Estrogen plus progestin therapy and breast cancer in recently postmenopausal women

Am J Epidemiol. 2008 May 15;167(10):1207-16. doi: 10.1093/aje/kwn044. Epub 2008 Mar 27.

Abstract

The Women's Health Initiative trial found a modestly increased risk of invasive breast cancer with daily 0.625-mg conjugated equine estrogens plus 2.5-mg medroxyprogesterone acetate, with most evidence among women who had previously received postmenopausal hormone therapy. In comparison, observational studies mostly report a larger risk increase. To explain these patterns, the authors examined the effects of this regimen in relation to both prior hormone therapy and time from menopause to first use of postmenopausal hormone therapy ("gap time") in the Women's Health Initiative trial and in a corresponding subset of the Women's Health Initiative observational study. Postmenopausal women with a uterus enrolled at 40 US clinical centers during 1993-1998. The authors found that hazard ratios agreed between the two cohorts at a specified gap time and time from hormone therapy initiation. Combined trial and observational study data support an adverse effect on breast cancer risk. Women who initiate use soon after menopause, and continue for many years, appear to be at particularly high risk. For example, for a woman who starts soon after menopause and adheres to this regimen, estimated hazard ratios are 1.64 (95% confidence interval: 1.00, 2.68) over a 5-year period of use and 2.19 (95% confidence interval: 1.56, 3.08) over a 10-year period of use.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aged
  • Breast Neoplasms / chemically induced*
  • Breast Neoplasms / epidemiology
  • Cohort Studies
  • Estrogen Replacement Therapy / adverse effects*
  • Estrogens, Conjugated (USP) / administration & dosage
  • Estrogens, Conjugated (USP) / adverse effects*
  • Female
  • Humans
  • Medroxyprogesterone Acetate / administration & dosage
  • Medroxyprogesterone Acetate / adverse effects*
  • Middle Aged
  • Neoplasm Invasiveness
  • Observation
  • Postmenopause
  • Proportional Hazards Models
  • Randomized Controlled Trials as Topic
  • Risk
  • Time Factors

Substances

  • Estrogens, Conjugated (USP)
  • Medroxyprogesterone Acetate