Alomari Omar, Ozceker Deniz, Mokresh Muhammed Edib, Topçak Asli Berivan, Ertan Sinem Nur, Şahin Merve Karaca, Çalışkan Nilay, Karadag Sefika Ilknur Kökcü, Erbay Muhammed Fatih, Yıldırım Güler, Bologur Hamit, Güngör Hilal, Kaplan Ozlem, Tunç Hasan Sarman, Göncü Emek Kocatürk
Hamidiye International School of Medicine, University of Health Sciences, Istanbul, Turkey.
Department of Pediatric Allergy and Immunology, University of Health Sciences, Prof. Dr. Cemil Tascioglu City Hospital, Istanbul, Turkey.
Pediatr Allergy Immunol. 2025 Jun;36(6):e70132. doi: 10.1111/pai.70132.
Chronic spontaneous urticaria significantly impairs quality of life in children, with limited treatment options beyond antihistamines. Omalizumab, an anti-IgE antibody, has shown promise in adults but data on its use in children, especially those under 12, are scarce. This systematic review and meta-analysis aim to evaluate the efficacy and safety of omalizumab in pediatric chronic spontaneous urticaria, providing insights to inform clinical practice and future guidelines. PubMed, Scopus, Embase, Cochrane, and Web of Science databases have been searched for relevant studies. The "R" software has been utilized to analyze the response and relapse rates, changes in urticaria scores, and adverse event rates. Subgroup analyses were also done based on response rate. The assessment of heterogeneity utilized the I and chi-squared tests, applying the random effect model. This systematic review included 36 studies met the inclusion criteria. The pooled response rate for omalizumab was 88.0% (95% CI: 80.7%-95.2%; I = 61.0%; p = .001), with a complete response rate of 51.0% (95% CI: 32.7%-69.2%; I = 90.0%; p < .001). Good or well-controlled response rates were 50.5% (95% CI: 33.9%-67.1%; I = 54.2%; p = .068), while poor or partial responses were 20.1% (95% CI: 14.3%-27.3%; I = 0.0%; p = .787). Relapse rate were 24.3% (95% CI: 8.1%-40.6%; I = 66.6%; p = .006). The Urticaria Activity Score showed a significant mean reduction in symptoms (SMD = -3.08; 95% CI: -5.45 to -0.71; I = 89.1%; p < .001). Adverse events occurred in 3.4% of patients, with specific events including urticaria, angioedema, headaches, fatigue, flu-like symptoms, and mild joint pain. In pediatric patients under 12 years, 18 out of 21 achieved complete response, with a median age of 8 years and follow-up durations between 4 and 18 months. Adverse events in this group included serum sickness in one patient. Omalizumab appears to be an effective treatment option for chronic spontaneous urticaria, demonstrating effectiveness in improving symptoms and providing significant relief. The treatment is generally well-tolerated, with adverse events being rare and manageable. Overall, omalizumab contributing to better disease management and quality of life.
慢性自发性荨麻疹严重影响儿童的生活质量,除抗组胺药外,治疗选择有限。奥马珠单抗是一种抗IgE抗体,已在成人中显示出疗效,但关于其在儿童尤其是12岁以下儿童中使用的数据很少。本系统评价和荟萃分析旨在评估奥马珠单抗治疗儿童慢性自发性荨麻疹的疗效和安全性,为临床实践和未来指南提供参考依据。检索了PubMed、Scopus、Embase、Cochrane和Web of Science数据库中的相关研究。使用“R”软件分析缓解率和复发率、荨麻疹评分变化及不良事件发生率。还根据缓解率进行了亚组分析。采用I²检验评估异质性,并应用随机效应模型。本系统评价纳入了36项符合纳入标准的研究。奥马珠单抗的合并缓解率为88.0%(95%CI:80.7%-95.2%;I²=61.0%;p=0.001),完全缓解率为51.0%(95%CI:32.7%-69.2%;I²=90.0%;p<0.001)。良好或控制良好的缓解率为50.5%(95%CI:33.9%-67.1%;I²=54.2%;p=0.068),而差或部分缓解率为20.1%(95%CI:14.3%-27.3%;I²=0.0%;p=0.787)。复发率为24.3%(95%CI:8.1%-40.6%;I²=66.6%;p=0.006)。荨麻疹活动评分显示症状平均显著减轻(SMD=-3.08;95%CI:-5.45至-0.71;I²=89.1%;p<0.001)。3.4%的患者发生不良事件,具体事件包括荨麻疹、血管性水肿、头痛、疲劳、流感样症状和轻度关节疼痛。在12岁以下的儿科患者中,21例中有18例达到完全缓解,中位年龄为8岁,随访时间为4至18个月。该组中的不良事件包括1例患者发生血清病。奥马珠单抗似乎是治疗慢性自发性荨麻疹的有效选择,在改善症状和提供显著缓解方面显示出有效性。该治疗总体耐受性良好,不良事件罕见且可管理。总体而言,奥马珠单抗有助于更好地管理疾病和提高生活质量。