Abstract
The search for genes which predispose to inherited breast cancer has intensified with the cloning of the BRCA1 and BRCA2 genes. This presents doctors with a new dilemma in the management of healthy women, at very high risk but with no clinical evidence of a disease. For many years we have been able to identify an increased risk of developing breast cancer because of a family history and this has encouraged us to develop clinical trials of intervention strategies for these people. Clearly, the problems of conducting these trials will become more difficult when we are able to identify subgroups of healthy women at very high risk, in whom randomized clinical trials may be unacceptable. On the other hand, offering them untested treatments such as mastectomy, ovarian ablation or even tamoxifen is confounded by the risks that these interventions may be either ineffective or unnecessary.
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Powles, T.J., O’Brien, M.E.R., Davidson, T.I., Sacks, N.P.M. (1996). The management of women with a high risk of breast cancer. In: Eeles, R.A., Ponder, B.A.J., Easton, D.F., Horwich, A. (eds) Genetic Predisposition to Cancer. Springer, Boston, MA. https://doi.org/10.1007/978-1-4899-4501-3_17
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DOI: https://doi.org/10.1007/978-1-4899-4501-3_17
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