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Hormonal Contraception and Breast Cancer Risk for Carriers of Germline Mutations in BRCA1 and BRCA2

  • Kelly Anne Phillips
  • , Joanne Kotsopoulos
  • , Susan M. Domchek
  • , Mary Beth Terry
  • , James A. Chamberlain
  • , Julie K. Bassett
  • , Amber M. Aeilts
  • , Irene L. Andrulis
  • , Saundra S. Buys
  • , Wanda Cui
  • , Mary B. Daly
  • , Andrea F. Eisen
  • , William D. Foulkes
  • , Michael L. Friedlander
  • , Jacek Gronwald
  • , John L. Hopper
  • , Esther M. John
  • , Beth Y. Karlan
  • , Raymond H. Kim
  • , Allison W. Kurian
  • Jan Lubinski, Kelly Metcalfe, Katherine L. Nathanson, Christian F. Singer, Melissa C. Southey, Heather Symecko, Nadine Tung, Steven A. Narod, Roger L. Milne
  • Peter Maccallum Cancer Centre
  • University of Melbourne
  • University of Toronto
  • University of Pennsylvania
  • Columbia University
  • Cancer Council Victoria
  • Ohio State University
  • University of Utah
  • McGill University
  • Royal Hospital for Women, Sydney
  • University of New South Wales
  • Pomeranian Medical University in Szczecin
  • Stanford University
  • University of California at Los Angeles
  • Princess Margaret Cancer Centre
  • Ontario Institute for Cancer Research
  • Medical University of Vienna
  • Monash University
  • Beth Israel Deaconess Medical Center

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

PURPOSE It is uncertain whether, and to what extent, hormonal contraceptives increase breast cancer (BC) risk for germline BRCA1 or BRCA2 mutation carriers.METHODS Using pooled observational data from four prospective cohort studies, associations between hormonal contraceptive use and BC risk for unaffected female BRCA1 and BRCA2 mutation carriers were assessed using Cox regression.RESULTSOf 3,882 BRCA1 and 1,509 BRCA2 mutation carriers, 53% and 71%, respectively, had ever used hormonal contraceptives for at least 1 year (median cumulative duration of use, 4.8 and 5.7 years, respectively). Overall, 488 BRCA1 and 191 BRCA2 mutation carriers developed BC during median follow-up of 5.9 and 5.6 years, respectively. Although for BRCA1 mutation carriers, neither current nor past use of hormonal contraceptives for at least 1 year was statistically significantly associated with BC risk (hazard ratio [HR], 1.40 [95% CI, 0.94 to 2.08], P =.10 for current use; 1.16 [0.80 to 1.69], P =.4, 1.40 [0.99 to 1.97], P =.05, and 1.27 [0.98 to 1.63], P =.07 for past use 1-5, 6-10, and >10 years before, respectively), ever use was associated with increased risk (HR, 1.29 [95% CI, 1.04 to 1.60], P =.02). Furthermore, BC risk increased with longer cumulative duration of use, with an estimated proportional increase in risk of 3% (1%-5%, P =.002) for each additional year of use. For BRCA2 mutation carriers, there was no evidence that current or ever use was associated with increased BC risk (HR, 0.70 [95% CI, 0.33 to 1.47], P =.3 and 1.07 [0.73 to 1.57], P =.7, respectively).CONCLUSION Hormonal contraceptives were associated with increased BC risk for BRCA1 mutation carriers, especially if used for longer durations. Decisions about their use in women with BRCA1 mutations should carefully weigh the risks and benefits for each individual.

Original languageEnglish
Pages (from-to)422-431
Number of pages10
JournalJournal of Clinical Oncology
Volume43
Issue number4
DOIs
StatePublished - Feb 1 2025

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/genetics
  • Female
  • Genes, BRCA1
  • Genes, BRCA2
  • Germ-Line Mutation
  • Heterozygote
  • Hormonal Contraception/adverse effects
  • Humans
  • Middle Aged
  • Prospective Studies
  • Risk Factors

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