Gandini Sara, Puntoni Matteo, Heckman-Stoddard Brandy M, Dunn Barbara K, Ford Leslie, DeCensi Andrea, Szabo Eva
Division of Epidemiology and Biostatistics, European Institute of Oncology, Milan, Italy.
Clinical Trials Office, Office of the Scientific Director, E.O. Ospedali Galliera, Genoa, Italy.
Cancer Prev Res (Phila). 2014 Sep;7(9):867-85. doi: 10.1158/1940-6207.CAPR-13-0424. Epub 2014 Jul 1.
Previous meta-analyses have shown that the antidiabetic agent metformin is associated with reduced cancer incidence and mortality. However, this effect has not been consistently demonstrated in animal models and recent epidemiologic studies. We performed a meta-analysis with a focus on confounders and biases, including body mass index (BMI), study type, and time-related biases. We identified 71 articles published between January 1, 1966, and May 31, 2013, through Pubmed, ISI Web of Science (Science Citation Index Expanded), Embase, and the Cochrane library that were related to metformin and cancer incidence or mortality. Study characteristics and outcomes were abstracted for each study that met inclusion criteria. We included estimates from 47 independent studies and 65,540 cancer cases in patients with diabetes. Overall cancer incidence was reduced by 31% [summary relative risk (SRR), 0.69; 95% confidence interval (CI), 0.52-0.90], although between-study heterogeneity was considerable (I(2) = 88%). Cancer mortality was reduced by 34% (SRR, 0.66; 95% CI, 0.54-0.81; I(2) = 21%). BMI-adjusted studies and studies without time-related biases also showed significant reduction in cancer incidence (SRR, 0.82; 95% CI, 0.70-0.96 with I(2) = 76% and SRR, 0.90; 95% CI, 0.89-0.91 with I(2) = 56%, respectively), albeit with lesser magnitude (18% and 10% reduction, respectively). However, studies of cancer mortality and individual organ sites did not consistently show significant reductions across all types of analyses. Although these associations may not be causal, our results show that metformin may reduce cancer incidence and mortality in patients with diabetes However, the reduction seems to be of modest magnitude and not affecting all populations equally. Clinical trials are needed to determine if these observations apply to nondiabetic populations and to specific organ sites.
以往的荟萃分析表明,抗糖尿病药物二甲双胍与癌症发病率和死亡率降低有关。然而,这种效应在动物模型和近期的流行病学研究中并未得到一致证实。我们进行了一项荟萃分析,重点关注混杂因素和偏倚,包括体重指数(BMI)、研究类型和时间相关偏倚。我们通过PubMed、ISI科学网(科学引文索引扩展版)、Embase和Cochrane图书馆,检索了1966年1月1日至2013年5月31日期间发表的71篇与二甲双胍和癌症发病率或死亡率相关的文章。对每项符合纳入标准的研究的特征和结果进行了摘要提取。我们纳入了47项独立研究的估计值以及65540例糖尿病患者的癌症病例。总体癌症发病率降低了31%[汇总相对风险(SRR),0.69;95%置信区间(CI),0.52 - 0.90],尽管研究间异质性相当大(I² = 88%)。癌症死亡率降低了34%(SRR,0.66;95%CI,0.54 - 0.81;I² = 21%)。经BMI调整的研究以及无时间相关偏倚的研究也显示癌症发病率显著降低(SRR分别为0.82;95%CI,0.70 - 0.96,I² = 76%和SRR,0.90;95%CI,0.89 - 0.91,I² = 56%),尽管降低幅度较小(分别降低18%和10%)。然而,癌症死亡率和各个器官部位的研究在所有类型的分析中并未一致显示出显著降低。尽管这些关联可能并非因果关系,但我们的结果表明二甲双胍可能降低糖尿病患者的癌症发病率和死亡率。然而,降低幅度似乎较小,且并非对所有人群都有同等影响。需要进行临床试验来确定这些观察结果是否适用于非糖尿病人群和特定器官部位。