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奥马珠单抗治疗青少年慢性自发性荨麻疹:疗效和安全性。

Omalizumab treatment in adolescents with chronic spontaneous urticaria: Efficacy and safety.

机构信息

Hacettepe University Faculty of Medicine, Department of Pediatric Allergy, 06100 Ankara, Turkey.

Hacettepe University Faculty of Medicine, Department of Pediatric Allergy, 06100 Ankara, Turkey.

出版信息

Allergol Immunopathol (Madr). 2020 Jul-Aug;48(4):368-373. doi: 10.1016/j.aller.2020.03.011. Epub 2020 May 25.

DOI:10.1016/j.aller.2020.03.011
PMID:32467066
Abstract

BACKGROUND

Omalizumab is useful as an add-on treatment in patients unresponsive to high doses of second-generation antihistamines. This study aimed to evaluate the efficacy and safety of omalizumab treatment in adolescents with refractory chronic spontaneous urticaria (CSU).

METHODS

CSU patients aged 12-18 years old with the diagnosis of symptomatic CSU and unresponsive to classical treatment were included in the study. All patients had an urticaria-activity-score (UAS7) of ≥16 or and were treated with 300mg omalizumab every four weeks. The degree of response was classified into complete, partial and non-responders due to UAS7.

RESULTS

A total of 29 patients were evaluated. The median age and symptom onset age of the patients was 15.2 (IQR, 12.8-16.5) years and 14.0 (IQR, 11.8-15.9) years, respectively. The median duration of urticaria was eight (IQR, 4-24) months at admission. Eleven (37.9%) patients had angioedema and ten (34.5%) patients had concomitant allergic diseases. The median age at the beginning of treatment with omalizumab was 15.4 (IQR, 12.9-16.9) years. The median symptom duration was 12 (IQR, 6.5-27.5) months before the omalizumab treatment. Twenty-eight (96.5%) of the patients (89.6% complete, 6.9% partial) achieved response; however, one patient was a non-responder (3.5%). The adverse effect was observed in one (3.4%) patient as angioedema after the third dose. Twenty-three patients were followed up for a median of 18 (IQR, 13-27) months. Relapse was observed in three (13%) patients.

CONCLUSIONS

Omalizumab is considered as an effective and safe treatment for CSU in adolescents. Relapses mostly occur within the first year after the cessation of treatment.

摘要

背景

奥马珠单抗作为二线抗组胺药物治疗抵抗患者的附加治疗是有效的。本研究旨在评估奥马珠单抗治疗青少年难治性慢性自发性荨麻疹(CSU)的疗效和安全性。

方法

纳入诊断为症状性 CSU 且对经典治疗无反应的 12-18 岁 CSU 患者。所有患者的荨麻疹活动评分(UAS7)≥16 或对奥马珠单抗 300mg 每四周一次的治疗有反应。根据 UAS7 将反应程度分为完全、部分和无反应者。

结果

共评估了 29 例患者。患者的中位年龄和症状发病年龄分别为 15.2(IQR,12.8-16.5)岁和 14.0(IQR,11.8-15.9)岁。入院时荨麻疹的中位病程为 8(IQR,4-24)个月。11 例(37.9%)患者有血管性水肿,10 例(34.5%)患者有合并的过敏性疾病。开始奥马珠单抗治疗的中位年龄为 15.4(IQR,12.9-16.9)岁。奥马珠单抗治疗前的中位症状持续时间为 12(IQR,6.5-27.5)个月。28 例(96.5%)患者(89.6%完全缓解,6.9%部分缓解)达到缓解;然而,1 例患者无反应(3.5%)。1 例(3.4%)患者在第三次剂量后出现血管性水肿的不良反应。23 例患者中位随访 18(IQR,13-27)个月。3 例(13%)患者复发。

结论

奥马珠单抗被认为是青少年 CSU 的一种有效且安全的治疗方法。停药后第一年复发较多。

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