Department for Specialised Paediatrics, Oslo University Hospital, Oslo, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Pediatr Nephrol. 2023 Nov;38(11):3671-3679. doi: 10.1007/s00467-023-06005-w. Epub 2023 May 23.
Nephropathic cystinosis is a rare lysosomal storage disorder in which accumulation of cystine and formation of crystals particularly impair kidney function and gradually lead to multi-organ dysfunction. Lifelong therapy with the aminothiol cysteamine can delay the development of kidney failure and the need for transplant. The purpose of our long-term study was to explore the effects of transitioning from immediate release (IR) to extended release (ER) formulation in Norwegian patients in routine clinical care.
We retrospectively analysed data on efficacy and safety in 10 paediatric and adult patients. Data were obtained from up to 6 years before and 6 years after transitioning from IR- to ER-cysteamine.
Mean white blood cell (WBC) cystine levels remained comparable between the different treatment periods (1.19 versus 1.38 nmol hemicystine/mg protein) although most patients under ER-cysteamine underwent dose reductions. For the non-transplanted patients, the mean estimated glomerular filtration rate (eGFR) change/year was more pronounced during ER-treatment (- 3.39 versus - 6.80 ml/min/1.73 m/year) possibly influenced by individual events, such as tubulointerstitial nephritis and colitis. Growth measured by Z-height score tended to develop positively. Four of seven patients reported improvement of halitosis, one reported unchanged and two reported worsened symptoms. Most adverse drug reactions (ADRs) were of mild severity. One patient developed two serious ADRs and switched back to IR-formulation.
The results from this long-term retrospective study indicate that switching from IR- to ER-cysteamine was feasible and well tolerated under routine clinical practice. ER-cysteamine allowed satisfactory disease control over the long period considered. A higher resolution version of the Graphical abstract is available as Supplementary information.
遗传性胱氨酸贮积症是一种罕见的溶酶体贮积病,其中胱氨酸的积累和晶体的形成特别损害肾功能,并逐渐导致多器官功能障碍。终身用氨硫醇半胱氨酸进行治疗可以延缓肾衰竭的发展和移植的需要。我们进行这项长期研究的目的是在常规临床护理中探索挪威患者从普通释放(IR)到延长释放(ER)制剂转换的效果。
我们回顾性地分析了 10 名儿科和成年患者的疗效和安全性数据。数据来自于从 IR-半胱氨酸胺转换为 ER-半胱氨酸胺之前的 6 年和之后的 6 年。
虽然大多数接受 ER-半胱氨酸胺治疗的患者进行了剂量减少,但白细胞(WBC)半胱氨酸水平的平均值在不同治疗期间保持相似(1.19 与 1.38 nmol 血红素半胱氨酸/毫克蛋白)。对于未接受移植的患者,ER 治疗时的平均估计肾小球滤过率(eGFR)变化/年更为明显(-3.39 与-6.80 ml/min/1.73 m/年),这可能受到个体事件的影响,如肾小管间质性肾炎和结肠炎。通过 Z 身高评分测量的生长趋势呈阳性。七名患者中有四名报告口臭改善,一名报告无变化,两名报告症状恶化。大多数药物不良反应(ADR)为轻度。一名患者发生了两种严重的 ADR,并重新换用 IR 制剂。
这项长期回顾性研究的结果表明,在常规临床实践中,从 IR-半胱氨酸胺转换为 ER-半胱氨酸胺是可行的,并且耐受性良好。在考虑的较长时间内,ER-半胱氨酸胺可实现令人满意的疾病控制。可提供图形摘要的更高分辨率版本作为补充信息。