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The risk of breast cancer in BRCA1 and BRCA2 mutation carriers without a first-degree relative with breast cancer.
Metcalfe, K A; Lubinski, J; Gronwald, J; Huzarski, T; McCuaig, J; Lynch, H T; Karlan, B; Foulkes, W D; Singer, C F; Neuhausen, S L; Senter, L; Eisen, A; Sun, P; Narod, S A.
Afiliação
  • Metcalfe KA; Lawrence S. Bloomberg Faculty of Nursing, University of Toronto, Toronto, Canada.
  • Lubinski J; Women's College Research Institute, Women's College Hospital, Toronto, Canada.
  • Gronwald J; Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.
  • Huzarski T; Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.
  • McCuaig J; Department of Genetics and Pathology, International Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.
  • Lynch HT; Division of Gynecologic Oncology, Princess Margaret Hospital, University Health Network, Toronto, Canada.
  • Karlan B; Department of Preventive Medicine and Public Health, Creighton University School of Medicine, Omaha, Nebraska.
  • Foulkes WD; Department of Gynecology and Oncology, Cedars Sinai Medical Center, Los Angeles, California.
  • Singer CF; Program in Cancer Genetics, Department of Oncology and Human Genetics, McGill University, Montreal, Canada.
  • Neuhausen SL; Department of Obstetrics and Gynecology and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
  • Senter L; Department of Population Sciences, Beckman Research Institute of City of Hope, Duarte, California.
  • Eisen A; Division of Human Genetics, Comprehensive Cancer Center, The Ohio State University Medical Center, Columbus, Ohio.
  • Sun P; Toronto-Sunnybrook Regional Cancer Center, Toronto, Canada.
  • Narod SA; Women's College Research Institute, Women's College Hospital, Toronto, Canada.
Clin Genet ; 93(5): 1063-1068, 2018 05.
Article em En | MEDLINE | ID: mdl-29206279
The objective of this study was to estimate the lifetime risk of breast cancer in women with a BRCA1 or BRCA2 mutation with and without at least 1 first-degree relative with breast cancer. A total of 2835 women with a BRCA1 or BRCA2 mutation were followed. Age- and gene-specific breast cancer rates were calculated. The relative risks of breast cancer for subjects with a family history of breast cancer, compared to no family history were calculated. The mean age at baseline was 41.1 years, and they were followed for a mean of 6.0 years. The estimated penetrance of breast cancer to age 80 years was 60.8% for BRCA1 and 63.1% for BRCA2. For all BRCA carriers, the penetrance of breast cancer to age 80 for those with no first-degree relative with breast cancer was 60.4% and 63.3% for those with at least 1 first-degree relative with breast cancer. The risk of breast cancer for BRCA carriers with no first-degree relative with breast cancer is substantial, and as a result, clinical management for these women should be the same as those for women with an affected relative.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Neoplasias da Mama / Proteína BRCA1 / Predisposição Genética para Doença / Proteína BRCA2 Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Neoplasias da Mama / Proteína BRCA1 / Predisposição Genética para Doença / Proteína BRCA2 Idioma: En Ano de publicação: 2018 Tipo de documento: Article