University College London Centre for Nephrology, Royal Free Campus, University College London, London, UK.
University College London Institute of Child Health, University College London, London, UK.
Nephrology (Carlton). 2016 Oct;21(10):893-900. doi: 10.1111/nep.12744.
Treatment of frequently relapsing or steroid-dependent minimal change disease (MCD) in children and adults remains challenging. Glucocorticoids and/or other immunosuppressive agents are the mainstay of treatment, but patients often experience toxicity from prolonged exposure and may either become treatment dependent and/or resistant. Increasing evidence suggests that rituximab (RTX) can be a useful alternative to standard immunosuppression and allow withdrawal of maintenance immunosuppressants; however, data on optimal treatment regimens, long-term efficacy and safety are still limited.
We undertook a prospective study of RTX to allow immunosuppression minimization in 15 young adults with frequently relapsing or steroid-dependent, biopsy-proven MCD. All patients were in remission at the start of treatment and on a calcineurin inhibitor. Two doses of RTX (1 gr) were given 6 months apart. A subset of patients also received an additional dose 12 months later, in order to examine the benefit of re-treatment. Biochemical and clinical parameters were monitored over an extended follow-up period of up to 43 months.
Median steroid-free survival after RTX was 25 months (range 4-34). Mean relapse frequency decreased from 2.60 ± 0.28 to 0.4 ± 0.19 (P < 0.001) after RTX. Seven relapses occurred, five of which (71%) when CD19 counts were greater than 100 µ. Immunoglobulin levels remained unchanged, and no major side effects were observed throughout the follow-up period.
Rituximab therapy is effective at maintaining prolonged steroid-free remission and reducing relapse frequency in this group of patients. Our study lends further support for the role of RTX in the treatment of patients with frequently relapsing or steroid-dependent MCD.
儿童和成人频繁复发或依赖激素的微小病变性肾病(MCD)的治疗仍然具有挑战性。糖皮质激素和/或其他免疫抑制剂是治疗的主要方法,但患者经常因长期暴露而出现毒性,并且可能依赖治疗或产生耐药性。越来越多的证据表明,利妥昔单抗(RTX)可以作为标准免疫抑制的替代方法,并允许停用维持性免疫抑制剂;然而,关于最佳治疗方案、长期疗效和安全性的数据仍然有限。
我们进行了一项前瞻性研究,在 15 名年轻成人中使用 RTX 来最小化免疫抑制,这些患者患有频繁复发或依赖激素的、经活检证实的 MCD。所有患者在开始治疗时和使用钙调神经磷酸酶抑制剂时均处于缓解期。每隔 6 个月给予 RTX 两剂(1g)。一部分患者还在 12 个月后接受了额外的剂量,以检查重新治疗的益处。在长达 43 个月的扩展随访期间监测生化和临床参数。
RTX 后的无激素生存中位数为 25 个月(范围 4-34)。RTX 后,平均复发频率从 2.60±0.28 降至 0.4±0.19(P<0.001)。发生了 7 次复发,其中 5 次(71%)发生在 CD19 计数大于 100µ时。免疫球蛋白水平保持不变,整个随访期间未观察到主要副作用。
利妥昔单抗治疗可有效维持长期无激素缓解并降低该组患者的复发频率。我们的研究进一步支持 RTX 在治疗频繁复发或依赖激素的 MCD 患者中的作用。