Center for Cardiovascular Disease Prevention, Brigham and Women's Hospital, Harvard Medical School, 900 Commonwealth Avenue, Boston, MA, USA.
Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, 75 Francis Street, Boston, MA, USA.
Eur Heart J. 2018 Oct 7;39(38):3499-3507. doi: 10.1093/eurheartj/ehy310.
Canakinumab, a monoclonal antibody targeting interleukin (IL)-1β, reduces rates of recurrent cardiovascular events without lowering lipids. It is uncertain, however, to what extent these beneficial cardiovascular outcomes are mediated through interleukin-6 (IL-6) signalling, an issue with substantial pathophysiologic consequences and therapeutic implications.
A total of 4833 stable atherosclerosis patients in the Canakinumab Anti-Inflammatory Thrombosis Outcomes Study (CANTOS) had IL-6 levels measured before randomization and after treatment with placebo or one of three doses of canakinumab (50 mg, 150 mg, or 300 mg) given subcutaneously once every 3 months. Participants were followed for up to 5 years (median follow-up 3.7 years). Compared with those allocated to placebo, CANTOS participants receiving canakinumab who achieved on-treatment IL-6 levels below the study median value of 1.65 ng/L experienced a 32% reduction in major adverse cardiovascular events [MACE, multivariable adjusted hazard ratio (HRadj) 0.68, 95% confidence interval (CI) 0.56-0.82; P < 0.0001], a 30% reduction in MACE plus the additional endpoint of hospitalization for unstable angina requiring urgent revascularization (MACE+, HRadj 0.70, 95% CI 0.59-0.84; P < 0.0001), a 52% reduction in cardiovascular mortality (HRadj 0.48, 95% CI 0.34-0.68; P < 0.0001), and a 48% reduction in all-cause mortality (HRadj 0.52, 95% CI 0.40-0.68; P < 0.0001) with prolonged treatment. In contrast, those with on-treatment IL-6 levels equal to or above 1.65 ng/L after taking the first dose of canakinumab had no significant benefit for any of these endpoints. These differential findings based on the magnitude of IL-6 response were seen in analyses alternatively based on tertiles of on-treatment IL-6 levels, and in analyses using a statistical inference approach to estimate the effect of treatment among individuals who would achieve a targeted IL-6 level.
CANTOS provides proof of concept evidence in humans that modulation of the IL-6 signalling pathway, at least with canakinumab, associates with reduced cardiovascular event rates, independent of lipid lowering.
ClinicalTrials.gov NCT01327846.
靶向白细胞介素 (IL)-1β 的单克隆抗体卡那单抗可降低复发性心血管事件的发生率,而不降低血脂。然而,尚不清楚这些有益的心血管结局在多大程度上是通过白细胞介素-6 (IL-6) 信号传导介导的,这是一个具有重要病理生理后果和治疗意义的问题。
共有 4833 例稳定的动脉粥样硬化患者参加了 Canakinumab Anti-Inflammatory Thrombosis Outcomes Study(CANTOS),这些患者在随机分组前和接受安慰剂或卡那单抗(50mg、150mg 或 300mg)皮下注射,每 3 个月一次治疗后测量了 IL-6 水平。参与者的随访时间最长为 5 年(中位随访时间为 3.7 年)。与接受安慰剂的患者相比,接受卡那单抗治疗且治疗期间 IL-6 水平低于研究中位数 1.65ng/L 的 CANTOS 患者,其主要不良心血管事件(MACE,多变量调整后的危险比 [HRadj] 0.68,95%置信区间 [CI] 0.56-0.82;P<0.0001)、MACE 加不稳定型心绞痛需要紧急血运重建的住院治疗(MACE+,HRadj 0.70,95%CI 0.59-0.84;P<0.0001)、心血管死亡率(HRadj 0.48,95%CI 0.34-0.68;P<0.0001)和全因死亡率(HRadj 0.52,95%CI 0.40-0.68;P<0.0001)分别降低了 32%、30%、52%和 48%,且随着治疗时间的延长而降低。相比之下,首次接受卡那单抗治疗后,IL-6 水平等于或高于 1.65ng/L 的患者在这些终点均无显著获益。这些基于 IL-6 反应幅度的差异发现,在基于治疗期间 IL-6 水平三分位数的分析中,以及在使用统计学推断方法估计达到目标 IL-6 水平的个体的治疗效果的分析中均得到证实。
CANTOS 为人类提供了概念验证证据,表明至少通过卡那单抗抑制 IL-6 信号通路与降低心血管事件发生率相关,而与降脂无关。
ClinicalTrials.gov NCT01327846。