Department of Nephrology, AP-HP, Hôpital Tenon, Service de Néphrologie et Dialyses, Paris, France.
Kidney Int. 2013 Mar;83(3):511-6. doi: 10.1038/ki.2012.444. Epub 2013 Jan 16.
Development of steroid dependency in patients with nephrotic syndrome may require a long-term multi-drug therapy at risk of drug toxicity and renal failure. Rituximab treatment reduces the steroid dosage and the need for immunosuppressive therapy in pediatric patients. Here we retrospectively analyze the efficacy and safety of rituximab in adult patients with steroid-dependent minimal change disease. To do this, we analyzed the outcome of all adult patients treated with rituximab for steroid-dependent minimal change nephrotic syndrome over a mean follow-up of 29.5 months (range 5.1-82 months). Seventeen patients with steroid-dependent or frequently relapsing minimal change nephrotic syndrome, unresponsive to several immunosuppressive medications, were treated with rituximab. Eleven patients had no relapses after rituximab infusion (mean follow-up 26.7 months, range 5.1-82 months) and nine of them were able to come off all other immunosuppressive drugs and steroids during follow-up. Six patients relapsed at least once after a mean time of 11.9 months (mean follow-up 34.5 months, range 16.9-50.1 months), but their immunosuppressive drug treatment could be stopped or markedly reduced during this time. No adverse events were recorded. Thus, rituximab is efficient and safe in adult patients suffering from severe steroid-dependent minimal change disease. Prospective randomized trials are needed to confirm this study.
肾病综合征患者的类固醇依赖发展可能需要长期多药物治疗,存在药物毒性和肾衰竭的风险。利妥昔单抗治疗可降低儿科患者的类固醇剂量和免疫抑制治疗的需求。在这里,我们回顾性分析了利妥昔单抗治疗成人类固醇依赖性微小病变性肾病的疗效和安全性。为此,我们分析了所有接受利妥昔单抗治疗的成人类固醇依赖性微小病变性肾病患者的结局,平均随访 29.5 个月(范围 5.1-82 个月)。17 例类固醇依赖性或频繁复发的微小病变性肾病综合征患者对几种免疫抑制剂治疗无反应,接受了利妥昔单抗治疗。利妥昔单抗输注后 11 例患者无复发(平均随访 26.7 个月,范围 5.1-82 个月),其中 9 例在随访期间能够停用所有其他免疫抑制剂和类固醇。6 例患者在平均 11.9 个月后至少复发 1 次(平均随访 34.5 个月,范围 16.9-50.1 个月),但在此期间可以停用或显著减少免疫抑制剂治疗。未记录到不良反应。因此,利妥昔单抗治疗成人严重类固醇依赖性微小病变性肾病的疗效和安全性。需要前瞻性随机试验来证实这项研究。