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The risks of cancer in older women with BRCA pathogenic variants: How far have we come?
Metcalfe, Kelly A; Gronwald, Jacek; Tung, Nadine M; McCuaig, Jeanna M; Eisen, Andrea; Elser, Christine; Foulkes, William D; Neuhausen, Susan L; Senter, Leigha; Moller, Pal; Bordeleau, Louise; Fruscio, Robert; Velsher, Lea; Zakalik, Dana; Olopade, Olufunmilayo I; Eng, Charis; Pal, Tuya; Cullinane, Carey A; Couch, Fergus J; Kotsopoulos, Joanne; Sun, Ping; Lubinski, Jan; Narod, Steven A.
Afiliación
  • Metcalfe KA; Women's College Research Institute, Women's College Hospital, Toronto, Ontario, Canada.
  • Gronwald J; Lawrence S. Bloomberg Faculty of Nursing, University of Toronto, Toronto, Ontario, Canada.
  • Tung NM; Departments of Genetics and Pathology, Pomeranian Medical University, Szczecin, Poland.
  • McCuaig JM; Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
  • Eisen A; Familial Cancer Clinic, Princess Margaret Hospital, University Health Network, Toronto, Ontario, Canada.
  • Elser C; Toronto-Sunnybrook Regional Cancer Center, Toronto, Ontario, Canada.
  • Foulkes WD; Marvelle Koffler Breast Centre, Mt. Sinai Hospital, Toronto, Ontario, Canada.
  • Neuhausen SL; Program in Cancer Genetics, Department of Oncology and Human Genetics, McGill University, Montréal, Quebec, Canada.
  • Senter L; Department of Population Sciences, Beckman Research Institute of City of Hope, Duarte, California, USA.
  • Moller P; Division of Human Genetics, the Ohio State University Medical Center, Comprehensive Cancer Center, Columbus, Ohio, USA.
  • Bordeleau L; Inherited Cancer Research Group, Department for Medical Genetics, Department of Tumor Biology, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.
  • Fruscio R; Department of Oncology, McMaster University, Hamilton, Ontario, Canada.
  • Velsher L; Department of Medicine and Surgery, University of Milan Bicocca, Monza, Italy.
  • Zakalik D; North York General Hospital, Toronto, Ontario, Canada.
  • Olopade OI; Cancer Genetics Program, Beaumont Hospitals, Royal Oak, Michigan, USA.
  • Eng C; Department of Medicine and Human Genetics, University of Chicago, Chicago, Illinois, USA.
  • Pal T; Genomic Medicine Institute, Cleveland Clinic, Cleveland, Ohio, USA.
  • Cullinane CA; Department of Medicine, Division of Genetic Medicine, Vanderbilt University Medical Center and the Vanderbilt-Ingram Cancer Center, Nashville, Tennessee, USA.
  • Couch FJ; MemorialCare Long Beach Medical Center, Long Beach, California, USA.
  • Kotsopoulos J; Division of Experimental Pathology and Laboratory Medicine, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
  • Sun P; Women's College Research Institute, Women's College Hospital, Toronto, Ontario, Canada.
  • Lubinski J; Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
  • Narod SA; Women's College Research Institute, Women's College Hospital, Toronto, Ontario, Canada.
Cancer ; 129(6): 901-907, 2023 03 15.
Article en En | MEDLINE | ID: mdl-36571512
ABSTRACT

BACKGROUND:

The purpose of this study was to estimate the cumulative risks of all cancers in women from 50 to 75 years of age with a BRCA1 or BRCA2 pathogenic variant.

METHODS:

Participants were women with BRCA1 or BRCA2 pathogenic variants from 85 centers in 16 countries. Women were eligible if they had no cancer before the age of 50 years. Participants completed a baseline questionnaire and follow-up questionnaires every 2 years. Women were followed from age 50 until a diagnosis of cancer, death, age 75, or last follow-up. The risk of all cancers combined from age 50 to 75 was estimated using the Kaplan-Meier method.

RESULTS:

There were 2211 women included (1470 BRCA1 and 742 BRCA2). There were 379 cancers diagnosed in the cohort between 50 and 75 years. The actuarial risk of any cancer from age 50 to 75 was 49% for BRCA1 and 43% for BRCA2. Breast (n = 186) and ovarian (n = 45) were the most frequent cancers observed. For women who had both risk-reducing mastectomy and bilateral salpingo-oophorectomy before age 50, the risk of developing any cancer between age 50 and 75 was 9%.

CONCLUSION:

Women with a BRCA1 or BRCA2 pathogenic variant have a high risk of cancer between the ages of 50 and 75 years and should be counselled appropriately.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteína BRCA1 / Predisposición Genética a la Enfermedad / Proteína BRCA2 Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Año: 2023 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteína BRCA1 / Predisposición Genética a la Enfermedad / Proteína BRCA2 Tipo de estudio: Etiology_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Año: 2023 Tipo del documento: Article País de afiliación: Canadá