Bouts Antonia, Veltkamp Floor, Tönshoff Burkhard, Vivarelli Marina
Department of Pediatric Nephrology, Emma Children's Hospital, AMC, Amsterdam, the Netherlands.
Department of Pediatrics I, University Children's Hospital Heidelberg, Heidelberg, Germany.
Pediatr Transplant. 2019 May;23(3):e13385. doi: 10.1111/petr.13385. Epub 2019 Mar 1.
Primary FSGS is an important cause of ESRD in children. FSGS recurrence after kidney transplantation is associated with early graft loss. No guidelines for treatment of FSGS recurrence exist. We conducted a survey to gain insight into variation of treatment between centers.
A survey was sent to all members of the ESPN on behalf of the "Renal Transplantation" and "Idiopathic Nephrotic Syndrome" working groups.
Fifty-nine nephrologists from 31 countries responded, reporting 807 FSGS patients, with 241 (30%) FSGS recurrences after transplantation. Recurrence varied from 0% to 100% between respondents. Native nephrectomy before or during transplantation was performed, respectively, always (37%), never (39%), or on clinical indication (17%). Half of the respondents started preventive treatment before transplantation, using PF (n = 10); R (n = 4); PF or IA, plus R (n = 9); cyclosporine (n = 2); or unknown (n = 4). Immunosuppressive therapy for patients without known mutations consisted of a combination of steroids, tacrolimus/cyclosporine, and MMF, with or without IL-2R-blockade in, respectively, 61% and 86% of the respondents. Sixty-three percent applied a similar regimen to patients with known mutations. FSGS recurrence was treated with PF or IA, plus R by 66% of respondents; 54% observed no response. Complete remission in >50% of patients was reported by 41% of the respondents.
FSGS recurrence after transplantation is common, but varies greatly between centers. We found great variability in preventive and therapeutic treatment regimens. Future research should focus on predisposing factors, including biopsy findings and genetic mutations, and standardized treatment.
原发性局灶节段性肾小球硬化(FSGS)是儿童终末期肾病(ESRD)的重要病因。肾移植后FSGS复发与移植肾早期丢失相关。目前尚无FSGS复发的治疗指南。我们开展了一项调查,以深入了解各中心治疗方法的差异。
代表“肾移植”和“特发性肾病综合征”工作组,向欧洲小儿肾病学会(ESPN)的所有成员发送了一份调查问卷。
来自31个国家的59名肾病专家进行了回复,报告了807例FSGS患者,其中241例(30%)移植后出现FSGS复发。各回复者报告的复发率从0%至100%不等。移植前或移植期间进行患肾切除术的情况分别为:总是进行(37%)、从不进行(39%)或根据临床指征进行(17%)。一半的回复者在移植前开始预防性治疗,使用的药物为:蛋白A(PF,n = 10);利妥昔单抗(R,n = 4);PF或免疫吸附(IA)加R(n = 9);环孢素(n = 2);或情况不明(n = 4)。对于无已知突变的患者,免疫抑制治疗方案包括类固醇、他克莫司/环孢素和霉酚酸酯(MMF)联合使用,分别有61%和86%的回复者使用或未使用白细胞介素-2受体阻滞剂(IL-2R-blockade)。63%的回复者对有已知突变的患者采用类似方案。66%的回复者使用PF或IA加R治疗FSGS复发;54%的回复者观察到无反应。41%的回复者报告超过50%的患者完全缓解。
移植后FSGS复发很常见,但各中心差异很大。我们发现预防性和治疗性治疗方案存在很大差异。未来的研究应关注易感因素,包括活检结果和基因突变,以及标准化治疗。