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外用SDZ ASM 981治疗儿童特应性皮炎的首次经验。

First experience of topical SDZ ASM 981 in children with atopic dermatitis.

作者信息

Harper J, Green A, Scott G, Gruendl E, Dorobek B, Cardno M, Burtin P

机构信息

Department of Paediatric Dermatology, Great Ormond Street Hospital for Children, London WC1 3JH, UK.

出版信息

Br J Dermatol. 2001 Apr;144(4):781-7. doi: 10.1046/j.1365-2133.2001.04133.x.

DOI:10.1046/j.1365-2133.2001.04133.x
PMID:11298537
Abstract

BACKGROUND

SDZ ASM 981 is a selective inhibitor of inflammatory cytokine release under development for the topical treatment of atopic dermatitis.

OBJECTIVES

This first paediatric study was designed to measure the systemic exposure to SDZ ASM 981 in young children with atopic dermatitis treated on extensive skin areas.

METHODS

Children 1-4 years of age referred to a tertiary care centre for their atopic dermatitis were treated twice daily for 3 weeks with 1% SDZ ASM 981 cream. SDZ ASM 981 blood concentrations were measured on day 4 and 22 (last day) of treatment, and 1 week after the last application, using a radioimmunoassay with a limit of quantification of 0.5 ng mL(-1). Efficacy was assessed by the Eczema Area Severity Index (EASI).

RESULTS

The 10 patients included had 23-69% of their body surface area (BSA) affected at baseline. Of the 63 SDZ ASM 981 blood concentrations measured, 63% were < 0.5 ng mL(-1); the maximum value observed was 1.8 ng mL-1. No accumulation was evidenced between days 4 and 22. The first two patients experienced a flare of atopic dermatitis that was not controlled by the study medication. In the other patients, the EASI improved by 8-89% at 3 weeks of treatment.

CONCLUSIONS

In these children 1-4 years of age, blood concentrations of SDZ ASM 981 during topical treatment with the 1% cream were consistently low even in the children with the most extensive areas treated (up to 69% of their BSA).

摘要

背景

SDZ ASM 981是一种炎症细胞因子释放的选择性抑制剂,正处于开发阶段,用于特应性皮炎的局部治疗。

目的

这项首次针对儿科患者的研究旨在测量在大面积皮肤区域接受治疗的特应性皮炎幼儿中SDZ ASM 981的全身暴露量。

方法

将1至4岁因特应性皮炎转诊至三级护理中心的儿童,每日两次使用1% SDZ ASM 981乳膏治疗,为期3周。在治疗的第4天和第22天(最后一天)以及最后一次用药后1周,使用定量限为0.5 ng/mL(-1)的放射免疫分析法测量SDZ ASM 981的血药浓度。通过湿疹面积和严重程度指数(EASI)评估疗效。

结果

纳入的10名患者在基线时体表面积(BSA)的23%-69%受到影响。在测量的63次SDZ ASM 981血药浓度中,63% < 0.5 ng/mL(-1);观察到的最大值为1.8 ng/mL-1。在第4天和第22天之间未发现药物蓄积。前两名患者出现了特应性皮炎发作,研究药物未能控制。在其他患者中,治疗3周时EASI改善了8%-89%。

结论

在这些1至4岁的儿童中,即使是治疗面积最大(高达其BSA的69%)的儿童,在局部使用1%乳膏治疗期间,SDZ ASM 981的血药浓度始终较低。

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