Pediatric Department, University Hospital of Nantes, Nantes, France.
Service de Maladies Chroniques de l'enfant, Hôpital femme-enfants-adolescent, CHU Nantes, 7, quai Moncousu, 44093, Cedex Nantes, France.
Pediatr Nephrol. 2020 Aug;35(8):1499-1506. doi: 10.1007/s00467-020-04567-7. Epub 2020 Apr 18.
Relapsing nephrotic syndrome (NS) after transplantation can be a challenge to treat. The result of the consequent long-lasting proteinuria is the loss of the graft. Disease recurrence after renal transplantation occurs in around half of cases, and the efficacy of therapeutic strategies is often limited. Recently, ofatumumab, a second-generation and fully human anti-CD20 monoclonal antibody, has been shown to be effective in severe situations.
We retrospectively collected data from the medical records of children with recurrence of NS after renal transplantation treated with ofatumumab in France, after failure of previous treatments.
Six patients were included in this study in five centers with a median duration of follow-up of 10.5 months. Two different ofatumumab regimens were administered. The primary outcome was proteinuria at 6 months after the last dose of ofatumumab. No patient achieved a complete remission, 3/6 had a partial remission, and 3/6 had no response to ofatumumab. Four patients exhibited a minor allergic reaction with the first infusion. One patient died of infection, as a consequence of multiple factors. No malignancies were observed; however, the time of follow-up was not sufficient to see such disease.
Altogether, these results suggest ofatumumab has a poor efficacy in treating recurrence of NS after renal transplantation. However, it could be discussed in multidrug-resistant refractory NS, but infectious complications and overimmunosuppression have to be balanced. There is a need for further studies to confirm these findings and safety and to determine a standardized protocol in this indication.
移植后复发性肾病综合征(NS)的治疗颇具挑战。长期大量蛋白尿会导致移植物丢失。约半数肾移植后会发生疾病复发,且治疗策略的疗效往往有限。最近,第二代、全人源抗 CD20 单克隆抗体奥法妥珠单抗已被证明对严重情况有效。
我们回顾性地收集了法国五家中心的儿童肾移植后复发 NS 患者在先前治疗失败后使用奥法妥珠单抗治疗的数据。
本研究共纳入了 6 名患者,中位随访时间为 10.5 个月。使用了两种不同的奥法妥珠单抗方案。主要终点是最后一次奥法妥珠单抗治疗后 6 个月的蛋白尿。没有患者完全缓解,6 例中有 3 例部分缓解,3 例对奥法妥珠单抗无反应。4 例患者首次输注时出现轻微过敏反应。1 例患者因多种因素感染死亡。未观察到恶性肿瘤;然而,随访时间不足以观察到此类疾病。
总的来说,这些结果表明奥法妥珠单抗治疗肾移植后 NS 复发的疗效不佳。然而,对于多药耐药性难治性 NS,可以考虑使用,但需要平衡感染并发症和过度免疫抑制。需要进一步的研究来证实这些发现和安全性,并确定该适应证的标准化方案。