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Sex hormone levels and risks of estrogen receptor-negative and estrogen receptor-positive breast cancers

  • Ghada N. Farhat
  • , Steven R. Cummings
  • , Rowan T. Chlebowski
  • , Neeta Parimi
  • , Jane A. Cauley
  • , Thomas E. Rohan
  • , Alison J. Huang
  • , Mara Vitolins
  • , F. Allan Hubbell
  • , Joann E. Manson
  • , Barbara B. Cochrane
  • , Dorothy S. Lane
  • , Jennifer S. Lee
  • California Pacific Medical Center
  • University of California at Los Angeles
  • University of Pittsburgh
  • Albert Einstein College of Medicine
  • University of California at San Francisco
  • Wake Forest University
  • University of California at Irvine
  • Harvard University
  • University of Washington
  • University of California at Davis

Research output: Contribution to journalArticlepeer-review

96 Scopus citations

Abstract

BackgroundEndogenous sex hormone levels are associated with risks of breast cancer overall and estrogen receptor (ER)-positive breast tumors; however, their associations with ER-negative tumors remain unclear.MethodsIn a case-cohort study within the Women's Health Initiative Observational Study among postmenopausal women aged 50-79 years, we examined associations between endogenous testosterone and estradiol levels and the risks of ER-negative and ER-positive breast cancers. Serum levels of bioavailable testosterone and estradiol were assessed at the baseline visit in 317 invasive breast cancer case subjects and in a subcohort of 594 women. Bioavailable sex hormone levels were calculated using the total hormone level and the sex hormone-binding globulin concentration (measured by radioimmunoassays and a chemiluminescent immunoassay, respectively). Cox proportional hazards regression was used for statistical analysis. All statistical tests were two-sided.ResultThe unadjusted absolute rates of ER-negative breast cancer for testosterone quartiles 1-4 were 0.34, 0.20, 0.23, and 0.21 per 10000 person-years, respectively. Compared with women in the lowest quartile of testosterone level, those in quartile 2 had a 56% lower risk of ER-negative cancer (hazard ratio [HR] = 0.44, 95% confidence interval [CI] = 0.23 to 0.85), those in quartile 3 had a 45% lower risk (HR = 0.55, 95% CI = 0.30 to 1.01), and those in quartile 4 had a 49% lower risk (HR = 0.51, 95% CI = 0.28 to 0.94), independent of other risk factors. Estradiol level was not associated with ER-negative breast cancer. ER-positive breast cancer risk increased with higher testosterone levels (Ptrend =. 04), but this trend was not statistically significant after adjustment for estradiol (Ptrend =. 15). ER-positive cancer risk was approximately twofold higher in women with estradiol levels in quartiles 2-4 compared with women in quartile 1, independent of risk factors.ConclusionHigher serum levels of bioavailable testosterone are associated with lower risks of ER-negative breast cancer in postmenopausal women.

Original languageEnglish
Pages (from-to)562-570
Number of pages9
JournalJournal of the National Cancer Institute
Volume103
Issue number7
DOIs
StatePublished - Apr 6 2011

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