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

医学 狼疮性肾炎 内科学 胃肠病学 肌酐 泼尼松龙 他克莫司 泌尿科 移植 疾病
作者
Hiroshi Tanaka,Eishin Oki,Koji Tsugawa,Kazuhito Nonaka,Koichi Suzuki,Etsuro Ito
出处
期刊:Lupus [SAGE]
卷期号:16 (11): 896-900 被引量:30
标识
DOI:10.1177/0961203307081914
摘要

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. Lupus (2007) 16, 896—900.
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