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Blogger's Note: will be of interest to those with dual maligancies (endometrial/ovarian)and/or Lynch Syndrome patients
Abstract
Hormonal and reproductive factors modulate
bioavailable estrogen to influence endometrial cancer risk. Estrogen
affects the
microsatellite status of tumors, but the relation
between these estrogen-related factors and microsatellite status of
endometrial
tumors is not known. We evaluated associations
between hormonal and reproductive factors and risks of microsatellite
stable
(MSS) and microsatellite instable (MSI) endometrial
cancer among postmenopausal women (MSS cases=258, MSI cases=103 and
controls=742)
in a population-based case-control study in
Alberta, Canada (2002-2006)........ We observed a significant trend in risk reduction for MSI
(P-trend=0.005),
but not MSS (P-trend=0.23), cancer with oral
contraceptive (OC) use; with ≥5 years use, the risk reduction was
stronger for
MSI (OR=0.42, 95%CI=0.23-0.77) than for MSS cancer
(OR=0.80, 95%CI=0.54-1.17; P-heterogeneity=0.05). For more recent use
(<30
years), the risk reduction was stronger for MSI
(OR=0.36, 95%CI=0.19-0.69) than for MSS cancer (OR=0.77,
95%CI=0.51-1.15;
P-heterogeneity=0.032). No differential risk
associations were observed for menopausal hormone use, parity and age at
menarche,
menopause or first pregnancy. We found limited
evidence for statistical heterogeneity of associations of endometrial
cancer
risk with hormonal and reproductive factors by MSI
status, except with OC use. This finding suggests a potential role for
the MMR system in the reduction of endometrial
cancer risk associated with OC use, although the exact mechanism is
unclear.
This study shows for the first time that OC use is
associated with a reduced risk for MSI, but not for MSS, endometrial
cancer.
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