Department Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
American Society of Hypertension Comprehensive Hypertension Center, University of Chicago Medicine and Biological Sciences, Chicago, Illinois, USA.
Clin Pharmacol Ther. 2021 Jun;109(6):1631-1638. doi: 10.1002/cpt.2143. Epub 2021 Jan 5.
Atrasentan, an endothelin receptor antagonist, showed clinically significant albuminuria reduction with minimal signs of fluid retention in phase II trials. We evaluated whether plasma exposure was associated with long-term outcomes for kidney protection and heart failure in the phase III SONAR trial (n = 3668) in type 2 diabetics with chronic kidney disease. A population pharmacokinetic model was used to estimate plasma exposure of atrasentan 0.75 mg/day. Parametric time-to-event models were used to quantify the association between plasma exposure and long-term outcomes. Mean atrasentan plasma exposure was 41.4 ng.h/mL (2.5th to 97.5th P: 14.2 to 139.9). Compared with placebo, a mean atrasentan exposure translated in a hazard ratio of 0.76 (95% confidence interval (CI): 0.28-0.85) for kidney events and 1.13 (95% CI: 1.03-2.20) for heart failure events. At the mean atrasentan exposure, the kidney protective effect was larger than the increase in heart failure supporting the atrasentan 0.75 mg/day dose in this population.
阿曲生坦是一种内皮素受体拮抗剂,在 II 期临床试验中表现出具有临床意义的白蛋白尿减少,且很少有液体潴留的迹象。我们评估了在 2 型糖尿病合并慢性肾病患者的 III 期 SONAR 试验(n=3668)中,血浆暴露是否与肾脏保护和心力衰竭的长期结局相关。采用群体药代动力学模型来估计阿曲生坦 0.75mg/天的血浆暴露。采用参数时间事件模型来量化血浆暴露与长期结局之间的关联。阿曲生坦的平均血浆暴露为 41.4ng.h/mL(2.5%至 97.5%:14.2 至 139.9)。与安慰剂相比,阿曲生坦的平均暴露转化为肾脏事件的风险比为 0.76(95%置信区间:0.28-0.85),心力衰竭事件的风险比为 1.13(95%置信区间:1.03-2.20)。在阿曲生坦的平均暴露水平下,肾脏保护作用大于心力衰竭的增加,支持该人群中阿曲生坦 0.75mg/天的剂量。