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每日单次给予他克莫司有效治疗儿童期起病、病程较长的狼疮性肾炎年轻患者:一项开放标签的试点研究。

Effective treatment of young patients with pediatric-onset, long-standing lupus nephritis with tacrolimus given as a single daily dose: an open-label pilot study.

作者信息

Tanaka H, Oki E, Tsugawa K, Nonaka K, Suzuki K, Ito E

机构信息

Department of Pediatrics, Hirosaki University School of Medicine, Hirosaki, Japan.

出版信息

Lupus. 2007;16(11):896-900. doi: 10.1177/0961203307081914.

Abstract

The objective of the current work is to report the preliminary experience with tacrolimus (TL) administered as a single-dose daily for maintenance therapy of young patients with pediatric-onset, long-standing systemic lupus erythematosus (SLE). Six consecutive patients with long-standing SLE were recruited for a 6-month open-label trial of single-dose-daily administration of tacrolimus (3 mg/day) without dose up of concomitantly administered prednisolone (PDN). TL treatment was started at the time of the most recent flares. Data on the clinical and serologic lupus activity were collected prospectively. The baseline characteristics of the patients were: mean age, 20 years; urinary protein/creatinine ratio, 1.22 +/- 1.94; serum C3 level, 70.8 +/- 21.2 (normal, 79-152 mg/dL); serum complement hemolytic activity (CH50), 22.2 +/- 10.3 (normal, 23-46 U/mL); serum anti-dsDNA antibody titer, 60.4 +/- 71.7 IU/mL (normal, < 12.0 IU/mL); serum creatinine, 0.55 +/- 0.11 mg/dL; European Consensus Lupus Activity Measurement (ECLAM) index, 5.2 +/- 2.6. Despite the gradual tapering of the PDN dose, marked improvement as compared with the baseline values was observed in the ECLAM index examined at one and three months and serological parameters examined at three months after the start of treatment. After a 6-months' therapy, complete response was achieved in all of the patients (serum CH50 value, 27.7 +/- 8.3 U/mL; serum anti-dsDNA antibody titer, 28.4 +/- 27.9 U/mL and the ECLAM index, 1.2 +/- 1.2 (P < 0.05), respectively), except in one patient who showed WHO class V lupus nephritis. No serious adverse effects were observed. These data suggest that TL, even when administered as a single-daily dose, is effective and safe for selected young patients with pediatric-onset, long-standing SLE. However, further studies on a larger number of patients are needed to confirm these results.

摘要

本研究的目的是报告他克莫司(TL)单剂量每日给药用于儿科发病、病程较长的系统性红斑狼疮(SLE)年轻患者维持治疗的初步经验。连续招募了6例病程较长的SLE患者,进行为期6个月的他克莫司单剂量每日给药(3mg/天)的开放标签试验,同时不增加泼尼松龙(PDN)的剂量。TL治疗在最近一次病情发作时开始。前瞻性收集临床和血清学狼疮活动数据。患者的基线特征为:平均年龄20岁;尿蛋白/肌酐比值1.22±1.94;血清C3水平70.8±21.2(正常范围79 - 152mg/dL);血清补体溶血活性(CH50)22.2±10.3(正常范围23 - 46U/mL);血清抗双链DNA抗体滴度60.4±71.7IU/mL(正常范围<12.0IU/mL);血清肌酐0.55±0.11mg/dL;欧洲狼疮活动共识测量(ECLAM)指数5.2±2.6。尽管PDN剂量逐渐减少,但在治疗开始后1个月和3个月检查的ECLAM指数以及3个月检查的血清学参数方面,与基线值相比仍有显著改善。经过6个月的治疗,除1例表现为WHO V级狼疮性肾炎的患者外,所有患者均实现完全缓解(血清CH50值27.7±8.3U/mL;血清抗双链DNA抗体滴度28.4±27.9U/mL,ECLAM指数1.2±1.2(P<0.05))。未观察到严重不良反应。这些数据表明,TL即使单剂量每日给药,对选定的儿科发病、病程较长的SLE年轻患者也是有效且安全的。然而,需要对更多患者进行进一步研究以证实这些结果。

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