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Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: An international prospective cohort of BRCA1 and BRCA2 mutation carriers

  • Nasim Mavaddat
  • , Antonis C. Antoniou
  • , Thea M. Mooij
  • , Maartje J. Hooning
  • , Bernadette A. Heemskerk-Gerritsen
  • , Catherine Noguès
  • , Lilian Laborde
  • , Emmanuel Breysse
  • , Dominique Stoppa-Lyonnet
  • , Marion Gauthier-Villars
  • , Bruno Buecher
  • , Olivier Caron
  • , Emmanuelle Fourme-Mouret
  • , Jean Pierre Fricker
  • , Christine Lasset
  • , Valérie Bonadona
  • , Pascaline Berthet
  • , Laurence Faivre
  • , Elisabeth Luporsi
  • , Véronique Mari
  • Laurence Gladieff, Paul Gesta, Hagay Sobol, François Eisinger, Catherine Noguès, Michel Longy, Catherine Dugast, Chrystelle Colas, Isabelle Coupier, Pascal Pujol, Carole Corsini, Alain Lortholary, Philippe Vennin, Claude Adenis, Tan Dat Nguyen, Capucine Delnatte, Julie Tinat, Isabelle Tennevet, Jean Marc Limacher, Christine Maugard, Yves Jean Bignon, Liliane Demange, Clotilde Penet, Hélène Dreyfus, Odile Cohen-Haguenauer, Laurence Venat-Bouvet, Dominique Leroux, Hélène Dreyfus, Hélène Zattara-Cannoni, Sandra Fert-Ferrer, Odile Bera, Catherine Noguès, Marion Gauthier-Villars, Olivier Caron, Paul Gesta, Pascal Pujol, Alain Lortholary, Steve Ellis, Daniel Barrowdale, Debra Frost, D. Gareth Evans, Louise Izatt, Julian Adlard, Ros Eeles, Carole Brewer, Marc Tischkowitz, Alex Henderson, Jackie Cook, Diana Eccles, F. B.L. Hogervorst, J. M. Collée, C. J. Van Asperen, A. R. Mensenkamp, M. G.E.M. Ausems, H. E.J. Meijers-Heijboer, K. Van Engelen, M. J. Blok, J. C. Oosterwijk, J. Verloop, E. Van Den Broek, Klaartje Van Engelen, Marian J.E. Mourits, Margreet G.E.M. Ausems, Linetta B. Koppert, John L. Hopper, Esther M. John, Wendy K. Chung, Irene L. Andrulis, Mary B. Daly, Saundra S. Buys, Javier Benitez, Trinidad Caldes, Anna Jakubowska, Jacques Simard, Christian F. Singer, Yen Tan, Edith Olah, Marie Navratilova, Lenka Foretova, Anne Marie Gerdes, Marie José Roos-Blom, Flora E. Van Leeuwen, Brita Arver, Håkan Olsson, Rita K. Schmutzler, Christoph Engel, Karin Kast, Kelly Anne Phillips, Mary Beth Terry, Roger L. Milne, David E. Goldgar, Matti A. Rookus, Nadine Andrieu, Douglas F. Easton
  • University of Cambridge
  • Netherlands Cancer Institute
  • Erasmus University Rotterdam
  • Paoli-Institut Calmettes
  • Institut Curie
  • Université Paris-Sud
  • Centre Hospitalier, France
  • CHU Montpellier
  • Centre Catherine de Sienne
  • University of Manchester
  • Guy's and St Thomas' NHS Foundation Trust
  • University of Leeds
  • Royal Marsden NHS Foundation Trust
  • Royal Devon & Exeter NHS Foundation Trust
  • Newcastle upon Tyne Hospitals NHS Foundation Trust
  • Sheffield Children's NHS Foundation Trust
  • University of Southampton
  • Vrije Universiteit Amsterdam
  • University of Groningen
  • Utrecht University
  • University of Melbourne
  • Stanford University
  • Columbia University
  • University of Toronto
  • Sinai Health System
  • University of Utah
  • Peter Maccallum Cancer Centre
  • Biomedical Network on Rare Diseases (CIBERER)
  • Hospital Clínico San Carlos de Madrid
  • Pomeranian Medical University in Szczecin
  • Université Laval
  • Medical University of Vienna
  • National Institute of Oncology
  • Masaryk Memorial Cancer Institute
  • University of Copenhagen
  • Karolinska Institutet
  • Lund University
  • University Hospital of Cologne
  • University of Cologne
  • Leipzig University
  • Technische Universität Dresden
  • German Cancer Research Center
  • Cancer Council Victoria
  • Monash University
  • Genetic Epidemiology of Cancer team
  • Mines ParisTech
  • Université PSL

Research output: Contribution to journalArticlepeer-review

58 Scopus citations

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.

Original languageEnglish
Article number8
Pages (from-to)8
JournalBreast Cancer Research
Volume22
Issue number1
DOIs
StatePublished - Jan 16 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Adult
  • BRCA1 Protein/genetics
  • BRCA2 Protein/genetics
  • Breast Neoplasms/epidemiology
  • Cohort Studies
  • Female
  • Humans
  • Incidence
  • International Agencies
  • Menopause
  • Middle Aged
  • Mutation
  • Prospective Studies
  • Risk Reduction Behavior
  • Salpingo-oophorectomy/methods

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