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Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers.
Mavaddat, Nasim; Antoniou, Antonis C; Mooij, Thea M; Hooning, Maartje J; Heemskerk-Gerritsen, Bernadette A; Noguès, Catherine; Gauthier-Villars, Marion; Caron, Olivier; Gesta, Paul; Pujol, Pascal; Lortholary, Alain; Barrowdale, Daniel; Frost, Debra; Evans, D Gareth; Izatt, Louise; Adlard, Julian; Eeles, Ros; Brewer, Carole; Tischkowitz, Marc; Henderson, Alex; Cook, Jackie; Eccles, Diana; van Engelen, Klaartje; Mourits, Marian J E; Ausems, Margreet G E M; Koppert, Linetta B; Hopper, John L; John, Esther M; Chung, Wendy K; Andrulis, Irene L; Daly, Mary B; Buys, Saundra S; Benitez, Javier; Caldes, Trinidad; Jakubowska, Anna; Simard, Jacques; Singer, Christian F; Tan, Yen; Olah, Edith; Navratilova, Marie; Foretova, Lenka; Gerdes, Anne-Marie; Roos-Blom, Marie-José; Van Leeuwen, Flora E; Arver, Brita; Olsson, Håkan; Schmutzler, Rita K; Engel, Christoph; Kast, Karin; Phillips, Kelly-Anne.
Afiliação
  • Mavaddat N; Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, Strangeways Research Laboratory, Worts Causeway, University of Cambridge, Cambridge, CBI 8RN, UK. nm274@medschl.cam.ac.uk.
  • Antoniou AC; Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, Strangeways Research Laboratory, Worts Causeway, University of Cambridge, Cambridge, CBI 8RN, UK.
  • Mooij TM; Department of Epidemiology, Netherlands Cancer Institute, P.O. Box 90203, 1006 BE, Amsterdam, The Netherlands.
  • Hooning MJ; Department of Medical Oncology, Family Center Clinic, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Heemskerk-Gerritsen BA; Department of Medical Oncology, Family Center Clinic, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Noguès C; DASC, Oncogénétique Clinique, Institut Paoli-Calmettes, Marseille, France.
  • Gauthier-Villars M; Institut Curie, Service de Génétique, Paris, France.
  • Caron O; Département de Médecine Oncologique, Gustave Roussy Hôpital Universitaire, Villejuif, France.
  • Gesta P; Centre Hospitalier, Service Régional d'Oncologie Génétique Poitou-Charentes, Niort, France.
  • Pujol P; Unité d'Oncogénétique, CHU Arnaud de Villeneuve, Montpellier, France.
  • Lortholary A; Centre Catherine de Sienne, Service d'Oncologie Médicale, Nantes, France.
  • Barrowdale D; Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, Strangeways Research Laboratory, Worts Causeway, University of Cambridge, Cambridge, CBI 8RN, UK.
  • Frost D; Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, Strangeways Research Laboratory, Worts Causeway, University of Cambridge, Cambridge, CBI 8RN, UK.
  • Evans DG; Genomic Medicine, Manchester Academic Health Sciences Centre, Division of Evolution and Genomic Sciences, Manchester University, Central Manchester, University Hospitals NHS Foundation Trust, Manchester, UK.
  • Izatt L; Clinical Genetics, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Adlard J; Yorkshire Regional Genetics Service, Chapel Allerton Hospital and University of Leeds, Leeds, UK.
  • Eeles R; Oncogenetics Team, The Institute of Cancer Research and Royal Marsden NHS Foundation Trust, London, UK.
  • Brewer C; Department of Clinical Genetics, Royal Devon & Exeter Hospital, Exeter, UK.
  • Tischkowitz M; Academic Department of Medical Genetics, National Institute for Health Research Cambridge Biomedical Research Centre, University of Cambridge, Cambridge, UK.
  • Henderson A; Institute of Genetic Medicine, Centre for Life, Newcastle Upon Tyne Hospitals NHS Trust, Newcastle upon Tyne, UK.
  • Cook J; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Sheffield, UK.
  • Eccles D; University of Southampton Faculty of Medicine, Southampton University Hospitals NHS Trust, Southampton, UK.
  • van Engelen K; Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
  • Mourits MJE; Department of Gynaecological Oncology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Ausems MGEM; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Koppert LB; Department of Surgical Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Hopper JL; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, VIC, 3010, Australia.
  • John EM; Department of Medicine and Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA, USA.
  • Chung WK; Departments of Pediatrics and Medicine, Columbia University Medical Center, New York, NY, USA.
  • Andrulis IL; Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, NY, USA.
  • Daly MB; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
  • Buys SS; Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada.
  • Benitez J; Department of Medicine, Huntsman Cancer Institute, University of Utah Health Sciences Center, Salt Lake City, UT, USA.
  • Jakubowska A; Human Genetics Group and Genotyping Unit, CEGEN, Human Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
  • Simard J; Molecular Oncology Laboratory, Hospital Clinico San Carlos, IdISSC, CIBERONC (ISCIII), Madrid, Spain.
  • Singer CF; Department of Genetics and Pathology, Pomeranian Medical University, Unii Lubelskiej 1, Szczecin, Poland.
  • Tan Y; Independent Laboratory of Molecular Biology and Genetic Diagnostics, Pomeranian Medical University, Unii Lubelskiej 1, Szczecin, Poland.
  • Olah E; Genomics Center, Centre Hospitalier Universitaire de Québec, Université Laval Research Center, 2705 Laurier Boulevard, Quebec City, Quebec, Canada.
  • Navratilova M; Department of OB/GYN and Comprehensive Cancer Center, Medical University of Vienna, Waehringer Guertel 18-20, A 1090, Vienna, Austria.
  • Foretova L; Department of OB/GYN and Comprehensive Cancer Center, Medical University of Vienna, Waehringer Guertel 18-20, A 1090, Vienna, Austria.
  • Gerdes AM; Department of Molecular Genetics, National Institute of Oncology, Budapest, Hungary.
  • Roos-Blom MJ; Department of Cancer Epidemiology and Genetics, Masaryk Memorial Cancer Institute, Zluty kopec 7, 65653, Brno, Czech Republic.
  • Van Leeuwen FE; Department of Cancer Epidemiology and Genetics, Masaryk Memorial Cancer Institute, Zluty kopec 7, 65653, Brno, Czech Republic.
  • Arver B; Department of Clinical Genetics, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
  • Olsson H; Department of Epidemiology, Netherlands Cancer Institute, P.O. Box 90203, 1006 BE, Amsterdam, The Netherlands.
  • Schmutzler RK; Department of Epidemiology, Netherlands Cancer Institute, P.O. Box 90203, 1006 BE, Amsterdam, The Netherlands.
  • Engel C; The Department of Oncology and Pathology, Karolinska Institute, 171 76, Stockholm, Sweden.
  • Kast K; Department of Oncology, Lund University Hospital, Lund, Sweden.
  • Phillips KA; Department of Oncology, Lund University Hospital, Lund, Sweden.
Breast Cancer Res ; 22(1): 8, 2020 01 16.
Article em En | MEDLINE | ID: mdl-31948486
ABSTRACT

