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利妥昔单抗在高剂量激素依赖型肾病综合征患儿从环孢素转换为霉酚酸酯过程中的积极作用。

Positive role of rituximab in switching from cyclosporine to mycophenolate mofetil for children with high-dose steroid-dependent nephrotic syndrome.

作者信息

Fujinaga Shuichiro, Sakuraya Koji, Yamada Akifumi, Urushihara Yasuko, Ohtomo Yoshiyuki, Shimizu Toshiaki

机构信息

Division of Nephrology, Saitama Children's Medical Center, 2100 Magome, Iwatsuki-ku, Saitama-city, Saitama, Japan,

出版信息

Pediatr Nephrol. 2015 Apr;30(4):687-91. doi: 10.1007/s00467-014-3034-x. Epub 2015 Jan 10.

Abstract

BACKGROUND

Recent randomized studies indicate that mycophenolate mofetil (MMF) is inferior to cyclosporine (CsA) in preventing relapses of nephrotic syndrome (NS). During the last decade, rituximab (RTX) has emerged as a rescue therapy in patients with complicated, frequently relapsing, or steroid-dependent NS.

CASE-DIAGNOSIS/TREATMENT: After introducing RTX in our single center, we analyzed 26 patients with steroid-dependent NS who had relapses while receiving long-term CsA and who were subsequently switched to MMF. MMF was adjusted to maintain a targeted predose mycophenolic acid (MPA) level of 2-5 μg/ml. Moreover, for patients who required MMF and high-dose prednisolone (PSL) to maintain remission, a single infusion of RTX (375 mg/m(2)) was added. The primary endpoint was the probability of achieving PSL-free remission for >1 year. At a mean follow-up of 28.8 ± 9.9 months, 11 of 26 patients (42 %) required RTX treatment, and 22 of those patients (85 %) achieved PSL-free sustained remission. The mean predose MPA levels for patients who achieved PSL-free sustained remission were significantly higher compared with those for patients who did not (3.1 μg/ml vs. 1.7 μg/ml, p < 0.05).

CONCLUSIONS

After RTX introduction, most patients were able to switch from CsA to MMF and achieve sustained PSL-free remission.

摘要

背景

近期的随机研究表明,在预防肾病综合征(NS)复发方面,霉酚酸酯(MMF)不如环孢素(CsA)。在过去十年中,利妥昔单抗(RTX)已成为复杂、频繁复发或依赖类固醇的NS患者的挽救疗法。

病例诊断/治疗:在我们的单中心引入RTX后,我们分析了26例依赖类固醇的NS患者,这些患者在接受长期CsA治疗时复发,随后改用MMF。调整MMF剂量以维持霉酚酸(MPA)给药前目标水平为2 - 5μg/ml。此外,对于需要MMF和高剂量泼尼松龙(PSL)以维持缓解的患者,加用单次输注RTX(375mg/m²)。主要终点是实现无PSL缓解超过1年的概率。平均随访28.8±9.9个月,26例患者中有11例(42%)需要RTX治疗,其中22例(85%)实现了无PSL持续缓解。实现无PSL持续缓解的患者的平均MPA给药前水平显著高于未实现的患者(3.1μg/ml对1.7μg/ml,p<0.05)。

结论

引入RTX后,大多数患者能够从CsA转换为MMF并实现无PSL持续缓解。

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