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度普利尤单抗治疗木村病的疗效和安全性。

Efficacy and safety of dupilumab in the treatment of Kimura's disease.

机构信息

Department of Dermatology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.

出版信息

QJM. 2024 Aug 1;117(8):575-580. doi: 10.1093/qjmed/hcae048.

Abstract

BACKGROUND

Kimura's disease (KD) is a rare chronic inflammatory condition characterized by nodules and lymphadenopathy in the head and neck region, exhibiting type II inflammation. Dupilumab is commonly used against type II inflammation.

AIM

To evaluate the efficacy and safety of dupilumab in KD patients.

DESIGN

The real-world study was conducted in a hospital in China.

METHODS

Six male patients with a mean age of 24.50 ± 15.47 years were treated with dupilumab following the same protocol as that for atopic dermatitis (AD). Clinical and laboratory indicators, such as maximum nodule diameter, blood eosinophil count, eosinophil percentage, and total serum IgE levels were assessed at baseline, Week 12 and Week 24. Adverse events were documented. Paired t-tests and one-way ANOVA were used for statistical analysis.

RESULTS

The results showed significant reductions in the longest nodule diameter at Week 12 (P = 0.006) and Week 24 (P = 0.017) compared to baseline. Blood eosinophil count decreased by 57.95% (P = 0.024) at Week 12 and 90.59% (P = 0.030) at Week 24. Eosinophil percentage decreased by 58.44% (P = 0.026) at Week 12 and 89.37% (P = 0.013) at Week 24. Total serum IgE levels decreased by 78.02% (P = 0.040) at Week 12 and 89.55% (P = 0.031) at Week 24. The presence of AD did not affect the results. One patient experienced temporary facial erythema after 32 weeks of treatment, which resolved with topical treatment. No other adverse events were reported.

CONCLUSION

Dupilumab demonstrated effectiveness in treating KD without severe adverse events.

摘要

背景

木村病(KD)是一种罕见的慢性炎症性疾病,其特征是头颈部出现结节和淋巴结病,表现为 II 型炎症。度普利尤单抗常用于治疗 II 型炎症。

目的

评估度普利尤单抗治疗 KD 患者的疗效和安全性。

设计

本研究为中国某医院的真实世界研究。

方法

6 名男性患者,平均年龄 24.50±15.47 岁,按照特应性皮炎(AD)的相同方案接受度普利尤单抗治疗。在基线、12 周和 24 周时评估最大结节直径、血嗜酸性粒细胞计数、嗜酸性粒细胞百分比和总血清 IgE 水平等临床和实验室指标。记录不良反应。采用配对 t 检验和单因素方差分析进行统计学分析。

结果

结果显示,与基线相比,12 周(P=0.006)和 24 周(P=0.017)时最长结节直径显著缩小。血嗜酸性粒细胞计数在 12 周时下降 57.95%(P=0.024),在 24 周时下降 90.59%(P=0.030)。嗜酸性粒细胞百分比在 12 周时下降 58.44%(P=0.026),在 24 周时下降 89.37%(P=0.013)。总血清 IgE 水平在 12 周时下降 78.02%(P=0.040),在 24 周时下降 89.55%(P=0.031)。AD 的存在不影响结果。1 例患者在治疗 32 周后出现短暂的面部红斑,经局部治疗后缓解。未报告其他不良反应。

结论

度普利尤单抗治疗 KD 有效,且无严重不良反应。

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