Jundong Huang, Jia Jian, Tingting Li, Min Li, Kaifu Luo, Sihan Deng, Yan Tang, Fangfen Liu, Zhixiang Zhao, Wei Shi, Ji Li
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Clinical outcome measures (Severity of Alopecia Tool, SALT) and adverse events (AEs) were analyzed. In addition, a literature review was conducted to summarize the efficacy of AA with dupilumab and the characteristics of patients previously reported in the literature.</p><p><strong>Results: </strong>We identified 10 patients with AA who were or are being treated with dupilumab, with a median (range) treatment duration of 8 (3-15) months. Of these, four patients have high serum immunoglobulin E (IgE) levels (≥200IU/ml). The mean (IQR) pretreatment SALT score was 79% (52-100). Seven of 10 patients achieved at least 50% re-growth. Of those who improved, the mean (IQR) percentage change in SALT score at 3 months and the end of follow-up was 57% (29%-89%) and 95% (68-100), respectively. Notably, seven patients (70%) had white hair regrowth, with the white hair slowly decreasing over time and the proportion of pigmented black hair increasing. Dupilumab was well tolerated by all patients. No adverse events were reported.</p><p><strong>Conclusions: </strong>Overall, our research supports dupilumab as another candidate that possesses potential benefits for AA. 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引用次数: 0
摘要
背景:越来越多的研究支持 TH2 轴在斑秃(AA)中的重要作用。杜匹鲁单抗是一种针对 IL-4Rα 的人源化单克隆抗体,可下调 TH2 反应。虽然在临床试验中显示出了疗效,但在 AA 患者中使用杜匹单抗的实际数据却很有限:报告 10 例接受杜比单抗治疗的 AA 患者的系列病例,并提供有关杜比单抗治疗重症 AA 疗效的实际证据:在这项回顾性单中心研究中,纳入了2022年5月至2023年10月期间接受过杜比鲁单抗治疗的所有AA患者。对临床结果指标(脱发严重程度工具,SALT)和不良事件(AEs)进行了分析。此外,我们还进行了文献综述,总结了使用杜必鲁单抗治疗AA的疗效以及之前文献报道的患者特征:结果:我们发现有10名AA患者曾经或正在接受杜比单抗治疗,中位(范围)治疗时间为8(3-15)个月。其中,4 名患者的血清免疫球蛋白 E (IgE) 水平较高(≥200IU/ml)。治疗前 SALT 评分的平均值(IQR)为 79% (52-100)。10 位患者中有 7 位至少实现了 50%的再生长。在病情好转的患者中,3 个月和随访结束时 SALT 评分的平均(IQR)百分比变化分别为 57% (29%-89%) 和 95% (68-100)。值得注意的是,7 名患者(70%)的白发重新生长,随着时间的推移,白发慢慢减少,色素沉着的黑发比例增加。所有患者对杜比鲁单抗的耐受性良好。无不良反应报告:总之,我们的研究支持将杜比鲁单抗作为另一种对 AA 有潜在益处的候选药物。高水平的 IgE 可能不是杜利单抗成功治疗的先决条件。
Dupliumab therapy for alopecia areata: a case series and review of the literature.
Background: A growing body of research supports the important role of the TH2 axis in alopecia areata (AA). Dupilumab is a humanized monoclonal antibody against IL-4Rα that downregulates TH2 response. Although efficacy has been shown in clinical trials, real-world data on the use of dupilumab in AA patients is limited.
Objectives: To report on a case series of 10 patients with AA who were treated with dupilumab and provide real-world evidence regarding its efficacy in treating severe AA.
Methods: In this retrospective single-center study, all AA patients treated with dupilumab treatment were included between May 2022 and October 2023. Clinical outcome measures (Severity of Alopecia Tool, SALT) and adverse events (AEs) were analyzed. In addition, a literature review was conducted to summarize the efficacy of AA with dupilumab and the characteristics of patients previously reported in the literature.
Results: We identified 10 patients with AA who were or are being treated with dupilumab, with a median (range) treatment duration of 8 (3-15) months. Of these, four patients have high serum immunoglobulin E (IgE) levels (≥200IU/ml). The mean (IQR) pretreatment SALT score was 79% (52-100). Seven of 10 patients achieved at least 50% re-growth. Of those who improved, the mean (IQR) percentage change in SALT score at 3 months and the end of follow-up was 57% (29%-89%) and 95% (68-100), respectively. Notably, seven patients (70%) had white hair regrowth, with the white hair slowly decreasing over time and the proportion of pigmented black hair increasing. Dupilumab was well tolerated by all patients. No adverse events were reported.
Conclusions: Overall, our research supports dupilumab as another candidate that possesses potential benefits for AA. High levels of IgE may be not prerequisites for dupilumab's successful treatment response.