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Clinical Trial
. 2010 Oct;3(10):1342-50.
doi: 10.1158/1940-6207.CAPR-10-0022. Epub 2010 Aug 19.

Reduction in Ki-67 in benign breast tissue of high-risk women with the lignan secoisolariciresinol diglycoside

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Clinical Trial

Reduction in Ki-67 in benign breast tissue of high-risk women with the lignan secoisolariciresinol diglycoside

Carol J Fabian et al. Cancer Prev Res (Phila). 2010 Oct.

Abstract

Preclinical and correlative studies suggest reduced breast cancer with higher lignan intake or blood levels. We conducted a pilot study of modulation of risk biomarkers for breast cancer in premenopausal women after administration of the plant lignan secoisolariciresinol given as the diglycoside (SDG). Eligibility criteria included regular menstrual cycles, no oral contraceptives, a >3-fold increase in 5-year risk, and baseline Ki-67 of ≥2% in areas of hyperplasia in breast tissue sampled by random periareolar fine-needle aspiration (RPFNA) during the follicular phase of the menstrual cycle. SDG (50 mg/d) was given for 12 months, followed by repeat RPFNA. The primary end point was change in Ki-67. Secondary end points included change in cytomorphology, mammographic breast density, serum bioavailable estradiol and testosterone insulin-like growth factor-I and IGF-binding protein-3, and plasma lignan levels. Forty-five of 49 eligible women completed the study with excellent compliance (median = 96%) and few serious side effects (4% grade 3). Median plasma enterolactone increased ∼9-fold, and total lignans increased 16-fold. Thirty-six (80%) of the 45 evaluable subjects showed a decrease in Ki-67, from a median of 4% (range, 2-16.8%) to 2% (range, 0-15.2%; P < 0.001, Wilcoxon signed rank test). A decrease from baseline in the proportion of women with atypical cytology (P = 0.035) was also observed. Based on favorable risk biomarker modulation and lack of adverse events, we are initiating a randomized trial of SDG versus placebo in premenopausal women.

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Figures

Figure 1
Figure 1
Change in expression of Ki-67 assessed by immunocytochemistry over the course of the 12 month study. The difference in expression is statistically significant by Wilcoxon’s sign rank test.
Figure 2
Figure 2
Change in mammographic breast density (expressed as percent of breast area that is considered to be at increased density) over the course of the 12 month study. The triangles indicate subjects where density increased; the squares indicate subjects where density decreased. The dashed line indicates equivalence, i.e., no change over the course of the study. The difference in density is not statistically significant by Wilcoxon’s sign rank test.

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