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依那西普对难治性全身型幼年特发性关节炎的疗效。

Effect of etanercept on refractory systemic-onset juvenile idiopathic arthritis.

作者信息

Hu Xiao, Yuan Fang, Zhang Jian, Yin Lei, Li Bi-Ru, Jin Yan-Liang

机构信息

Department of Rheumatology, Shanghai Children's Medical Center, Shanghai Jiaotong University, School of Medicine, Shanghai, China.

出版信息

World J Pediatr. 2016 Feb;12(1):96-102. doi: 10.1007/s12519-015-0009-3. Epub 2015 Mar 9.

Abstract

BACKGROUND

Treatment of systemic-onset juvenile idiopathic arthritis (So-JIA) is challenging, and the efficacy of injectable recombinant human tumor necrosis factor type 1 receptor-antibody fusion protein (etanercept) on So-JIA has been controversial.

METHODS

We retrospectively studied 12 patients with refractory systemic juvenile arthritis treated with etanercept at our hospital in the past 5 years. The 12 patients were divided into a corticosteroid-dependent group (n=7) and an ineffective group (n=5) on the basis of their responses to treatment before the administration of etanercept. Etanercept was added to the treatment without substantially changing the original regimens in general, and doses, and signs of efficacy including alleviation or resolution of symptoms such as high fever, inflammatory arthropathy, eruption rash, hydrohymenitis, as well as changes in the levels of laboratory inflammatory markers such as the white blood cell count, erythrocyte sedimentation rate, levels of C-reactive protein and serum ferritin were recorded.

RESULTS

Etanercept was withdrawn after the first dose from one patient in the corticosteroid-dependent group because of a systemic allergic rash, and was also withdrawn from one patient in the ineffective group after 2 months of treatment owing to inefficacy; the remaining 10 patients completed the entire treatment protocol, at which point etanercept was discontinued. At that time, clinical symptoms and laboratory inflammatory markers of the remaining patients were within the normal range and the mean dose of prednisone was 0.18 mg/kg per day, an 81% decrease from the mean dose at baseline. At present, the corticosteroid has been discontinued and only methotrexate maintenance treatment is used in 3 patients; the other 7 patients are treated with prednisone and methotrexate maintenance therapy. All of the 10 patients are in a medicated remission with no recurrence.

CONCLUSIONS

In the treatment of patients with refractory So-JIA, the principles of individual therapy and combinations of drugs should be followed. Etanercept is an important and valid candidate for use in such combined treatment strategies.

摘要

背景

全身型幼年特发性关节炎(So-JIA)的治疗具有挑战性,注射用重组人肿瘤坏死因子Ⅰ型受体-抗体融合蛋白(依那西普)治疗So-JIA的疗效一直存在争议。

方法

我们回顾性研究了我院过去5年中用依那西普治疗的12例难治性全身型幼年特发性关节炎患者。根据依那西普给药前对治疗的反应,将这12例患者分为糖皮质激素依赖组(n=7)和无效组(n=5)。一般在不显著改变原治疗方案和剂量的基础上加用依那西普,并记录疗效体征,包括高热、炎症性关节病、皮疹、浆膜炎等症状的缓解或消退,以及白细胞计数、红细胞沉降率、C反应蛋白水平和血清铁蛋白等实验室炎症指标的变化。

结果

糖皮质激素依赖组1例患者在首次注射依那西普后因全身性过敏皮疹停药,无效组1例患者在治疗2个月后因无效停药;其余10例患者完成了整个治疗方案,此时停用依那西普。那时,其余患者的临床症状和实验室炎症指标均在正常范围内,泼尼松的平均剂量为每日0.18mg/kg,较基线平均剂量降低了81%。目前,3例患者已停用糖皮质激素,仅采用甲氨蝶呤维持治疗;另外7例患者采用泼尼松和甲氨蝶呤维持治疗。10例患者均处于药物缓解期,无复发。

结论

在难治性So-JIA患者的治疗中,应遵循个体化治疗和联合用药原则。依那西普是此类联合治疗策略中重要且有效的候选药物。

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