Sandhu Narinder, Schetter Susann E, Liao Jason, Hartman Terryl J, Richie John P, McGinley John, Thompson Henry J, Prokopczyk Bogdan, DuBrock Cynthia, Signori Carina, Hamilton Christopher, Calcagnotto Ana, Trushin Neil, Aliaga Cesar, Demers Laurence M, El-Bayoumy Karam, Manni Andrea
Department of Medicine, Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania.
Department of Radiology, Penn State Milton S. Hershey Medical Center, Hershey, Pennsylvania.
Cancer Prev Res (Phila). 2016 Apr;9(4):275-82. doi: 10.1158/1940-6207.CAPR-15-0235. Epub 2015 Dec 29.
Preclinical data indicate that omega-3 fatty acids (n-3FA) potentiate the chemopreventive effect of the antiestrogen (AE) tamoxifen against mammary carcinogenesis. The role of n-3FA in breast cancer prevention in humans is controversial. Preclinical and epidemiologic data suggest that n-3FA may be preferentially protective in obese subjects. To directly test the protective effect of n-3FA against breast cancer, we conducted a 2-year, open-label randomized clinical trial in 266 healthy postmenopausal women (50% normal weight, 30% overweight, 20% obese) with high breast density (BD; ≥25%) detected on their routine screening mammograms. Eligible women were randomized to one of the following five groups (i) no treatment, control; (ii) raloxifene 60 mg; (iii) raloxifene 30 mg; (iv) n-3FA lovaza 4 g; and (v) lovaza 4 g plus raloxifene 30 mg. The 2-year change in BD, a validated biomarker of breast cancer risk, was the primary endpoint of the study. In subset analysis, we tested the prespecified hypothesis that body mass index (BMI) influences the relationship between plasma n-3FA on BD. While none of the interventions affected BD in the intention-to-treat analysis, increase in plasma DHA was associated with a decrease in absolute breast density but only in participants with BMI >29. Our results suggest that obese women may preferentially experience breast cancer risk reduction from n-3FA administration.
临床前数据表明,ω-3脂肪酸(n-3FA)可增强抗雌激素(AE)他莫昔芬对乳腺癌发生的化学预防作用。n-3FA在人类乳腺癌预防中的作用存在争议。临床前和流行病学数据表明,n-3FA可能对肥胖受试者具有优先保护作用。为了直接测试n-3FA对乳腺癌的保护作用,我们对266名健康的绝经后妇女进行了一项为期2年的开放标签随机临床试验,这些妇女在常规筛查乳房X光检查中发现乳房密度(BD;≥25%)较高(50%体重正常,30%超重,20%肥胖)。符合条件的妇女被随机分为以下五组之一:(i)不治疗,作为对照;(ii)雷洛昔芬60毫克;(iii)雷洛昔芬30毫克;(iv)n-3FA洛伐他汀4克;(v)洛伐他汀4克加雷洛昔芬30毫克。BD的2年变化是乳腺癌风险的有效生物标志物,是该研究的主要终点。在亚组分析中,我们测试了预先设定的假设,即体重指数(BMI)会影响血浆n-3FA与BD之间的关系。虽然在意向性分析中,没有一种干预措施影响BD,但血浆DHA的增加与绝对乳房密度的降低相关,但仅在BMI>29的参与者中如此。我们的结果表明,肥胖女性可能优先从n-3FA给药中降低乳腺癌风险。