BACKGROUND:

The effect of risk-reducing salpingo-oophorectomy (RRSO) on breast cancer risk for BRCA1 and BRCA2 mutation carriers is uncertain. Retrospective analyses have suggested a protective effect but may be substantially biased. Prospective studies have had limited power, particularly for BRCA2 mutation carriers. Further, previous studies have not considered the effect of RRSO in the context of natural menopause.

METHODS:

A multi-centre prospective cohort of 2272 BRCA1 and 1605 BRCA2 mutation carriers was followed for a mean of 5.4 and 4.9 years, respectively; 426 women developed incident breast cancer. RRSO was modelled as a time-dependent covariate in Cox regression, and its effect assessed in premenopausal and postmenopausal women.

RESULTS:

There was no association between RRSO and breast cancer for BRCA1 (HR = 1.23; 95% CI 0.94-1.61) or BRCA2 (HR = 0.88; 95% CI 0.62-1.24) mutation carriers. For BRCA2 mutation carriers, HRs were 0.68 (95% CI 0.40-1.15) and 1.07 (95% CI 0.69-1.64) for RRSO carried out before or after age 45 years, respectively. The HR for BRCA2 mutation carriers decreased with increasing time since RRSO (HR = 0.51; 95% CI 0.26-0.99 for 5 years or longer after RRSO). Estimates for premenopausal women were similar.

CONCLUSION:

We found no evidence that RRSO reduces breast cancer risk for BRCA1 mutation carriers. A potentially beneficial effect for BRCA2 mutation carriers was observed, particularly after 5 years following RRSO. These results may inform counselling and management of carriers with respect to RRSO.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Proteína BRCA1 / Proteína BRCA2 / Salpingo-Ooforectomia / Mutação Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Middle aged Idioma: En Revista: Breast Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Proteína BRCA1 / Proteína BRCA2 / Salpingo-Ooforectomia / Mutação Tipo de estudo: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Middle aged Idioma: En Revista: Breast Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido