Reata Pharmaceuticals, Irving, Texas, USA.
University of Chicago Medicine, Chicago, Illinois, USA.
Am J Nephrol. 2018;47(1):40-47. doi: 10.1159/000486398. Epub 2018 Jan 18.
Increases in measured inulin clearance, measured creatinine clearance, and estimated glomerular filtration rate (eGFR) have been observed with bardoxolone methyl in 7 studies enrolling approximately 2,600 patients with type 2 diabetes (T2D) and chronic kidney disease (CKD). The largest of these studies was Bardoxolone Methyl Evaluation in Patients with Chronic Kidney Disease and Type 2 Diabetes (BEACON), a multinational, randomized, double-blind, placebo-controlled phase 3 trial which enrolled patients with T2D and CKD stage 4. The BEACON trial was terminated after preliminary analyses showed that patients randomized to bardoxolone methyl experienced significantly higher rates of heart failure events. We performed post-hoc analyses to characterize changes in kidney function induced by bardoxolone methyl.
Patients in -BEACON (n = 2,185) were randomized 1: 1 to receive once-daily bardoxolone methyl (20 mg) or placebo. We compared the effects of bardoxolone methyl and placebo on a post-hoc composite renal endpoint consisting of ≥30% decline from baseline in eGFR, eGFR <15 mL/min/1.73 m2, and end-stage renal disease (ESRD) events (provision of dialysis or kidney transplantation).
Consistent with prior studies, patients randomized to bardoxolone methyl experienced mean increases in eGFR that were sustained through study week 48. Moreover, increases in eGFR from baseline were sustained 4 weeks after cessation of treatment. Patients randomized to bardoxolone methyl were significantly less likely to experience the composite renal endpoint (hazards ratio 0.48 [95% CI 0.36-0.64]; p < 0.0001).
Bardoxolone methyl preserves kidney function and may delay the onset of ESRD in patients with T2D and stage 4 CKD.
在纳入约 2600 例 2 型糖尿病(T2D)和慢性肾脏病(CKD)患者的 7 项研究中,观察到波达莫司汀治疗后可使菊粉清除率、肌酐清除率和估计肾小球滤过率(eGFR)升高。其中最大的研究是波达莫司汀治疗慢性肾脏病和 2 型糖尿病患者的评估(BEACON),这是一项多中心、随机、双盲、安慰剂对照的 3 期临床试验,纳入了 T2D 和 CKD 4 期患者。初步分析显示,接受波达莫司汀治疗的患者心力衰竭事件发生率显著升高,因此 BEACON 试验提前终止。我们进行了事后分析以明确波达莫司汀引起的肾功能变化。
BEACON 试验(n=2185)中患者按 1:1 随机分为每日一次波达莫司汀(20mg)或安慰剂组。我们比较了波达莫司汀和安慰剂对事后复合肾脏终点的影响,该终点包括 eGFR 较基线下降≥30%、eGFR <15mL/min/1.73m2 和终末期肾病(ESRD)事件(透析或肾移植)。
与既往研究一致,接受波达莫司汀治疗的患者 eGFR 呈持续升高趋势,且在研究第 48 周时仍保持升高。此外,停药后 4 周时 eGFR 仍持续升高。与安慰剂组相比,波达莫司汀组患者发生复合肾脏终点事件的风险显著降低(风险比 0.48[95%CI 0.36-0.64];p<0.0001)。
波达莫司汀可维持肾功能并可能延缓 T2D 和 CKD 4 期患者发生 ESRD。