Shah Bela, Dhoot Dhiraj, Choudhary Ankita, Jangid Neha, Mistry Deval, Shah Shikha, Kamat Shruti, Barkate Hanmant
Department of Dermatology, Venereology and Leprosy, B.J.Medical College, Civil Hospital, Ahmedabad, India.
DGM, Department of Global Medical Affairs, Glenmark Pharmaceuticals Ltd, Mumbai, India.
Clin Cosmet Investig Dermatol. 2022 Feb 18;15:261-270. doi: 10.2147/CCID.S350122. eCollection 2022.
Though second-generation antihistamines (SGAH) are first-line drugs in chronic spontaneous urticaria (CSU), 50% of patients do not respond to them. In such patients, guidelines recommend either up-dosing of SGAH or combination of different antihistamines. However, the studies comparing these treatment regimens are limited.
In this comparative, three-arm study, CSU patients were randomized to receive standard dose of either bilastine, fexofenadine, or levocetirizine for 2 weeks. After 2 weeks of treatment, non-responders received double dose of either bilastine or fexofenadine, while hydroxyzine 25 mg once daily was added in the levocetirizine group. Patients were primarily evaluated for improvement in CSU, quality of life, and somnolence.
A total of 110 patients with CSU were recruited. At the end of 4 weeks, 33/39, 26/35, and 22/36 patients in the bilastine, fexofenadine, and levocetirizine groups showed improvement in urticaria symptoms. At week 2, there was no statistical difference in urticaria activity score (UAS7) improvement between any of the groups; however, at week 4, there was a statistical difference between the bilastine and levocetirizine groups (<0.05). Somnolence was significantly lower in the bilastine group (<0.05). Bilastine was statistically significant (<0.05) in the improvement of quality of life as compared to both groups. No major adverse events were reported during study period; however, bilastine was associated with significantly lower levels of AEs compared to levocetirizine (<0.05).
Two-fold up-dosing of bilastine improves CSU symptoms without compromising safety as compared to two-fold up-dosing of fexofenadine and combination of first- and second-generation antihistamines.
尽管第二代抗组胺药(SGAH)是慢性自发性荨麻疹(CSU)的一线用药,但50%的患者对此无反应。对于此类患者,指南建议增加SGAH剂量或联合使用不同的抗组胺药。然而,比较这些治疗方案的研究有限。
在这项三臂对照研究中,CSU患者被随机分为三组,分别接受标准剂量的比拉斯汀、非索非那定或左西替利嗪治疗2周。治疗2周后,无反应者接受比拉斯汀或非索非那定双倍剂量治疗,而左西替利嗪组则每日加用25mg羟嗪。主要评估患者CSU症状的改善情况、生活质量和嗜睡情况。
共招募了110例CSU患者。4周结束时,比拉斯汀组、非索非那定组和左西替利嗪组分别有33/39、26/35和22/36例患者的荨麻疹症状得到改善。在第2周时,各组之间的荨麻疹活动评分(UAS7)改善情况无统计学差异;然而,在第4周时,比拉斯汀组和左西替利嗪组之间存在统计学差异(<0.05)。比拉斯汀组的嗜睡情况明显更低(<0.05)。与其他两组相比,比拉斯汀在改善生活质量方面具有统计学意义(<0.05)。研究期间未报告重大不良事件;然而,与左西替利嗪相比,比拉斯汀的不良事件发生率明显更低(<0.05)。
与非索非那定双倍剂量以及第一代和第二代抗组胺药联合使用相比,比拉斯汀双倍剂量可改善CSU症状且不影响安全性。