Balak Deepak Mw
Department of Dermatology, Erasmus Medical Center, Rotterdam, the Netherlands.
Psoriasis (Auckl). 2015 Jan 5;5:9-23. doi: 10.2147/PTT.S51490. eCollection 2015.
Fumaric acid esters (FAE) are small molecules with immunomodulating, anti-inflammatory, and anti-oxidative effects. FAE were introduced as a systemic psoriasis treatment in 1959 and empirically developed further between 1970 and 1990 in Germany, Switzerland, and the Netherlands. The development of FAE as psoriasis treatment did not follow the traditional drug development phases. Nonetheless, in 1994 FAE were approved in Germany for the treatment of severe plaque psoriasis. FAE are currently one of the most commonly used treatments in Germany, and FAE are increasingly being used as an unlicensed treatment in several other European countries. To date, six randomized controlled trials and 29 observational studies have evaluated FAE in a combined total of 3,439 patients. The efficacy and safety profile of FAE is favorable. About 50%-70% of patients achieve at least 75% improvement in psoriasis severity after 16 weeks of treatment. Common adverse events of FAE include gastrointestinal complaints and flushing symptoms, which lead to treatment discontinuation in up to 40% of patients. Lymphocytopenia, eosinophilia, and proteinuria are commonly observed during FAE treatment, but rarely require treatment discontinuation. The long-term safety profile of continuous FAE treatment is favorable without an increased risk for infections, malignancies, or other serious adverse events. There are no known drug-interactions for FAE. The 2009 European evidence-based S3-guidelines on psoriasis treatment recommend FAE and suggest it as a first-line systemic treatment for moderate-to-severe plaque psoriasis. This review is aimed to give an overview of FAE treatment in the management of psoriasis.
富马酸酯(FAE)是具有免疫调节、抗炎和抗氧化作用的小分子。1959年,FAE被引入作为银屑病的全身治疗药物,并于1970年至1990年期间在德国、瑞士和荷兰根据经验进一步研发。FAE作为银屑病治疗药物的研发并未遵循传统的药物研发阶段。尽管如此,1994年FAE在德国被批准用于治疗重度斑块状银屑病。目前,FAE是德国最常用的治疗药物之一,并且在其他几个欧洲国家越来越多地被用作未经许可的治疗药物。迄今为止,六项随机对照试验和29项观察性研究共对3439例患者评估了FAE。FAE的疗效和安全性良好。约50%-70%的患者在治疗16周后银屑病严重程度至少改善75%。FAE常见的不良事件包括胃肠道不适和潮红症状,高达40%的患者因此停药。在FAE治疗期间常见淋巴细胞减少、嗜酸性粒细胞增多和蛋白尿,但很少需要停药。持续使用FAE治疗的长期安全性良好,感染、恶性肿瘤或其他严重不良事件的风险没有增加。FAE不存在已知的药物相互作用。2009年欧洲基于证据的银屑病治疗S3指南推荐FAE,并建议将其作为中重度斑块状银屑病的一线全身治疗药物。本综述旨在概述FAE在银屑病治疗中的应用。