Women's Health Research Program, School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Austin Health, Olivia Newton-John Cancer Centre, Heidelberg, Victoria, Australia.
Clin Endocrinol (Oxf). 2018 Nov;89(5):605-612. doi: 10.1111/cen.13830. Epub 2018 Sep 9.
We investigated whether metformin prevents tamoxifen-induced endometrial changes and insulin resistance (IR) after a diagnosis of breast cancer.
This was a single-centre, randomized, double-blind, placebo-controlled, parallel group trial. Postmenopausal women with hormone receptor-positive breast cancer taking tamoxifen were randomly allocated to metformin 850 mg or identical placebo, twice daily, for 52 weeks. Outcome measures included double endometrial thickness (ET) measured by transvaginal ultrasound, fasting insulin, glucose and IR estimated by the homeostasis model of assessment (HOMA-IR).
A total of 112 women were screened and 102 randomized. Results are presented as median (range). The 101 women who took at least one dose of medication were aged 56 (43-72) years, with 5(0.5-28) years postmenopause, and had taken tamoxifen for 28.9 (0-367.4) weeks. The baseline ET was 2.9 mm (1.4-21.9) for the placebo group (n = 52) and 2.5 mm (1.3-14.8) for the metformin group (n = 50). At 52 weeks, the median ET was statistically significantly lower for the metformin (n = 36) than for the placebo group (n = 45) (2.3 mm (1.4-7.8) vs 3.0 (1.2-11.3); P = 0.05). 13.3% allocated to placebo had an ET greater than 4 mm vs 5.7% for metformin (P = 0.26). There was no endometrial atypia or cancer. Compared with placebo, metformin resulted in significantly greater baseline-adjusted reductions in weight (P < 0.001), waist circumference (0.03) and HOMA-IR (P < 0.001).
Metformin appears to inhibit tamoxifen-induced endometrial changes and has favourable metabolic effects. Further research into the adjuvant use of metformin after breast cancer and to prevent EH and cancer is warranted.
我们研究了二甲双胍是否可以预防乳腺癌确诊后他莫昔芬引起的子宫内膜变化和胰岛素抵抗(IR)。
这是一项单中心、随机、双盲、安慰剂对照、平行组试验。正在服用他莫昔芬的激素受体阳性乳腺癌绝经后妇女被随机分配至二甲双胍 850mg 或相同的安慰剂,每日 2 次,共 52 周。主要结局包括经阴道超声测量的双层子宫内膜厚度(ET)、空腹胰岛素、血糖和通过评估稳态模型的胰岛素抵抗(HOMA-IR)。
共筛选了 112 名女性,其中 102 名被随机分组。结果以中位数(范围)表示。101 名至少服用一剂药物的女性年龄为 56(43-72)岁,绝经后 5(0.5-28)年,他莫昔芬治疗时间为 28.9(0-367.4)周。安慰剂组(n=52)的基线 ET 为 2.9mm(1.4-21.9),二甲双胍组(n=50)为 2.5mm(1.3-14.8)。52 周时,二甲双胍组(n=36)的 ET 中位数显著低于安慰剂组(n=45)(2.3mm(1.4-7.8)vs 3.0mm(1.2-11.3);P=0.05)。安慰剂组中 13.3%的 ET 大于 4mm,而二甲双胍组为 5.7%(P=0.26)。无子宫内膜非典型增生或癌症。与安慰剂相比,二甲双胍治疗后体重(P<0.001)、腰围(0.03)和 HOMA-IR 有显著的基线调整后降低(P<0.001)。
二甲双胍似乎可抑制他莫昔芬引起的子宫内膜变化,并具有良好的代谢作用。有必要进一步研究乳腺癌辅助应用二甲双胍预防子宫内膜增生和癌症。