Rauen Thomas, Wied Stephanie, Fitzner Christina, Eitner Frank, Sommerer Claudia, Zeier Martin, Otte Britta, Panzer Ulf, Budde Klemens, Benck Urs, Mertens Peter R, Kuhlmann Uwe, Witzke Oliver, Gross Oliver, Vielhauer Volker, Mann Johannes F E, Hilgers Ralf-Dieter, Floege Jürgen
Division of Nephrology and Clinical Immunology, RWTH Aachen University, Aachen, Germany.
Department of Medical Statistics, RWTH Aachen University, Aachen, Germany.
Kidney Int. 2020 Oct;98(4):1044-1052. doi: 10.1016/j.kint.2020.04.046. Epub 2020 May 22.
The randomized, controlled STOP-IgAN trial in patients with IgA nephropathy (IgAN) and substantial proteinuria showed no benefit of immunosuppression added on top of supportive care on renal function over three years. As a follow-up we evaluated renal outcomes in patients over a follow-up of up to ten years in terms of serum creatinine, proteinuria, end-stage kidney disease (ESKD), and death. The adapted primary endpoint was the time to first occurrence of a composite of death, ESKD, or a decline of over 40% in the estimated glomerular filtration rate (eGFR) compared to baseline at randomization into STOP-IgAN. Data were analyzed by Cox-regression models. Follow-up data were available for 149 participants, representing 92% of the patients originally randomized. Median follow-up was 7.4 years (inter quartile range 5.7 to 8.3 years). The primary endpoint was reached in 36 of 72 patients randomized to supportive care and 35 of 77 patients randomized to additional immunosuppression (hazard ratio 1.20; 95% confidence interval 0.75 to 1.92). ESKD occurred in 17 of the patients with supportive care and in 20 of the patients with additional immunosuppression. Additionally, the rates of eGFR loss over 40% and annual eGFR loss did not differ between groups. Two patients died with supportive care and three with additional immunosuppression. Thus, within the limitations of a retrospective study, over a follow-up of up to ten years, and using an adapted primary endpoint, we failed to detect differences in key clinical outcomes in IgAN patients randomized to receive added immunosuppression on top of supportive care versus supportive care alone.
在患有IgA肾病(IgAN)且有大量蛋白尿的患者中进行的随机对照STOP-IgAN试验表明,在三年时间里,在支持性治疗基础上加用免疫抑制治疗对肾功能并无益处。作为后续研究,我们对患者进行了长达十年的随访,评估了血清肌酐、蛋白尿、终末期肾病(ESKD)和死亡方面的肾脏转归。调整后的主要终点是与随机分组进入STOP-IgAN时的基线相比,首次出现死亡、ESKD或估计肾小球滤过率(eGFR)下降超过40%的复合事件的时间。数据采用Cox回归模型进行分析。有149名参与者的随访数据可用,占最初随机分组患者的92%。中位随访时间为7.4年(四分位间距为5.7至8.3年)。在随机接受支持性治疗的72名患者中,有36名达到主要终点;在随机接受额外免疫抑制治疗的77名患者中,有35名达到主要终点(风险比1.20;95%置信区间为0.75至1.92)。接受支持性治疗的患者中有17人发生ESKD,接受额外免疫抑制治疗的患者中有20人发生ESKD。此外,两组之间eGFR下降超过40%的发生率和年度eGFR下降率并无差异。接受支持性治疗的患者中有2人死亡,接受额外免疫抑制治疗的患者中有3人死亡。因此,在回顾性研究的局限性范围内,经过长达十年的随访,并使用调整后的主要终点,我们未能检测出随机接受在支持性治疗基础上加用免疫抑制治疗与单纯支持性治疗的IgAN患者在关键临床转归上的差异。