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HORMONE REPLACEMENT THERAPY USE
IN RELATION TO TUMOR BIOLOGY AND
BREAST CANCER PROGNOSIS
[in Menopause - Hormones and CancerProceedings]
edited by M. Neves -e-Castro and B.G. Wren 2002
[MHC CH6 p49-53]
Outline and Commentary on the 2002 Proceedings
by Timothy D. Bilash MD, MS, OBGYN
June 2003
www.DrTimDelivers.com
Authors
H. Olsson [MHC CH 6]
Department of Oncology
University Hospital
Lund S-221 85
Sweden
- Hypothesis: age and differentiation of the breast epithelium at the time of initiation reflects tumor biology at eventual diagnosis
- more immature breast tissue gives more advanced tumors
- supported by findings that less advanced tumor stage has been found to be more common in HRT users
- more highly differentiated
- lower proliferation rate
- low histological grade
- p53-negative status
- more frequent estrgoen receptor positive status
- may be more lobular type tumor rather than ductal
- current HRT users may show a higher S-phase percentage
- Epidemiology
- highest risk for breast cancer seen for present use and low BMD
- [ANOTE] note that low BMD is associated with low serum estradiol
-
- Estrogen only seems to lower the risk
- continuous combined or sequential combined Estrogen effects are conflicting
- Sweden study shows increased breast cancer risk of diagnosis with
- breast cancer had 1.74 risk ratio with HRT
- no overall increased risk of total malignant tumors
- other cancers had lowered risk each alone was not statistically significant
- HRT was significantly associated with a lower risk of dying, longer survival (Odds Ratio = 0.78)
- notes
- cox regression analysis similar to WHI
- newly incident tumors
- [ISLT] need mortality rates for that year
- need a combined "other tumor" group to compare for statistical significance
- Research indicates that tumor biology and short-term prognosis are more favorable in breast cancer patients who have used HRT prior to diagnosis
- better survival for current HRT users
- breast cancer survival
- total survival
- this is irrespective of tumor stage, hormone receptor status, and tumor detection mode
- no survival benefit seen after 10 years from stopping for past HRT users
- family history and HRT exposure appear to be independent risk factors for breast cancer incidence
- reduced sensitivity and specificity in breast cancer screening would be opposite to a screening bias
- screening bias- HRT group would screen more often and find more tumors
- sensitivity bias- HRT group would find fewer tumors when screened, due to increased density
- tumor size bias- HRT group would find more tumors when screened, due to tumors that are already there are bigger (estrogen is a growth hormone for breast tissue)
- these would influence incidence data
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