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首页> 外文期刊>BMC Cancer >The ASAMET trial: a randomized, phase II, double-blind, placebo-controlled, multicenter, 2?×?2 factorial biomarker study of tertiary prevention with low-dose aspirin and metformin in stage I-III colorectal cancer patients
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The ASAMET trial: a randomized, phase II, double-blind, placebo-controlled, multicenter, 2?×?2 factorial biomarker study of tertiary prevention with low-dose aspirin and metformin in stage I-III colorectal cancer patients

机译:ASAMET试验:一项针对I-III期大肠癌患者低剂量阿司匹林和二甲双胍三级预防的随机,II期,双盲,安慰剂对照,多中心,2?×?2析因生物标志物研究

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Epidemiological studies and cardiovascular prevention trials have shown that low-dose aspirin can reduce colorectal cancer (CRC) incidence and mortality, including inhibition of distant metastases. Metformin has also been associated with decreased colon adenoma recurrence in clinical trials and lower CRC incidence and mortality in epidemiological studies in diabetics. While both drugs have been tested as single agents, their combination has not been tested in cancer prevention trials. This is a randomized, placebo-controlled, double-blind, 2?×?2 biomarker trial of aspirin and metformin to test the activity of either agent alone and the potential synergism of their combination on a set of surrogate biomarkers of colorectal carcinogenesis. After surgery, 160 patients with stage I-III CRC are randomly assigned in a four-arm trial to either aspirin (100?mg?day), metformin (850?mg bis in die), their combination, or placebo for one year. The primary endpoint biomarker is the change of IHC expression of nuclear factor kappa-B (NFκB) in the unaffected mucosa of proximal and distal colon obtained by multiple biopsies in two paired colonoscopies one year apart. Additional biomarkers will include: 1) the measurement of circulating IL-6, CRP and VEGF; 2) the IHC expression of tissue pS6K, p53, beta-catenin, PI3K; 3) the associations of genetic markers with treatment response as assessed by next generation sequencing of primary tumors; 4) the genomic profile of candidate genes, pathways, and overall genomic patterns in tissue biopsies by genome wide gene expression arrays; and 5) the evaluation of adenoma occurrence at 1?year. A favorable biomarker modulation by aspirin and metformin may provide important clues for a subsequent phase III adjuvant trial aimed at preventing second primary cancer, delaying recurrence and improving prognosis in patients with CRC. EudraCT Number: 2015–004824-77; ClinicalTrial.gov Identifier: NCT03047837 . Registered on February 1, 2017.
机译:流行病学研究和心血管疾病预防试验表明,小剂量阿司匹林可降低结直肠癌(CRC)的发生率和死亡率,包括抑制远处转移。在临床试验中,二甲双胍还与结肠腺瘤复发减少和糖尿病的流行病学研究中较低的CRC发生率和死亡率相关。虽然两种药物均已作为单一药物进行测试,但其组合尚未在癌症预防试验中进行测试。这是一项阿司匹林和二甲双胍的随机,安慰剂对照,双盲,2α×β2生物标志物试验,用于测试两种药物单独的活性以及它们的组合对结直肠癌发生的一系列替代生物标志物的潜在协同作用。手术后,在一项四组试验中,将160名I-III期CRC患者随机分配至阿司匹林(100?mg?日),二甲双胍(850?mg bis死亡),其组合或安慰剂治疗一年。主要终点生物标志物是每年两次通过两次配对结肠镜活检获得的近端和远端结肠未受影响的粘膜中核因子κB(NFκB)IHC表达的变化。其他生物标志物将包括:1)循环IL-6,CRP和VEGF的测量; 2)组织pS6K,p53,β-catenin,PI3K的IHC表达; 3)通过下一代原发肿瘤测序评估的遗传标志物与治疗反应的关系; 4)通过全基因组基因表达阵列在组织活检组织中候选基因,途径和整体基因组模式的基因组概况; 5)评估1年时发生的腺瘤。阿司匹林和二甲双胍对生物标志物的有利调节可能为随后的旨在预防第二原发癌,延缓复发和改善CRC患者预后的III期辅助试验提供重要线索。 EudraCT编号:2015–004824-77; ClinicalTrial.gov标识符:NCT03047837。 2017年2月1日注册。

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