Division of Allergy and Clinical Immunology, Department of Chest Diseases, Erciyes University School of Medicine, Kayseri, Turkey.
Clinic of Immunological and Allergic Diseases, Kayseri Training and Research Center, Kayseri, Turkey.
Dermatol Ther. 2021 Jan;34(1):e14543. doi: 10.1111/dth.14543. Epub 2020 Nov 22.
The question how second-generation antihistamines (sgAHs) should be used when chronic spontaneous urticaria (CSU) is under control with omalizumab is still unanswered. This study aimed to investigate the effectiveness of as-needed sgAHs in patients with well-controlled urticaria under omalizumab treatment. Patients from four different urticaria centers who were treated with omalizumab 300 mg/4 weeks for at least 3 months, had well-controlled urticaria (Urticaria Control Test: 16 > UCT≥12) and were using sgAHs only if needed, were included in this study. In order to assess effectiveness of sgAHs, change in the itch, hives, and total itch-hives scores before and after sgAHs were evaluated using modified urticaria activity score-twice daily. Fifty-three patients [38 female (71.7%)] with mean age 41.1 ± 11.4 years were included in this study. Median sgAH intake per patient throughout the 4 week-intervals was 3 (2-5) tablets. sgAH intake decreased itch, hives and total itch-hives scores 45.7% ± 52.9, 42.4% ± 39.1, and 50.2% ± 51.1, respectively (P < .001 for all). This decrease was similar in both isolated-urticaria and urticaria-and-angioedema phenotypes. Baseline IgE levels were positively correlated with the decrease of three symptom scores (r = 0.31, P = .05; r = 0.375, P = .017; r = 0.31, P = .05, respectively) that showed in patients with higher baseline total IgE levels, as needed sgAH intake decreased the symptom scores less. Our study showed that sgAHs may still be an effective option for the treatment of the intermittent symptoms in patients with well-controlled urticaria under omalizumab treatment. Baseline total IgE levels may be used as a potential biomarker for sgAH effectiveness in these patients.
当慢性自发性荨麻疹(CSU)通过奥马珠单抗控制时,第二代抗组胺药(sgAHs)应该如何使用,这个问题仍然没有答案。本研究旨在探讨在奥马珠单抗治疗下荨麻疹得到良好控制的患者中按需使用 sgAHs 的疗效。本研究纳入了来自四个不同荨麻疹中心的患者,他们接受奥马珠单抗 300mg/4 周治疗至少 3 个月,荨麻疹得到良好控制(荨麻疹控制测试:16>UCT≥12),且仅在需要时使用 sgAHs。为了评估 sgAHs 的疗效,使用改良的每日两次荨麻疹活动评分(urticaria activity score-twice daily,UAS2)评估 sgAHs 前后瘙痒、风团和总瘙痒-风团评分的变化。本研究纳入了 53 名患者[38 名女性(71.7%)],平均年龄为 41.1±11.4 岁。在整个 4 周间隔内,每位患者平均服用 sgAHs 3(2-5)片。sgAHs 摄入使瘙痒、风团和总瘙痒-风团评分分别降低了 45.7%±52.9、42.4%±39.1 和 50.2%±51.1(P<.001 均)。在孤立性荨麻疹和荨麻疹伴血管性水肿表型中,这种降低是相似的。基线 IgE 水平与三种症状评分的降低呈正相关(r=0.31,P=0.05;r=0.375,P=0.017;r=0.31,P=0.05,分别),在基线总 IgE 水平较高的患者中,按需使用 sgAHs 摄入减少了症状评分。我们的研究表明,在奥马珠单抗治疗下荨麻疹得到良好控制的患者中,sgAHs 可能仍然是治疗间歇性症状的有效选择。基线总 IgE 水平可作为预测这些患者 sgAHs 疗效的潜在生物标志物。