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托珠单抗对长期接受糖皮质激素治疗的全身型幼年特发性关节炎生长障碍的影响。

Effect of tocilizumab on growth impairment in systemic juvenile idiopathic arthritis with long-term corticosteroid therapy.

作者信息

Miyamae Takako, Yokoya Susumu, Yamanaka Hisashi, Yokota Shumpei

机构信息

Department of Pediatrics, Yokohama City University , Yokohama , Japan.

出版信息

Mod Rheumatol. 2014 Jul;24(4):567-71. doi: 10.3109/14397595.2013.844404. Epub 2013 Oct 21.

Abstract

BACKGROUND

The safety and efficacy of tocilizumab (TCZ), an anti-IL-6 receptor monoclonal antibody, have been reported in the treatment of children with systemic juvenile idiopathic arthritis (sJIA).

OBJECTIVES

Growth of children during the TCZ study was analyzed.

METHODS

Forty-five sJIA patients (8.1 ± 4.2 years) were enrolled. Mean standard deviation score (SDS) for height (HTSDS), height velocity (HVSDS) and changes in SDS from baseline (∆SDS) were determined. Correlation between ∆SDS and several factors such as age, disease duration and corticosteroid exposure were evaluated. Yearly height velocity was analyzed for 28 patients for whom we had data for 1 year prior to TCZ administration and who had received TCZ for more than 1 year.

RESULTS

Of the 45 patients, 38 (84%) obtained a clinical response at week 144. The mean baseline HTSDS was - 2.7 ± 2.0 and inversely correlated with disease duration. Significant improvement was seen in change in HVSDS from 1 year prior to 1 year after baseline (- 6.0 ± 4.0 to - 2.5 ± 3.9, p = 0.0064). Reduction in corticosteroid exposure was significantly associated with improvement in HVSDS (p = 0.0027).

CONCLUSIONS

Growth impairment evidenced by HTSDS was more prominent in patients with longer standing disease. Catch-up growth was observed in patients who required less or no corticosteroid during TCZ treatment.

摘要

背景

抗白细胞介素6受体单克隆抗体托珠单抗(TCZ)治疗儿童全身型幼年特发性关节炎(sJIA)的安全性和有效性已有报道。

目的

分析托珠单抗研究期间儿童的生长情况。

方法

纳入45例sJIA患者(8.1±4.2岁)。测定身高的平均标准差评分(HTSDS)、身高速度(HVSDS)以及与基线相比的标准差变化(∆SDS)。评估∆SDS与年龄、病程和皮质类固醇暴露等几个因素之间的相关性。对28例在使用托珠单抗前有1年数据且接受托珠单抗治疗超过1年的患者进行了年度身高速度分析。

结果

45例患者中,38例(84%)在第144周获得临床缓解。平均基线HTSDS为-2.7±2.0,与病程呈负相关。从基线前1年到基线后1年,HVSDS变化有显著改善(-6.0±4.0至-2.5±3.9,p = 0.0064)。皮质类固醇暴露的减少与HVSDS的改善显著相关(p = 0.0027)。

结论

病程较长的患者中,HTSDS所证明的生长障碍更为突出。在托珠单抗治疗期间需要较少或不需要皮质类固醇的患者中观察到了追赶生长。

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