Department of Cardiology, Nephrology, and Intensive Care Medicine, Rhein-Maas Klinikum, Mauerfeldchen 25, 52146, Würselen, Germany.
Salford Royal NHS Foundation Trust, Salford, UK.
J Nephrol. 2019 Oct;32(5):811-821. doi: 10.1007/s40620-019-00631-0. Epub 2019 Aug 10.
Calciphylaxis in end-stage renal disease is characterized by painful necrotic skin ulcers and high mortality. There are no approved therapies. SNF472, an intravenous formulation of myo-inositol hexaphosphate, inhibits the formation and growth of hydroxyapatite crystals, the final common pathway in the pathogenesis of vascular calcification.
In this open-label, single-arm study, calciphylaxis patients on thrice-weekly hemodialysis and standard care, received intravenous SNF472 3 times per week for 12 weeks. The primary endpoint was wound healing assessed using the quantitative Bates-Jensen Wound Assessment Tool (BWAT). Pain visual analog scale (VAS), quality of life (wound-QoL), and qualitative wound image review were secondary endpoints. Quantitative changes from baseline were analyzed by paired t-tests using multiple imputation to account for missing observations.
Fourteen patients received SNF472. Improvements from baseline to week 12 were observed for mean BWAT score (- 8.1; P < 0.001), pain VAS (- 23.6 mm; P = 0.015) and wound-QoL global score (- 0.90; P = 0.003). Of the 9 patients with ulcerated lesions at baseline who completed treatment, wound image review showed improvement for 7. SNF472 was well tolerated with no serious treatment-related adverse events. The most common adverse events were infections which occur frequently in patients on hemodialysis. None of these were considered as treatment-related.
SNF472 was well-tolerated and improvements from baseline to week 12 in wound healing, pain, and quality of life were observed. A randomized, double-blind, placebo-controlled trial is planned to evaluate SNF472 in patients with calciphylaxis.
终末期肾病患者的钙化防御表现为疼痛性坏死性皮肤溃疡和高死亡率。目前尚无批准的治疗方法。SNF472 是肌醇六磷酸的静脉制剂,可抑制羟基磷灰石晶体的形成和生长,这是血管钙化发病机制的最终共同途径。
在这项开放标签、单臂研究中,接受每周三次血液透析和标准治疗的钙化防御患者,每周接受静脉注射 SNF472 3 次,共 12 周。主要终点是使用定量 Bates-Jensen 伤口评估工具(BWAT)评估伤口愈合。次要终点包括疼痛视觉模拟量表(VAS)、生活质量(伤口-QoL)和定性伤口图像复查。采用配对 t 检验分析从基线到第 12 周的定量变化,并采用多重插补法处理缺失观察值。
14 名患者接受了 SNF472 治疗。与基线相比,BWAT 评分(-8.1;P<0.001)、疼痛 VAS(-23.6mm;P=0.015)和伤口-QoL 总评分(-0.90;P=0.003)均有改善。在基线时有溃疡性病变的 9 名患者中,有 7 名患者的伤口图像复查显示有所改善。SNF472 耐受性良好,无严重与治疗相关的不良事件。最常见的不良事件是血液透析患者经常发生的感染,这些不良事件均不认为与治疗有关。
SNF472 耐受性良好,与基线相比,在第 12 周时伤口愈合、疼痛和生活质量均有改善。计划进行一项随机、双盲、安慰剂对照试验,以评估 SNF472 在钙化防御患者中的疗效。