Department of Cardiology, Lund University, Lund, Sweden.
J Am Coll Cardiol. 2013 Aug 13;62(7):577-83. doi: 10.1016/j.jacc.2013.05.023. Epub 2013 Jun 7.
This study assessed pharmacodynamic (PD) response to the reduced prasugrel maintenance dose of 5 mg in very elderly (VE) patients (≥75 years of age).
In the TRITON-TIMI 38 (TRial to Assess Improvement in Therapeutic Outcomes by Optimizing Platelet InhibitioN with Prasugrel-Thrombolysis In Myocardial Infarction 38) study prasugrel 10 mg reduced ischemic events versus clopidogrel 75 mg, but increased bleeding in VE patients.
We examined PD and active metabolite pharmacokinetics (PKs) with prasugrel 5 and 10 mg and clopidogrel 75 mg in a 3-period (12 days each) blinded, crossover study in VE (n = 73; mean: 79 ± 3 years of age) or (n = 82) nonelderly (NE) (≥45 to <65 years of age; mean: 56 ± 5 years of age) stable coronary artery disease (CAD) patients receiving background aspirin. Assays included light transmission aggregometry (LTA), VerifyNow P2Y12 (VN-P2Y12), and vasodilator-associated stimulated phosphoprotein (VASP). The primary comparison was noninferiority of maximum platelet aggregation (MPA) comparing the median for prasugrel 5 mg in VE versus the 75th percentile for prasugrel 10 mg in NE, using a pre-specified 1-sided 97.5% confidence interval for the difference <15%.
Prasugrel 5 mg in VE met the primary PD noninferiority criterion versus prasugrel 10 mg in NE. For prasugrel 5 mg, MPA was significantly lower (57 ± 14%) than clopidogrel (63 ± 14%; p < 0.001) in VE but higher than prasugrel 10 mg in NE (46 ± 12%; p < 0.001). PD response by LTA, VN-P2Y12, and VASP during all treatments appeared similar between age cohorts. Prasugrel 5 mg resulted in fewer VE poor responders than clopidogrel. Rates of mild bleeding were higher with prasugrel 10 mg but similar for prasugrel 5 mg versus clopidogrel 75 mg.
In aspirin-treated stable CAD patients, prasugrel 5 mg in VE attenuated platelet inhibition while meeting pre-specified noninferiority criterion versus prasugrel 10 mg in NE, with significantly better PD response and fewer poor responders compared to clopidogrel 75 mg in VE. (Comparison of Prasugrel and Clopidogrel in Very Elderly and Non-Elderly Patients With Stable Coronary Artery Disease [GENERATIONS]; NCT01107912).
本研究评估了非常老年(VE)患者(≥75 岁)中普拉格雷维持剂量降低至 5mg 的药效学(PD)反应。
TRITON-TIMI 38(评估通过优化血小板抑制作用改善治疗结果的试验,普拉格雷-心肌梗死 38 溶栓)研究表明,普拉格雷 10mg 降低了缺血事件,而氯吡格雷 75mg 增加了 VE 患者的出血。
我们在 VE(n=73;平均年龄:79±3 岁)或(n=82)非老年(NE)(≥45 至<65 岁;平均年龄:56±5 岁)稳定型冠心病(CAD)患者中进行了一项 3 期(每期 12 天)、双盲、交叉研究,评估了普拉格雷 5mg 和 10mg 以及氯吡格雷 75mg 的 PD 和活性代谢物药代动力学(PKs)。研究包括光传输聚集测定法(LTA)、VerifyNow P2Y12(VN-P2Y12)和血管扩张剂相关的刺激磷酸蛋白(VASP)。主要比较是 VE 中普拉格雷 5mg 的最大血小板聚集(MPA)的中位数与 NE 中普拉格雷 10mg 的第 75 百分位数之间的非劣效性,使用预先指定的 1 侧 97.5%置信区间,差值<15%。
VE 中普拉格雷 5mg 符合与 NE 中普拉格雷 10mg 相比的主要 PD 非劣效性标准。对于普拉格雷 5mg,VE 中的 MPA 明显低于氯吡格雷(63±14%;p<0.001),但高于 NE 中的普拉格雷 10mg(46±12%;p<0.001)。在所有治疗中,通过 LTA、VN-P2Y12 和 VASP 进行的 PD 反应在年龄组之间似乎相似。普拉格雷 5mg 在 VE 中的不良反应者比氯吡格雷少。普拉格雷 10mg 轻度出血率较高,但与普拉格雷 5mg 相比,与氯吡格雷 75mg 相似。
在接受阿司匹林治疗的稳定型 CAD 患者中,VE 中普拉格雷 5mg 减轻了血小板抑制作用,同时符合与 NE 中普拉格雷 10mg 相比的非劣效性标准,与 VE 中的氯吡格雷 75mg 相比,PD 反应更好,不良反应者更少。(普拉格雷与氯吡格雷在稳定型冠状动脉疾病的非常老年和非老年患者中的比较[世代];NCT01107912)。