Department of Nephrology and Immunology, ITUN and INSERM UMR S-1064, CHU de Nantes, Nantes, France.
Department of Nephrology, CHU de Bordeaux, Bordeaux, France.
Am J Kidney Dis. 2014 Jan;63(1):40-8. doi: 10.1053/j.ajkd.2013.07.011. Epub 2013 Sep 8.
Atypical hemolytic uremic syndrome (aHUS) is a devastating form of renal thrombotic microangiopathy. Despite plasma exchange, the standard treatment of aHUS for decades, the renal prognosis for patients with aHUS has remained poor. We assessed the off-trial use of eculizumab in adult patients with aHUS affecting the native kidneys.
A retrospective study was conducted. aHUS was defined as the presence of 3 or more of the following: acute kidney injury (serum creatinine >1.4 mg/dL [120 μmol/L]), mechanical hemolytic anemia, thrombocytopenia, and the presence of thrombotic microangiopathy features in a kidney biopsy specimen. Patients who had received 4 or more weekly 900-mg infusions of eculizumab were included.
SETTING & PARTICIPANTS: 19 patients were identified through a query sent to all French nephrology centers.
OUTCOMES & MEASUREMENTS: Evolution of kidney function, hemolysis, and thrombocytopenia after the initiation of eculizumab therapy.
All patients had acute kidney injury (serum creatinine range, 2.2-17.0 mg/dL) and 12 required hemodialysis. Thirteen patients carried a mutation in 1 complement gene and 1 had anti-factor H antibodies. For first-line therapy, 16 patients underwent plasma exchange and 3 patients received eculizumab. Median time between aHUS onset and eculizumab therapy initiation was 6 (range, 1-60) days and median time to platelet count normalization after eculizumab therapy initiation was 6 (range, 2-42) days. At the 3-month follow-up, 4 patients still required dialysis, 8 had non-dialysis-dependent chronic kidney disease, and 7 had normalized kidney function. At last follow-up (range, 4-22 months), 3 patients remained dialysis dependent, 7 had non-dialysis-dependent chronic kidney disease (estimated glomerular filtration rate, 17-55 mL/min/1.73 m(2)), and 9 had normal kidney function. Risks of reaching end-stage renal disease within 3 months and 1 year of aHUS onset were reduced by half in eculizumab-treated patients compared with recent historical controls.
Retrospective study and use of historical controls.
Our data indicate that eculizumab improves kidney disease outcome in patients with aHUS.
非典型溶血性尿毒症综合征(aHUS)是一种严重的肾血栓性微血管病。尽管几十年来一直采用血浆置换作为 aHUS 的标准治疗方法,但 aHUS 患者的肾脏预后仍然较差。我们评估了在不进行临床试验的情况下,使用依库珠单抗治疗影响固有肾脏的成人 aHUS 患者的效果。
进行了一项回顾性研究。aHUS 的定义为存在以下 3 种或以上表现:急性肾损伤(血清肌酐>1.4mg/dL[120μmol/L])、机械性溶血性贫血、血小板减少和肾活检标本中存在血栓性微血管病特征。纳入了接受 4 次或以上每周 900mg 依库珠单抗输注的患者。
通过向所有法国肾病中心发送查询,确定了 19 名患者。
所有患者均有急性肾损伤(血清肌酐范围 2.2-17.0mg/dL),12 名患者需要血液透析。13 名患者携带 1 种补体基因的突变,1 名患者携带抗因子 H 抗体。一线治疗中,16 名患者接受血浆置换,3 名患者接受依库珠单抗治疗。aHUS 发病与依库珠单抗治疗开始之间的中位时间为 6(范围 1-60)天,依库珠单抗治疗开始后血小板计数恢复正常的中位时间为 6(范围 2-42)天。在 3 个月的随访时,4 名患者仍需要透析,8 名患者患有非透析依赖的慢性肾脏病,7 名患者肾功能正常。最后一次随访(范围 4-22 个月)时,3 名患者仍依赖透析,7 名患者患有非透析依赖的慢性肾脏病(估计肾小球滤过率 17-55ml/min/1.73m²),9 名患者肾功能正常。与近期历史对照相比,依库珠单抗治疗患者在 3 个月和 1 年内达到终末期肾脏疾病的风险降低了一半。
回顾性研究和使用历史对照。
我们的数据表明,依库珠单抗改善了 aHUS 患者的肾脏疾病预后。