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二甲双胍与安慰剂对加拿大癌症临床试验组 MA.32 中新原发性癌症的影响:早期乳腺癌 III 期随机双盲试验的二次分析。

Effect of Metformin Versus Placebo on New Primary Cancers in Canadian Cancer Trials Group MA.32: A Secondary Analysis of a Phase III Randomized Double-Blind Trial in Early Breast Cancer.

机构信息

Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, and Department of Medicine, University of Toronto, Toronto, ON, Canada.

Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada.

出版信息

J Clin Oncol. 2023 Dec 10;41(35):5356-5362. doi: 10.1200/JCO.23.00296. Epub 2023 Sep 11.

DOI:10.1200/JCO.23.00296
PMID:37695982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10713140/
Abstract

JCO Metformin has been associated with lower cancer risk in epidemiologic and preclinical research. In the MA.32 randomized adjuvant breast cancer trial, metformin ( placebo) did not affect invasive disease-free or overall survival. Here, we report metformin effects on the risk of new cancer. Between 2010 and 2013, 3,649 patients with breast cancer younger than 75 years without diabetes with high-risk T1-3, N0-3 M0 breast cancer (any estrogen receptor, progesterone receptor, human epidermal growth factor receptor 2) were randomly assigned to metformin 850 mg orally twice a day or placebo twice a day for 5 years. New primary invasive cancers (outside the ipsilateral breast) developing as a first event were identified. Time to events was described by the competing risks method; two-sided likelihood ratio tests adjusting for age, BMI, smoking, and alcohol intake were used to compare metformin versus placebo arms. A total of 184 patients developed new invasive cancers: 102 metformin and 82 placebo, hazard ratio (HR), 1.25; 95% CI, 0.94 to 1.68; = .13. These included 48 contralateral invasive breast cancers (27 metformin 21 placebo), HR, 1.29; 95% CI, 0.72 to 2.27; = .40 and 136 new nonbreast primary cancers (75 metformin 61 placebo), HR, 1.24; 95% CI, 0.88 to 1.74; = .21. Metformin did not reduce the risk of new cancer development in these nondiabetic patients with breast cancer.

摘要

JCO 二甲双胍在流行病学和临床前研究中与较低的癌症风险相关。在 MA.32 随机辅助乳腺癌试验中,二甲双胍(安慰剂)并未影响浸润性无病或总生存期。在这里,我们报告二甲双胍对新发癌症风险的影响。2010 年至 2013 年,3649 名年龄小于 75 岁、无糖尿病、具有高风险 T1-3、N0-3 M0 乳腺癌(任何雌激素受体、孕激素受体、人表皮生长因子受体 2)的乳腺癌患者被随机分配接受二甲双胍 850mg 口服,每日两次,或安慰剂每日两次,治疗 5 年。确定了首次发生的新原发性浸润性癌症(同侧乳房外)。采用竞争风险方法描述时间事件;采用双侧似然比检验,调整年龄、BMI、吸烟和饮酒摄入,比较二甲双胍与安慰剂组。共有 184 名患者发生新的浸润性癌症:102 名二甲双胍和 82 名安慰剂,风险比(HR)为 1.25;95%CI,0.94 至 1.68; =.13。其中包括 48 例对侧浸润性乳腺癌(27 例二甲双胍 21 例安慰剂),HR 为 1.29;95%CI,0.72 至 2.27; =.40 和 136 例新的非乳腺癌原发性癌症(75 例二甲双胍 61 例安慰剂),HR 为 1.24;95%CI,0.88 至 1.74; =.21。在这些无糖尿病的乳腺癌患者中,二甲双胍并未降低新发癌症的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fe/10713140/2d04735c1e33/jco-41-5356-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fe/10713140/2d04735c1e33/jco-41-5356-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fe/10713140/2d04735c1e33/jco-41-5356-g002.jpg

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