Statins and risk of cancer: A meta-analysis of randomized, double-blind, placebo-controlled trials

Indian J Cancer. 2017 Apr-Jun;54(2):470-477. doi: 10.4103/ijc.IJC_214_17.

Abstract

Purpose: Several meta-analyses of randomized controlled trials (RCTs) reported no association between the use of statins and the risk of cancer. However, they included open-label RCTs, which did not use placebo as a control group. This study aimed to evaluate the effect of statins on cancer risk using a meta-analysis of randomized, double-blind, placebo-controlled trials (RDBPCTs).

Methods: We searched PubMed, EMBASE, and the Cochrane Library in March 2016. Two individual authors reviewed and selected RDBPCTs based on selection criteria.

Results: Out of 676 retrieved articles, a total of 21 RDBPCTs with 65,196 participants (32,618 in the statin group and 32,578 in the placebo group) were included in the meta-analysis. Overall, we found that there was no significant association between the use of statins and the risk of cancer (relative risk 0.97, 95% confidence interval 0.92-1.02, I2 = 0.0%) in a fixed-effect meta-analysis. In addition, in the subgroup meta-analyses, no beneficial effect of statins was observed when analyzed by statin type, country, follow-up period, methodological quality, underlying diseases/population, and type of cancer.

Conclusions: The current meta-analysis of RDBPCTs found that there was no association between the use of statins and the risk of cancer.

Keywords: 3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors; cancer; meta-analysis; randomized controlled trials; statins.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Double-Blind Method
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / adverse effects*
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology
  • Middle Aged
  • Neoplasms / chemically induced*
  • Neoplasms / pathology
  • Risk
  • Young Adult

Substances

  • Hydroxymethylglutaryl-CoA Reductase Inhibitors