Green Lane Cardiovascular Service, Auckland City Hospital, Auckland, New Zealand.
Brigham and Women's Hospital, Heart & Vascular Center, and Harvard Medical School, Boston, Massachusetts.
JACC Cardiovasc Interv. 2015 Mar;8(3):424-433. doi: 10.1016/j.jcin.2014.09.025. Epub 2015 Feb 18.
The aim of this study was to examine the efficacy and bleeding outcomes of cangrelor in patients in the CHAMPION PHOENIX (A Clinical Trial Comparing Cangrelor to Clopidogrel Standard Therapy in Subjects Who Require Percutaneous Coronary Intervention [PCI]) who underwent percutaneous coronary intervention with bivalirudin.
Cangrelor is a potent intravenous P2Y12 inhibitor with rapid onset and offset. In the CHAMPION PHOENIX, cangrelor compared with clopidogrel significantly reduced 48-h ischemic events including stent thrombosis, without increasing major bleeding. Bivalirudin has demonstrated ischemic outcomes similar to those with heparin plus glycoprotein IIb/IIIa inhibition, with reduced bleeding but increased early stent thrombosis.
In the modified intent-to-treat population, 2,059 patients (18.8%) received bivalirudin, with 1,014 patients in the cangrelor treatment arm and 1,045 in the clopidogrel treatment arm.
At 48 h, the primary endpoint of death, myocardial infarction, ischemia-driven revascularization, or stent thrombosis was lower with cangrelor versus clopidogrel (48 [4.7%] vs. 70 [6.7%]; odds ratio [OR]: 0.68, p = 0.047). Death was similar in both arms (2 [0.2%] vs. 2 [0.2%]). Myocardial infarction was reduced by cangrelor (37 [3.6%] vs. 59 [5.6%]; OR: 0.63, p = 0.03), as was death/myocardial infarction (39 [3.8%] vs. 61 [5.8%]; OR: 0.65, p = 0.04). Cangrelor was associated with a nonsignificant trend toward less stent thrombosis (7 [0.7%] vs. 15 [1.4%]; OR: 0.48, p = 0.10), which was evident within 2 h after percutaneous coronary intervention (p = 0.057). GUSTO (Global Use of Strategies to Open Occluded Arteries) severe bleeding was similar in both arms (2 of 1,021 [0.2%] vs. 2 of 1,055 [0.2%]) as were other bleeding definitions and transfusions. Efficacy and safety results were consistent in patients with stable angina, non-ST-segment elevation acute coronary syndrome, and ST-segment elevation myocardial infarction (p for interaction: 0.62 and 0.29).
Cangrelor may offer an attractive benefit risk profile when used in combination with bivalirudin.
本研究旨在评估坎格雷洛在接受经皮冠状动脉介入治疗(PCI)的患者中的疗效和出血结局,这些患者在 CHAMPION PHOENIX(比较需要 PCI 的患者中坎格雷洛与氯吡格雷标准治疗的临床试验)中接受了比伐卢定治疗。
坎格雷洛是一种强效的静脉内 P2Y12 抑制剂,具有快速起效和消除作用。在 CHAMPION PHOENIX 中,坎格雷洛与氯吡格雷相比,显著降低了 48 小时内的缺血事件,包括支架血栓形成,而不增加大出血。比伐卢定显示出与肝素加糖蛋白 IIb/IIIa 抑制相似的缺血结局,出血减少,但早期支架血栓形成增加。
在改良意向治疗人群中,2059 例患者(18.8%)接受了比伐卢定治疗,其中 1014 例患者接受了坎格雷洛治疗,1045 例患者接受了氯吡格雷治疗。
在 48 小时时,坎格雷洛组与氯吡格雷组的主要终点(死亡、心肌梗死、缺血驱动的血运重建或支架血栓形成)较低(48 [4.7%] vs. 70 [6.7%];比值比[OR]:0.68,p = 0.047)。两组的死亡率相似(2 [0.2%] vs. 2 [0.2%])。心肌梗死发生率降低(37 [3.6%] vs. 59 [5.6%];OR:0.63,p = 0.03),死亡/心肌梗死发生率降低(39 [3.8%] vs. 61 [5.8%];OR:0.65,p = 0.04)。支架血栓形成发生率有降低趋势,但无统计学意义(7 [0.7%] vs. 15 [1.4%];OR:0.48,p = 0.10),这在 PCI 后 2 小时内即可观察到(p = 0.057)。GUSTO(全球使用策略以开放闭塞动脉)严重出血在两组间相似(1021 例中有 2 例[0.2%] vs. 1055 例中有 2 例[0.2%]),其他出血定义和输血也是如此。在稳定性心绞痛、非 ST 段抬高型急性冠状动脉综合征和 ST 段抬高型心肌梗死患者中,疗效和安全性结果一致(p 交互作用:0.62 和 0.29)。
当与比伐卢定联合使用时,坎格雷洛可能具有有吸引力的风险获益特征。