Robinson Cal H, Aman Nowrin, Banh Tonny, Brooke Josefina, Chanchlani Rahul, Dhillon Vaneet, Langlois Valerie, Levin Leo, Licht Christoph, McKay Ashlene, Noone Damien, Parikh Alisha, Pearl Rachel, Radhakrishnan Seetha, Rowley Veronique, Teoh Chia Wei, Vasilevska-Ristovska Jovanka H, Parekh Rulan S
Division of Nephrology, The Hospital for Sick Children, Toronto, ON, Canada.
Department of Paediatrics, The University of Toronto, Toronto, ON, Canada.
Pediatr Nephrol. 2025 May;40(5):1625-1634. doi: 10.1007/s00467-024-06605-0. Epub 2024 Nov 22.
Steroid-sparing immunosuppression is used in 50% of children with nephrotic syndrome, to prevent relapses and steroid-related toxicity. However, rates and predictors of prolonged remission after cyclophosphamide and tacrolimus are uncertain.
Retrospective analysis of children (1-18 years) enrolled in a longitudinal cohort. We included children diagnosed with steroid-sensitive nephrotic syndrome between 1996-2019 from Toronto, Canada. The exposure was cyclophosphamide or tacrolimus initiation. The primary outcome was prolonged remission (no further relapse or steroid-sparing immunosuppression). We evaluated predictors of prolonged remission and calcineurin inhibitor nephrotoxicity by logistic regression.
Of 578 children with steroid-sensitive nephrotic syndrome, 252 received cyclophosphamide and 120 received tacrolimus. Over median 5.4-year (IQR 2.4-9.1) follow-up, prolonged remission occurred in 72 (28.6%) after cyclophosphamide and 17 (14.2%) after tacrolimus. Relapse frequency decreased after initiation of either medication. Lower prior relapse rate, more recent treatment era, and female sex were predictive of prolonged remission after cyclophosphamide treatment. Use of tacrolimus as the first steroid-sparing medication was the only factor predictive of calcineurin inhibitor nephrotoxicity.
Less than one-third of children achieve prolonged remission after initiating cyclophosphamide or tacrolimus, although both reduce short-term relapse rates. Few factors predict prolonged remission after cyclophosphamide or tacrolimus use, or calcineurin inhibitor nephrotoxicity.
50%的肾病综合征患儿使用免疫抑制剂以减少类固醇用量,预防复发和类固醇相关毒性。然而,环磷酰胺和他克莫司治疗后长期缓解的发生率及预测因素尚不确定。
对纳入纵向队列研究的1-18岁儿童进行回顾性分析。研究对象为1996年至2019年在加拿大多伦多诊断为类固醇敏感型肾病综合征的儿童。暴露因素为开始使用环磷酰胺或他克莫司。主要结局为长期缓解(无进一步复发或减少类固醇用量的免疫抑制治疗)。通过逻辑回归评估长期缓解和钙调神经磷酸酶抑制剂肾毒性的预测因素。
578例类固醇敏感型肾病综合征患儿中,252例接受环磷酰胺治疗,120例接受他克莫司治疗。中位随访5.4年(四分位间距2.4-9.1年),环磷酰胺治疗后72例(28.6%)实现长期缓解,他克莫司治疗后17例(14.2%)实现长期缓解。开始使用任何一种药物后复发频率均降低。既往复发率较低、治疗时间更近以及女性性别是环磷酰胺治疗后长期缓解的预测因素。将他克莫司作为第一种减少类固醇用量的药物是钙调神经磷酸酶抑制剂肾毒性的唯一预测因素。
虽然环磷酰胺或他克莫司均可降低短期复发率,但开始使用这两种药物后,不到三分之一的患儿实现长期缓解。很少有因素可预测环磷酰胺或他克莫司治疗后的长期缓解或钙调神经磷酸酶抑制剂肾毒性。