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运动或二甲双胍对乳腺癌和结直肠癌炎症生物标志物的影响:一项随机试验。

Effect of Exercise or Metformin on Biomarkers of Inflammation in Breast and Colorectal Cancer: A Randomized Trial.

机构信息

Pennington Biomedical Research Center, Baton Rouge, Louisiana.

Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, New Orleans, Louisiana.

出版信息

Cancer Prev Res (Phila). 2020 Dec;13(12):1055-1062. doi: 10.1158/1940-6207.CAPR-20-0188. Epub 2020 Aug 28.

Abstract

Observational studies report that physical activity and metformin are associated with improved clinical outcome in patients with cancer. Inflammation is one biological mechanism hypothesized to mediate these associations. In this phase II, multicenter, 2 × 2 factorial trial, 139 patients with breast and colorectal cancer who completed standard therapy were randomized to one of four treatment groups for 12 weeks: exercise alone, metformin alone, exercise and metformin, or control. Inflammation outcomes included high-sensitivity C-reactive protein (hs-CRP), soluble tumor necrosis factor alpha receptor two (sTNFαR2), and IL6. The primary modeling strategy evaluated the trial product estimand that was quantified using a generalized linear mixed model. Compared with control, exercise alone reduced hs-CRP [-30.2%; 95% confidence interval (CI), -50.3, -1.0] and IL6 (-30.9%; 95% CI, -47.3, -9.5) but did not change sTNFαR2 (1.0%; 95% CI, -10.4, 13.9). Compared with control, metformin alone did not change hs-CRP (-13.9%; 95% CI, -40.0, 23.4), sTNFαR2 (-10.4%; 95% CI, -21.3, 2.0), or IL6 (-22.9%; 95% CI, -42.3, 2.0). Compared with control, exercise and metformin reduced sTNFαR2 (-13.1%; 95% CI, -22.9, -1.0) and IL6 (-38.7%; 95% CI, -52.3, -18.9) but did not change hs-CRP (-20.5%; 95% CI, -44.0, 12.7). The combination of exercise and metformin was not synergistic for hs-CRP, sTNFαR2, or IL6. In survivors of breast and colorectal cancer with low baseline physical activity and without type 2 diabetes, exercise and metformin reduced measures of inflammation that are associated with cancer recurrence and mortality.

摘要

观察性研究报告称,体力活动和二甲双胍与癌症患者的临床结局改善相关。炎症是一种被假设介导这些关联的生物学机制。在这项 II 期、多中心、2×2 析因试验中,139 名完成标准治疗的乳腺癌和结直肠癌患者被随机分配到四个治疗组中的一个,接受为期 12 周的治疗:单独运动、单独二甲双胍、运动和二甲双胍或对照组。炎症结局包括高敏 C 反应蛋白(hs-CRP)、可溶性肿瘤坏死因子-α受体 2(sTNFαR2)和 IL6。主要建模策略评估了使用广义线性混合模型量化的试验产品估计量。与对照组相比,单独运动可降低 hs-CRP[-30.2%;95%置信区间(CI),-50.3,-1.0]和 IL6[-30.9%;95%CI,-47.3,-9.5],但不改变 sTNFαR2(1.0%;95%CI,-10.4,13.9)。与对照组相比,单独使用二甲双胍不会改变 hs-CRP[-13.9%;95%CI,-40.0,23.4]、sTNFαR2[-10.4%;95%CI,-21.3,2.0]或 IL6[-22.9%;95%CI,-42.3,20.0]。与对照组相比,运动和二甲双胍联合使用可降低 sTNFαR2[-13.1%;95%CI,-22.9,-1.0]和 IL6[-38.7%;95%CI,-52.3,-18.9],但不改变 hs-CRP[-20.5%;95%CI,-44.0,12.7]。运动和二甲双胍联合使用对 hs-CRP、sTNFαR2 或 IL6 没有协同作用。在基线体力活动较低且没有 2 型糖尿病的乳腺癌和结直肠癌幸存者中,运动和二甲双胍可降低与癌症复发和死亡相关的炎症标志物。

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