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Familial non-BRCA1/BRCA2-associated breast cancer

Familial non-BRCA1/BRCA2-associated breast cancer
Familial non-BRCA1/BRCA2-associated breast cancer
Multidisciplinary breast-cancer teams commonly encounter women, both premenopausal and postmenopausal, presenting with breast cancer who also have a family history of this disease. Much of the published work on management of hereditary breast cancer focuses on women with known mutations in BRCA1 and BRCA2, in whom high-grade tumours, common second primaries, and a differential response to adjuvant chemotherapies could be relevant in finding the most effective management strategies. Extrapolation of some of these findings to all patients with familial breast cancer is tempting. However, for women in whom BRCA1 or BRCA2 mutations are unlikely or not found, what evidence is there to inform choices about the various management options? We review the published work on management issues for patients with familial breast cancer not due to a detectable mutation in BRCA1/BRCA2 and compare it with the issues for BRCA1 and BRCA2 carriers on whom more information is available.
705-711
Eccles, D.M.
5b59bc73-11c9-4cf0-a9d5-7a8e523eee23
Pichert, G.
2bdde7cf-ac04-416f-b820-b0a833e6191f
Eccles, D.M.
5b59bc73-11c9-4cf0-a9d5-7a8e523eee23
Pichert, G.
2bdde7cf-ac04-416f-b820-b0a833e6191f

Eccles, D.M. and Pichert, G. (2005) Familial non-BRCA1/BRCA2-associated breast cancer. The Lancet Oncology, 6 (9), 705-711. (doi:10.1016/S1470-2045(05)70318-1).

Record type: Article

Abstract

Multidisciplinary breast-cancer teams commonly encounter women, both premenopausal and postmenopausal, presenting with breast cancer who also have a family history of this disease. Much of the published work on management of hereditary breast cancer focuses on women with known mutations in BRCA1 and BRCA2, in whom high-grade tumours, common second primaries, and a differential response to adjuvant chemotherapies could be relevant in finding the most effective management strategies. Extrapolation of some of these findings to all patients with familial breast cancer is tempting. However, for women in whom BRCA1 or BRCA2 mutations are unlikely or not found, what evidence is there to inform choices about the various management options? We review the published work on management issues for patients with familial breast cancer not due to a detectable mutation in BRCA1/BRCA2 and compare it with the issues for BRCA1 and BRCA2 carriers on whom more information is available.

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Published date: 2005

Identifiers

Local EPrints ID: 26288
URI: http://eprints.soton.ac.uk/id/eprint/26288
PURE UUID: 61f94dfa-3e10-416e-9453-e2bf55266622
ORCID for D.M. Eccles: ORCID iD orcid.org/0000-0002-9935-3169

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Date deposited: 20 Apr 2006
Last modified: 16 Mar 2024 02:39

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Contributors

Author: D.M. Eccles ORCID iD
Author: G. Pichert

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