Wofsy David, Hillson Jan L, Diamond Betty
Arthritis/ Immunology Unit (111R), San Francisco VA Medical Center, 4150 Clement Street, San Francisco, CA 94121, USA.
Arthritis Rheum. 2013 Jun;65(6):1586-91. doi: 10.1002/art.37940.
Clinical trials of therapies for lupus nephritis have used many different primary outcome measures, ranging from complete response to time to end-stage renal disease. The objective of this study was to compare several possible outcome measures, using data from a large, multicenter trial of abatacept in lupus nephritis, to gain insight into which outcome measure, if any, was best able to discern differences among treatment groups.
Study patients received either abatacept or placebo, on a background of mycophenolate mofetil and glucocorticoids. Using data from this trial, the following primary outcome measures at 24 and 52 weeks were compared: complete response rate, major clinical response rate, total response rate (complete plus partial response), improvement in proteinuria, improvement in estimated glomerular filtration rate, and frequency of treatment failure. Time to complete response was also evaluated.
Complete response rate, major clinical response rate, and time to complete response were the measures that best discriminated between the abatacept groups and placebo, and the sensitivities of these 3 measures were comparable. For these measures, sample sizes of 50 patients would have been sufficient to demonstrate a statistically significant difference between treatment and control at 52 weeks. Each of the other measures also discriminated between treatment and control, but much larger group sizes would have been required to determine statistical significance.
The choice of primary outcome measure can substantially influence the ability to detect therapeutic benefit in lupus nephritis trials. This study suggests that complete response rate, major clinical response rate at 52 weeks, and time to complete response may be the most sensitive outcome measures for detecting differences among therapeutic regimens.
狼疮性肾炎治疗的临床试验使用了许多不同的主要结局指标,从完全缓解到终末期肾病时间不等。本研究的目的是利用一项关于阿巴西普治疗狼疮性肾炎的大型多中心试验的数据,比较几种可能的结局指标,以深入了解哪种结局指标(如果有的话)最能辨别治疗组之间的差异。
研究患者在霉酚酸酯和糖皮质激素的基础上接受阿巴西普或安慰剂治疗。利用该试验的数据,比较了24周和52周时以下主要结局指标:完全缓解率、主要临床缓解率、总缓解率(完全缓解加部分缓解)、蛋白尿改善情况、估计肾小球滤过率改善情况以及治疗失败频率。还评估了达到完全缓解的时间。
完全缓解率、主要临床缓解率和达到完全缓解的时间是最能区分阿巴西普组和安慰剂组的指标,这3项指标的敏感性相当。对于这些指标,50例患者的样本量足以在52周时证明治疗组和对照组之间存在统计学显著差异。其他各项指标也能区分治疗组和对照组,但需要大得多的样本量才能确定统计学显著性。
主要结局指标的选择可极大影响狼疮性肾炎试验中检测治疗益处的能力。本研究表明,完全缓解率、52周时的主要临床缓解率以及达到完全缓解的时间可能是检测不同治疗方案间差异最敏感的结局指标。