Graduate school, Tianjin Medical University, Tianjin, China.
Graduate school, Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Front Immunol. 2022 Jun 13;13:928621. doi: 10.3389/fimmu.2022.928621. eCollection 2022.
Bullous pemphigoid (BP) is the most common autoimmune subepidermal bullous disease of the skin. First-line treatment of systemic corticosteroids may cause serious adverse events. Rituximab, omalizumab, and dupilumab should be explored as alternative treatment options to improve outcomes.
To systematically review the rituximab, omalizumab, and dupilumab treatment outcomes in bullous pemphigoid.
A PubMed, Embase, Web of Science, and Cochrane library search were conducted on March 10, 2022. A total of 75 studies were included using Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines.
Use of rituximab (n=122), omalizumab (n=53) and dupilumab (n=36) were reported in 211 patients with BP. Rituximab led to complete remission in 70.5% (n=86/122) and partial remission in 23.8% (n=29/122) of patients within 5.7 months, with a recurrence rate of 20.5% (n=25/122). 9.0% (n=11/122) of patients died and infection (6.6%, n=8/122) was the most common adverse event. Omalizumab led to complete remission in 67.9% (n=36/53) and partial remission in 20.8% (n=11/53) of patients within 6.6 months, with a recurrence rate of 5.7% (n=3/53). 1.9% (n=1/53) of patients died and thrombocytopenia (1.9%, n=1/53) was observed as the most common adverse event. Dupilumab led to complete remission in 66.7% (n=24/36) and partial remission in 19.4% (n=7/36) of patients within 4.5 months of treatment without any reported adverse events, with a recurrence rate of 5.6% (n=2/36).
Rituximab, omalizumab, and dupilumab have similar clinical benefits for BP patients. However, rituximab resulted in higher recurrence rates, adverse events, and mortality rates.
https://www.crd.york.ac.uk/PROSPERO/, identifier CRD42022316454.
大疱性类天疱疮(BP)是皮肤最常见的自身免疫性表皮下大疱性疾病。一线治疗药物皮质类固醇可能会引起严重的不良反应。利妥昔单抗、奥马珠单抗和度普利尤单抗应作为替代治疗方案进行探索,以改善治疗效果。
系统综述利妥昔单抗、奥马珠单抗和度普利尤单抗治疗大疱性类天疱疮的效果。
于 2022 年 3 月 10 日在 PubMed、Embase、Web of Science 和 Cochrane 图书馆进行检索。采用系统评价和荟萃分析的 Preferred Reporting Items 指南纳入 75 项研究。
共纳入 211 例 BP 患者,分别使用利妥昔单抗(n=122)、奥马珠单抗(n=53)和度普利尤单抗(n=36)治疗。利妥昔单抗治疗后,5.7 个月内患者完全缓解率为 70.5%(n=86/122),部分缓解率为 23.8%(n=29/122),复发率为 20.5%(n=25/122)。9.0%(n=11/122)的患者死亡,感染(6.6%,n=8/122)是最常见的不良反应。奥马珠单抗治疗后,6.6 个月内患者完全缓解率为 67.9%(n=36/53),部分缓解率为 20.8%(n=11/53),复发率为 5.7%(n=3/53)。1.9%(n=1/53)的患者死亡,血小板减少症(1.9%,n=1/53)是最常见的不良反应。度普利尤单抗治疗后,4.5 个月内患者完全缓解率为 66.7%(n=24/36),部分缓解率为 19.4%(n=7/36),无任何不良反应报告,复发率为 5.6%(n=2/36)。
利妥昔单抗、奥马珠单抗和度普利尤单抗对 BP 患者的临床疗效相似。然而,利妥昔单抗导致更高的复发率、不良反应和死亡率。
https://www.crd.york.ac.uk/PROSPERO/,标识符 CRD42022316454。