Breast Cell Proliferation in Postmenopausal Women During HRT Evaluated Through Fine Needle Aspiration Cytology

In: Breast Cancer Research and Treatment · 2003 · vol. 78(2) , pp. 159–165 · doi:10.1023/a:1022987618445 · PMID:12725416 · W2017917796
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Hormone replacement therapy significantly increased breast cell proliferation in postmenopausal women, correlating with circulating estradiol and estrone levels.

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This prospective, double-blind, randomized study of postmenopausal women assessed breast epithelial cell proliferation during 6 months of continuous combined HRT using fine needle aspiration (FNA) cytology with immunocytochemical detection of MIB-1 (Ki-67) before and at 3 and 6 months. The total cohort (45 women completing; 135 biopsies) showed a more than 4-fold increase in proliferation from baseline to 3 months (mean MIB-1+ cells 2.2% to 9.1%, with some individuals up to 25%), with no further increase at 6 months. Proliferation correlated positively with circulating estradiol and estrone levels after 3 and 6 months, but not with other measured endogenous hormones, proteins, or with differences between the two exogenous progestogens (dienogest vs norethisterone). This paper relates to endometriosis and/or adenomyosis because the corpus includes it via upstream keyword matching rather than because the paper explicitly discusses endometriosis or adenomyosis.

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Abstract

The basis of breast cancer risk associated with hormonal therapies may lie in the regulation of cell proliferation. In a prospective, double-blind, randomized study postmenopausal women were given continuous combined hormone replacement therapy (HRT) either as estradiol valerate 2 mg/dienogest 2 mg, (E2V/DNG) or estradiol 2 mg/noretisterone acetate 1 mg (E2/NETA) for 6 months. Fine needle aspiration (FNA) biopsies were used for immunocytochemical analysis of breast cell proliferation before and during treatment. From 45 women completing the study 135 biopsies were obtained. In the total material there was a more than 4-fold increase in proliferation between baseline and 3 months (p < 0.001). The mean percentage of MIB-1 positive breast cells increased from 2.2 to 9.1%. In some individual women values were as high as 25%. No further increase was recorded at 6 months. While numerical values were somewhat lower in the E2V/DNG group, there were no significant differences between treatments. There was a positive correlation between breast cell proliferation (MIB-1%) and circulating levels of both estradiol (r s = 0.54, p < 0.01) and estrone (r s = 0.53, p < 0.01) after 3 and 6 months of treatment. No correlations with other endogenous hormones, proteins or with the two exogenous progestogens dienogest and norethisterone were observed. Increased breast cell proliferation should probably be regarded as an unwanted side-effect during HRT. Means to identify those women with the most pronounced proliferative response should be developed. The FNA biopsy technique may be a useful tool to monitor and evaluate the proliferative response to HRT in the normal breasts of postmenopausal women. Similar content being viewed by others

References

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