## Abstract ## BACKGROUND Observational studies and randomized trials have demonstrated that hormone replacement therapy (HRT) increases the recipient's risk of developing breast carcinoma. Because it is known that some breast malignancies are hormonally responsive and that others are not, it has
Short-term biologic response to withdrawal of hormone replacement therapy in patients with invasive breast carcinoma
โ Scribed by Ramachandran Prasad; Gary P. Boland; Angela Cramer; Elizabeth Anderson; W. Fiona Knox; Nigel J. Bundred
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 96 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0008-543X
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โฆ Synopsis
Abstract
BACKGROUND
The biologic effect of continuing hormone replacement therapy (HRT) after a diagnosis of breast carcinoma is unclear. The goal of rhe current study was to determine the shortโterm effect of HRT withdrawal on invasive breast carcinoma using biologic surrogate markers of tumor response.
METHODS
The study was performed between 1996 and 2000 and comprised 140 women who had been using HRT at the time of breast carcinoma diagnosis by core needle biopsy. The breast tumors were removed a median of 17 days later (range, 2โ31 days). Of these women, 125 women stopped HRT at the time of core needle biopsy and 15 continued to receive HRT until surgery. In addition, 55 women with breast carcinoma from the same time period, who were not receiving HRT at diagnosis, were studied. Changes in expression of Kiโ67 (a measure of epithelial cell proliferation), progesterone receptor (PR), p27^KIPโ1^ (a cyclinโdependent kinase inhibitor), and cyclin D1 (a cell cycleโrelated protein) were determined by immunohistochemistry on paired sections of the core needle biopsy and surgical specimens from each patient.
RESULTS
In women who stopped HRT, a significant decrease in Kiโ67 expression was observed between core needle biopsy and surgery in estrogen receptor (ER)โpositive (n = 106; P < 0.001), but not in ERโnegative tumors (n = 19; P = 0.58), with an associated reduction in PR (P < 0.001) and cyclin D1 expression (P < 0.001) and an increase in p27^KIPโ1^ (P = 0.03). These changes in Kiโ67 and PR expression occurred irrespective of cโerbโB2 status. No change was observed in any parameter in the other groups of patients.
CONCLUSIONS
ERโpositive invasive breast carcinomas demonstrated a favorable biologic response to withdrawal of HRT. Therefore, HRT should be stopped at the time of diagnosis and was subsequently contraindicated. Cancer 2003;98:2539โ46. ยฉ 2003 American Cancer Society.
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