Bonovas Stefanos, Filioussi Kalitsa, Tsavaris Nikolaos, Sitaras Nikolaos M
Department of Pharmacology, School of Medicine, University of Athens, Greece.
J Clin Oncol. 2006 Oct 20;24(30):4808-17. doi: 10.1200/JCO.2006.06.3560. Epub 2006 Sep 25.
A growing body of literature suggests that statins may have chemopreventive potential against cancer. Our aim was to examine the strength of this association through a detailed meta-analysis and meta-regression analysis of randomized controlled trials (RCTs).
A comprehensive search for trials published up to 2005 was performed, reviews of each study were conducted, and data were abstracted. Before meta-analysis, the studies were evaluated for publication bias and heterogeneity. Pooled relative risk (RR) estimates and 95% CIs were calculated using the random- and fixed-effects models. Subgroup, sensitivity, and meta-regression analyses were also conducted.
Thirty-five RCTs of statins for cardiovascular outcomes contributed to the analysis (n = 109,143). The degree of variability between trials was consistent with what would be expected to occur by chance alone. Statin use was not associated with a substantially increased or decreased overall risk of cancer (RR = 0.99; 95% CI, 0.94 to 1.04). Similarly, statin use did not significantly affect respiratory cancer risk (RR = 0.95; 95% CI, 0.83 to 1.09). However, the meta-regression analysis indicated that age of study participants modified the association between statin use and cancer risk (P = .003).
Our findings do not support a protective effect of statins against cancer. However, this conclusion is limited by the relatively short follow-up periods (4.5 years on average) of the studies analyzed. Thus, it is important to continue monitoring the long-term safety profiles of statins. Until then, physicians need to be vigilant in ensuring that statin use remains restricted to the approved indications.
越来越多的文献表明,他汀类药物可能具有预防癌症的化学预防潜力。我们的目的是通过对随机对照试验(RCT)进行详细的荟萃分析和荟萃回归分析来检验这种关联的强度。
对截至2005年发表的试验进行全面检索,对每项研究进行综述,并提取数据。在进行荟萃分析之前,对研究进行发表偏倚和异质性评估。使用随机效应模型和固定效应模型计算合并相对风险(RR)估计值和95%置信区间(CI)。还进行了亚组分析、敏感性分析和荟萃回归分析。
35项关于他汀类药物用于心血管结局的RCT纳入了分析(n = 109,143)。试验之间的变异程度与仅由偶然因素导致的预期情况一致。使用他汀类药物与癌症总体风险的显著增加或降低无关(RR = 0.99;95% CI,0.94至1.04)。同样,使用他汀类药物对呼吸道癌症风险没有显著影响(RR = 0.95;95% CI,0.83至1.09)。然而,荟萃回归分析表明,研究参与者的年龄改变了他汀类药物使用与癌症风险之间的关联(P = .003)。
我们的研究结果不支持他汀类药物对癌症具有保护作用。然而,这一结论受到所分析研究相对较短的随访期(平均4.5年)的限制。因此,继续监测他汀类药物的长期安全性概况很重要。在此之前,医生需要警惕确保他汀类药物的使用仍限于批准的适应症。