Department of Nephrology and Immunology, UMR 643, CHU de Nantes, Nantes, France.
Department of Nephrology and Immunology, UMR 643, CHU de Nantes, Nantes, France.
Am J Kidney Dis. 2016 Jul;68(1):84-93. doi: 10.1053/j.ajkd.2015.12.034. Epub 2016 Mar 21.
BACKGROUND: Atypical hemolytic uremic syndrome (aHUS) is a rare genetic life-threatening disease of chronic uncontrolled complement activation leading to thrombotic microangiopathy (TMA) and severe end-organ damage. Eculizumab, a terminal complement inhibitor approved for aHUS treatment, was reported to improve hematologic and renal parameters in 2 prior prospective phase 2 studies. This is the largest prospective study of eculizumab in aHUS to date, conducted in an adult population. STUDY DESIGN: Open-label single-arm phase 2 trial. SETTING & PARTICIPANTS: Patients 18 years or older with aHUS (platelet count <150 × 10(3)/μL, hemoglobin ≤ lower limit of normal, lactate dehydrogenase ≥1.5 × upper limit of normal [ULN], and serum creatinine ≥ ULN) were included in this multicenter multinational study. INTERVENTION: Intravenous eculizumab (900mg/wk for 4 weeks, 1,200mg at week 5 and then every 2 weeks) for 26 weeks. OUTCOMES & MEASUREMENTS: Primary end point was complete TMA response within 26 weeks, defined as hematologic normalization (platelet count ≥150 × 10(3)/μL, LDH ≤ ULN), and preservation of kidney function (<25% serum creatinine increase from baseline), confirmed by 2 or more consecutive measurements obtained 4 or more weeks apart. RESULTS: 41 patients were treated; 38 (93%) completed 26 weeks of treatment. 30 (73%) were included during their first TMA manifestation. 30 (73%) had complete TMA response. Platelet counts and estimated glomerular filtration rates increased from baseline (P<0.001). All 35 patients on baseline plasma exchange/plasma infusion discontinued by week 26. Of 24 patients requiring baseline dialysis, 5 recovered kidney function before eculizumab initiation and 15 of the remaining 19 (79%) discontinued dialysis during eculizumab treatment. No patients lost existing transplants. Quality-of-life measures were significantly improved. Two patients developed meningococcal infections; both recovered, and 1 remained on eculizumab treatment. LIMITATIONS: Single-arm open-label design. CONCLUSIONS: Results highlight the benefits of eculizumab in adult patients with aHUS: improvement in hematologic, renal, and quality-of-life parameters; dialysis discontinuation; and transplant protection.
背景:非典型溶血性尿毒症综合征(aHUS)是一种罕见的遗传性危及生命的疾病,其特征为慢性失控的补体激活导致血栓性微血管病(TMA)和严重的终末器官损伤。依库珠单抗是一种已被批准用于治疗 aHUS 的末端补体抑制剂,在之前的两项前瞻性 2 期研究中显示可改善血液学和肾脏参数。这是迄今为止在成人人群中进行的最大规模的依库珠单抗治疗 aHUS 的前瞻性研究。
研究设计:开放标签单臂 2 期试验。
设置和参与者:本多中心多国研究纳入了年龄在 18 岁及以上的 aHUS 患者(血小板计数<150×103/μL,血红蛋白≤正常值下限,乳酸脱氢酶≥1.5×正常值上限[ULN],血清肌酐≥ULN)。
干预措施:静脉内依库珠单抗(4 周每周 900mg,第 5 周 1200mg,然后每 2 周 1200mg)治疗 26 周。
结果:41 例患者接受了治疗;38 例(93%)完成了 26 周的治疗。30 例(73%)在首次 TMA 发作时纳入研究。30 例(73%)获得完全 TMA 反应。血小板计数和估算肾小球滤过率从基线升高(P<0.001)。所有 35 例基线时接受血浆置换/血浆输注的患者在第 26 周时均停止治疗。24 例需要基线透析的患者中,有 5 例在依库珠单抗治疗前恢复了肾功能,而其余 19 例中有 15 例(79%)在依库珠单抗治疗期间停止了透析。没有患者失去现有的移植器官。生活质量测量指标显著改善。有 2 例患者发生脑膜炎球菌感染;均恢复,其中 1 例仍在接受依库珠单抗治疗。
局限性:单臂开放标签设计。
结论:结果强调了依库珠单抗在成人 aHUS 患者中的益处:血液学、肾脏和生活质量参数改善;停止透析;以及保护移植器官。
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