Clinical Trial Service Unit, University of Oxford, Oxford, United Kingdom
Thrombolysis in Myocardial Infarction Study Group, Brigham and Women’s Hospital
N Engl J Med. 2017 Sep 28;377(13):1217-1227. doi: 10.1056/NEJMoa1706444. Epub 2017 Aug 28.
Patients with atherosclerotic vascular disease remain at high risk for cardiovascular events despite effective statin-based treatment of low-density lipoprotein (LDL) cholesterol levels. The inhibition of cholesteryl ester transfer protein (CETP) by anacetrapib reduces LDL cholesterol levels and increases high-density lipoprotein (HDL) cholesterol levels. However, trials of other CETP inhibitors have shown neutral or adverse effects on cardiovascular outcomes.
We conducted a randomized, double-blind, placebo-controlled trial involving 30,449 adults with atherosclerotic vascular disease who were receiving intensive atorvastatin therapy and who had a mean LDL cholesterol level of 61 mg per deciliter (1.58 mmol per liter), a mean non-HDL cholesterol level of 92 mg per deciliter (2.38 mmol per liter), and a mean HDL cholesterol level of 40 mg per deciliter (1.03 mmol per liter). The patients were assigned to receive either 100 mg of anacetrapib once daily (15,225 patients) or matching placebo (15,224 patients). The primary outcome was the first major coronary event, a composite of coronary death, myocardial infarction, or coronary revascularization.
During the median follow-up period of 4.1 years, the primary outcome occurred in significantly fewer patients in the anacetrapib group than in the placebo group (1640 of 15,225 patients [10.8%] vs. 1803 of 15,224 patients [11.8%]; rate ratio, 0.91; 95% confidence interval, 0.85 to 0.97; P=0.004). The relative difference in risk was similar across multiple prespecified subgroups. At the trial midpoint, the mean level of HDL cholesterol was higher by 43 mg per deciliter (1.12 mmol per liter) in the anacetrapib group than in the placebo group (a relative difference of 104%), and the mean level of non-HDL cholesterol was lower by 17 mg per deciliter (0.44 mmol per liter), a relative difference of -18%. There were no significant between-group differences in the risk of death, cancer, or other serious adverse events.
Among patients with atherosclerotic vascular disease who were receiving intensive statin therapy, the use of anacetrapib resulted in a lower incidence of major coronary events than the use of placebo. (Funded by Merck and others; Current Controlled Trials number, ISRCTN48678192 ; ClinicalTrials.gov number, NCT01252953 ; and EudraCT number, 2010-023467-18 .).
尽管通过他汀类药物有效治疗了低密度脂蛋白(LDL)胆固醇水平,患有动脉粥样硬化性血管疾病的患者仍存在较高的心血管事件风险。抑制胆固醇酯转移蛋白(CETP)的阿昔单抗可降低 LDL 胆固醇水平并增加高密度脂蛋白(HDL)胆固醇水平。然而,其他 CETP 抑制剂的临床试验显示对心血管结局呈中性或不利影响。
我们进行了一项随机、双盲、安慰剂对照试验,纳入了 30449 名患有动脉粥样硬化性血管疾病的成年人,他们正在接受强化阿托伐他汀治疗,且 LDL 胆固醇水平平均为 61mg/分升(1.58mmol/L),非高密度脂蛋白胆固醇水平平均为 92mg/分升(2.38mmol/L),高密度脂蛋白胆固醇水平平均为 40mg/分升(1.03mmol/L)。患者被随机分配接受每天一次 100mg 阿昔单抗(15225 例患者)或匹配安慰剂(15224 例患者)治疗。主要终点是首次主要冠状动脉事件,即包括冠状动脉死亡、心肌梗死或冠状动脉血运重建的复合终点。
在中位随访 4.1 年期间,阿昔单抗组的主要终点事件发生率明显低于安慰剂组(15225 例患者中有 1640 例[10.8%] vs. 15224 例患者中有 1803 例[11.8%];率比为 0.91;95%置信区间为 0.85 至 0.97;P=0.004)。多个预先指定的亚组中,风险的相对差异相似。在试验中点,阿昔单抗组的 HDL 胆固醇平均水平升高 43mg/分升(1.12mmol/L),而安慰剂组升高 112%(相对差异为 104%),非高密度脂蛋白胆固醇平均水平降低 17mg/分升(0.44mmol/L),相对差异为-18%。两组间死亡率、癌症或其他严重不良事件的风险无显著差异。
在接受强化他汀类药物治疗的动脉粥样硬化性血管疾病患者中,与安慰剂相比,使用阿昔单抗可降低主要冠状动脉事件的发生率。(由默克公司及其它公司资助;当前对照试验编号,ISRCTN48678192;临床试验编号,NCT01252953;和 EudraCT 编号,2010-023467-18)。