Kianfar Nika, Dasdar Shayan, Marashi Amir, Tavakolpour Soheil, Mahmoudi Hamidreza, Daneshpazhooh Maryam
Drs. Kianfar, Dasdar, Marashi, Mahmoudi, and Daneshpazhooh are with the Autoimmune Bullous Diseases Research Center at Tehran University of Medical Sciences in Tehran, Iran.
Dr. Tavakolpour is with the Dana-Farber Cancer Institute, Harvard Medical School in Boston, Massachusetts.
J Clin Aesthet Dermatol. 2024 Jul;17(7):24-36.
Epidermolysis bullosa acquisita (EBA) is a rare dermatosis of the mucous membrane and/or skin. Employing biologic treatment modalities, specifically rituximab (RTX), have become pivotal measure in treating patients with blistering diseases. This study aims to summarize the current evidence on the safety and efficacy of RTX in EBA.
An extensive search was performed in MEDLINE/PubMed, Embase, Scopus, and Web of Science databases until the end of August 19th, 2023. Two independent reviewers screened the papers, and collected data. Two hundred thirty-three studies were screened using Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines.
Thirty-one studies were enrolled. The most common reason of RTX administration in patients with EBA was recalcitrant diseases. Clinical response and disease remission was recorded as 92.7 percent (63 patients) and 73.8 percent (45 patients) of the patients, respectively. A relapse rate of 39.5 percent (15 patients) in the mean follow-up of 23.0 months was reported in the studies. Of the patients, 28.2 percent (11 patients) experienced RTX-related side events, mostly mild and transient infusion reactions.
The results of this systematic review demonstrated that RTX is safe and effective in patients with EBA. This biological treatment modality can be routinely used in managing EBA.
获得性大疱性表皮松解症(EBA)是一种罕见的黏膜和/或皮肤疾病。采用生物治疗方法,特别是利妥昔单抗(RTX),已成为治疗水疱性疾病患者的关键措施。本研究旨在总结RTX治疗EBA的安全性和有效性的现有证据。
在MEDLINE/PubMed、Embase、Scopus和Web of Science数据库中进行了广泛检索,直至2023年8月19日。两名独立评审员筛选论文并收集数据。使用系统评价和Meta分析的首选报告项目指南筛选了233项研究。
纳入31项研究。EBA患者使用RTX的最常见原因是疾病难治。记录的临床反应和疾病缓解率分别为92.7%(63例患者)和73.8%(45例患者)。研究报告平均随访23.0个月时复发率为39.5%(15例患者)。患者中,28.2%(11例患者)发生了与RTX相关的不良事件,大多为轻度和短暂的输注反应。
本系统评价结果表明,RTX对EBA患者安全有效。这种生物治疗方法可常规用于EBA的治疗。