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Effects of metformin on breast cancer

机译:二甲双胍对乳腺癌的影响

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Purpose: Metformin is associated with reduced breast cancer risk in observational studies in patients with diabetes, but clinical evidence for antitumor activity is unclear. The change in Ki-67 between pretreat-ment biopsy and post-treatment surgical specimen has prognostic value and may predict antitumor activity in breast cancer. Patients and Methods: After tumor biopsy, we randomly allocated 200 nondiabetic women with operable breast cancer to either metformin 850 mg/twice per day (n = 100) or placebo (n = 100). The primary outcome measure was the difference between arms in Ki-67 after 4 weeks adjusted for baseline values. Results: Overall, the metformin effect on Ki-67 change relative to placebo was not statistically significant, with a mean proportional increase of 4.0% (95% CI, -5.6% to 14.4%) 4 weeks apart. However, there was a different drug effect depending on insulin resistance (homeostasis model assessment [HOMA] index > 2.8, fasting glucose [mmol/L] x insulin [mU/L]/22.5; P(interaction) = .045), with a nonsignificant mean proportional decrease in Ki-67 of 10.5% (95% CI, -26.1% to!8.4%) in women with HOMA more than 2.8 and a nonsignificant increase of 11.1% (95% CI, -0.6% to 24.2%) with HOMA less than or equal to 2.8. A different effect of metformin according to HOMA index was noted also in luminal B tumors (P(interaction) = .05). Similar trends to drug effect modifications were observed according to body mass index (P = .143), waist/hip girth-ratio (P = .058), moderate alcohol consumption (P = .005), and C-reactive protein (P = .080). Conclusion: Metformin before surgery did not significantly affect Ki-67 overall, but showed significantly different effects according to insulin resistance, particularly in luminal B tumors. Our findings warrant further studies of metformin in breast cancer with careful consideration to the metabolic characteristics of the study population.
机译:目的:在糖尿病患者的观察性研究中,二甲双胍与降低乳腺癌风险有关,但抗肿瘤活性的临床证据尚不清楚。治疗前活检和治疗后手术标本之间Ki-67的变化具有预后价值,并可预测乳腺癌的抗肿瘤活性。患者和方法:肿瘤活检后,我们随机分配200名患有可手术性乳腺癌的非糖尿病女性,每天服用二甲双胍850 mg /两次(n = 100)或安慰剂(n = 100)。主要结局指标是调整基线值后4周后Ki-67两组之间的差异。结果:总体而言,相对于安慰剂,二甲双胍对Ki-67变化的影响无统计学意义,相隔4周平均比例增加4.0%(95%CI,-5.6%至14.4%)。但是,依胰岛素抵抗而有不同的药物作用(稳态模型评估[HOMA]指数> 2.8,空腹血糖[mmol / L] x胰岛素[mU / L] /22.5;P(相互作用)= .045), HOMA大于2.8的女性Ki-67的平均比例成比例下降10.5%(95%CI,-26.1%至!8.4%),无显着性增加11.1%(95%CI,-0.6%至24.2%) )且HOMA小于或等于2.8。根据HOMA指数,二甲双胍在管腔B肿瘤中也有不同的作用(P(相互作用)= 0.05)。根据体重指数(P = .143),腰围/臀围比(P = .058),适度饮酒(P = .005)和C反应蛋白(P = .080)。结论:术前二甲双胍总体上并未显着影响Ki-67,但根据胰岛素抵抗表现出明显不同的作用,特别是在管腔B型肿瘤中。我们的发现需要对二甲双胍在乳腺癌中进行进一步研究,同时要仔细考虑研究人群的代谢特征。

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