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Women's Decision Making about Risk‐Reducing Strategies in the Context of Hereditary Breast and Ovarian Cancer: A Systematic Review
Author(s) -
Howard A. Fuchsia,
Balneaves Lynda G.,
Bottorff Joan L.
Publication year - 2009
Publication title -
journal of genetic counseling
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.867
H-Index - 52
eISSN - 1573-3599
pISSN - 1059-7700
DOI - 10.1007/s10897-009-9245-9
Subject(s) - breast cancer , ovarian cancer , medicine , oophorectomy , context (archaeology) , gynecology , genetic counseling , prophylactic mastectomy , oncology , family medicine , mastectomy , cancer , hysterectomy , surgery , genetics , paleontology , biology
Women who have a mutation in the BRCA1 or BRCA2 genes have up to an 87% lifetime risk of breast cancer and up to a 40% lifetime risk of ovarian cancer. Cancer prevention and early detection strategies are often considered by these women to address this heightened risk. Risk‐reducing strategies include risk‐reducing mastectomy and oophorectomy, breast and ovarian cancer screening, and chemoprevention. This systematic literature review summarizes the factors and contexts that influence decision making related to cancer risk‐reducing strategies among women at high‐risk for hereditary breast and ovarian cancer. In the 43 published research articles reviewed, three main types of factors are identified that influence high‐risk women's decisions about risk‐reducing strategies: a) medical and physical factors, b) psychological factors and c) social context factors. How these factors operate in women's lives over time remains unknown, and would best be elucidated through prospective, longitudinal research, as well as qualitative research.