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

Author:

Mavaddat NasimORCID, ,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,Terry Mary Beth,Milne Roger L.,Goldgar David E.,Rookus Matti A.,Andrieu Nadine,Easton Douglas F., , , , , ,

Abstract

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.

Funder

Cancer Research UK

National Cancer Institute

German Cancer Aid

European program ERA-NET on Translational Cancer Research

Dutch Cancer Society

Genome Canada and the Canadian Institutes of Health Research

Publisher

Springer Science and Business Media LLC

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