Bjerre L M, LeLorier J
Department of Epidemiology and Biostatistics, McGill University, Montréal, Quebec, Canada.
Am J Med. 2001 Jun 15;110(9):716-23. doi: 10.1016/s0002-9343(01)00705-7.
Although the short-term safety and tolerability of statins has been well established, their potential carcinogenicity in the long term is still debated. The goal of this study was to determine whether long-term treatment with statins is associated with an increased risk of fatal and nonfatal cancers.
We searched the Medline database between January 1966 and December 1999 for randomized, controlled trials of human subjects in which monotherapy with a statin was compared with placebo. No language restrictions were applied. Only trials with a minimum treatment duration of 4 years and a minimum of 1,000 subjects were included. Studies that did not provide information on fatal or nonfatal cancers were excluded. Data on fatal and nonfatal cancers and all-cause mortality were extracted by a single nonblinded reviewer. Overall crude estimates of risk difference were computed by summing the numerators and denominators of trial-specific risk estimates.
Five trials met the inclusion criteria. The estimated differences in absolute risk between treatment and placebo were as follows (negative risks indicate that treatment was safer than placebo): all nonfatal cancers, 0.0% (95% confidence interval [CI]: -0.8% to 0.8%); all fatal cancers, -0.1% (95% CI: -0.7% to 0.4%); all fatal and nonfatal cancers combined, -0.1% (95% CI: -1.0% to 0.7%); and all-cause mortality, -1.5% (95% CI: 2.8% to 0.2%).
This study demonstrates no association between statin use over a 5-year period and the risk of fatal and nonfatal cancers. This conclusion is limited by the relatively short follow-up of the studies analyzed. Similar analyses of data from studies with longer follow-up periods would be valuable.
尽管他汀类药物的短期安全性和耐受性已得到充分证实,但其长期潜在致癌性仍存在争议。本研究的目的是确定长期使用他汀类药物是否会增加致命和非致命癌症的风险。
我们检索了1966年1月至1999年12月的Medline数据库,以查找人类受试者的随机对照试验,其中将他汀类药物单药治疗与安慰剂进行了比较。不设语言限制。仅纳入治疗持续时间至少为4年且受试者至少为1000人的试验。未提供致命或非致命癌症信息的研究被排除。由一位非盲法评审员提取致命和非致命癌症以及全因死亡率的数据。通过汇总特定试验风险估计值的分子和分母来计算总体风险差异的粗略估计值。
五项试验符合纳入标准。治疗组与安慰剂组之间的绝对风险估计差异如下(负风险表明治疗比安慰剂更安全):所有非致命癌症,0.0%(95%置信区间[CI]:-0.8%至0.8%);所有致命癌症,-0.1%(95%CI:-0.7%至0.4%);所有致命和非致命癌症合并,-0.1%(95%CI:-1.0%至0.7%);全因死亡率,-1.5%(95%CI:-2.8%至0.2%)。
本研究表明,5年期间使用他汀类药物与致命和非致命癌症的风险之间无关联。这一结论受到所分析研究相对较短随访期的限制。对随访期更长的研究数据进行类似分析将很有价值。