Clinical Implications of Slope of GFR in Clinical Trials of CKD Progression

医学 肾功能 肾脏疾病 肌酐 内科学 临床试验 临床终点 随机对照试验 泌尿科 置信区间 代理终结点
作者
Tom Greene,Willem Collier,Benjamin Haaland,Chong Zhang,Sunil V. Badve,Fernando Caravaca‐Fontán,Lucia Del Vecchio,Jürgen Floege,Thierry Hannedouche,Enyu Imai,Tazeen H. Jafar,Julia B. Lewis,Philip Kam‐Tao Li,Francesco Locatelli,Bart Maes,Brendon L. Neuen,Ronald D. Perrone,Francesco Paolo Schena,Robert D. Toto,Christoph Wanner
出处
期刊:Clinical Journal of The American Society of Nephrology [Lippincott Williams & Wilkins]
卷期号:20 (5): 632-641 被引量:2
标识
DOI:10.2215/cjn.0000000662
摘要

Key Points Acute effects impact the clinical endpoint independently of treatment effects on the chronic slope. Our findings support the 3-year total slope as the primary slope-based outcome in randomized trials. Background Slope of the GFR is considered a validated surrogate endpoint for CKD trials. However, differing short-term and long-term treatment effects on GFR slope can create ambiguities concerning the appropriate period for evaluating slope, in part because current methods cannot separate the distinct contributions of the acute (before 3 months) and chronic (after 3 months) slopes for treatment effects on clinical endpoints (CEs). Methods We estimated treatment effects on the acute and chronic GFR slopes and on the established CE of kidney failure or serum creatinine doubling for 66 randomized treatment comparisons from previous CKD clinical trials. We used a novel Bayesian meta-regression framework to relate treatment effects on the established CE to both the acute and chronic slopes in a single multivariable model to determine the independent contributions of the acute and chronic slopes. Results Treatment effects on both the acute and chronic slopes independently predicted the treatment effect on the established CE with a high median R 2 (95% credible interval) of 0.95 (0.79 to 1.00). For a fixed treatment effect on the chronic slope, each 1 ml/min per 1.73 m 2 greater acute GFR decline for the treatment versus control increased the hazard ratio for the established CE by 11.4% (7.9%–15.0%), against the treatment. The optimal weights for the acute and chronic slopes were consistent with the 3-year total slope defined as the average slope extending from baseline to 3 years. Conclusions Treatment effects on both the acute and chronic GFR slopes are independent determinants of the effects on the established CE, with variation in acute effects accounting for much of the observed variation in treatment effects on the CE across previous trials. Our results establish that acute effects affect the CE independently of treatment effects on the chronic slope and support the 3-year total slope as the primary slope-based outcome in randomized trials.
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