DESCRIPTION: (Adapted from Investigator's Abstract) Epidemiologic studies
find that increased mammographic density is an independent risk factor for
breast cancer and the magnitude of risk associated with mammographic density
is greater than that associated with almost all other known risk factors for
breast cancer. This application focuses on 3 major questions: 1) are
endogenous levels of sex steroids in postmenopausal women related to
mammographic density; 2) does treatment with postmenopausal estrogen and
estrogen/progestin therapy increase mammographic density; and 3) do the
serum levels of estrone achieved as a result of treatment with
postmenopausal hormone therapy predict change in mammographic density? To
address these questions, the amount of density of mammograms performed
during the Postmenopausal Estrogen/Progestin Interventions (PEPI) Trial will
be determined using a computer-based threshold technique. PEPI was a
3-year, randomized placebo controlled trial of conjugated equine estrogens
(CEE) vs. CEE plus one of 3 progestin regimens, which enrolled 875
postmenopausal women aged 45-64 at baseline. Data already collected as part
of PEPI that will be used in this project will include: endogenous sex
steroids at baseline, PEPI treatment assignment, estrone serum levels
on-treatment, and necessary covariates. The project will last 3 years and
take place at 3 sites: UCLA, USC, and Bowman Gray. The specific aims are
to: 1) measure the density of mammograms performed at baseline and 12
months; 2) determine whether baseline mammographic density is associated
with endogenous levels of sex steroids; 3) quantify the relation between
change in mammographic density and adherence to treatments; and 4) determine
whether changes density are associated with serum levels of estrone achieved
as a result of hormone therapy. By assessing density changes in mammograms
with this computer-based method, which has been previously linked to a
quantified increase in risk of breast cancer, it may be possible to assess
how much of a risk-increase would be predicted by hormone use. The
investigators state that this may serve as the first in a series of
investigations that would allow identification of those women at higher risk
of developing breast toxicity from postmenopausal supplemental hormone use.
Error Notice
The database may currently be offline for maintenance and should be operational soon. If not, we have been notified of this error and will be reviewing it shortly.
We apologize for the inconvenience.
- The DCCPS Team.