.; Wiesner, G. L.; Dwyer, M. A.; Kumar, R.
Article Title: Genetic/familial high-risk assessment: Breast and ovarian, version 1.2014
Abstract: During the past few years, several genetic aberrations that may contribute to increased risks for development of breast and/ or ovarian cancers have been identified. The NCCN Guidelines for Genetic/Familial High-Risk Assessment: Breast and Ovarian focus specifically on the assessment of genetic mutations in BRCA1/BRCA2, TP53, and PTEN, and recommend approaches to genetic testing/counseling and management strategies in individuals with these mutations. This portion of the NCCN Guidelines includes recommendations regarding diagnostic criteria and management of patients with Cowden Syndrome/ PTEN hamartoma tumor syndrome.
Journal Title: Journal of the National Comprehensive Cancer Network
Volume: 12
Issue: 9
ISSN: 1540-1405
Publisher: Harborside Press  
Date Published: 2014-09-01
Start Page: 1326
End Page: 1338
Language: English
PROVIDER: scopus
PUBMED: 25190698
DOI/URL:
Notes: Export Date: 3 November 2014 -- Source: Scopus
Citation Impact
MSK Authors
  1. Kenneth Offit
    788 Offit