Reich Kristian, Thaci Diamant, Mrowietz Ulrich, Kamps Anja, Neureither Marcus, Luger Thomas
Dermatologikum Hamburg, Hamburg, Germany.
J Dtsch Dermatol Ges. 2009 Jul;7(7):603-11. doi: 10.1111/j.1610-0387.2009.07120.x. Epub 2009 May 4.
This study collected data on the safety and efficacy of fumaric acid esters (FAE; Fumaderm) in the long-term treatment of psoriasis.
Patients were included at 163 dermatological centers if they either had been treated continuously with FAE for at least 24 months, or for 36 months with interruptions of no longer than 6 months. Data were reported from baseline, after 3, 6, 12, 24, and 36 or more months of therapy. Safety parameters were monitored and the severity of skin symptoms was assessed by "Physician's Global Assessment" (PGA) and "Psoriasis Area and Severity Index" (PASI).
984 patients were included with a mean duration of 44 months of continuous treatment. The percentage of patients documented as markedly improved or clear was 67 % after six months, 78 % after 24 months, and 82 % after 36 months of therapy. Improvement was similar in patients with moderate and severe disease. Changes of laboratory parameters were usually insignificant and did not require a modification of FAE treatment in more than 90 % of the cases.
In the long-term treatment of patients with moderate and severe psoriasis FAE show a good and sustained clinical efficacy combined with a favorable safety profile.
本研究收集了富马酸酯(FAE;商品名Fumaderm)长期治疗银屑病的安全性和有效性数据。
如果患者连续接受FAE治疗至少24个月,或接受治疗36个月且中断时间不超过6个月,则纳入163个皮肤科中心。报告了治疗基线、治疗3、6、12、24以及36个月及以上后的各项数据。监测安全性参数,并通过“医生整体评估”(PGA)和“银屑病面积和严重程度指数”(PASI)评估皮肤症状的严重程度。
共纳入984例患者,平均持续治疗时间为44个月。治疗6个月后,记录为显著改善或皮损清除的患者比例为67%,24个月后为78%,36个月后为82%。中度和重度疾病患者的改善情况相似。超过90%的病例中,实验室参数变化通常不显著,无需调整FAE治疗方案。
在中度和重度银屑病患者的长期治疗中,FAE显示出良好且持续的临床疗效,同时安全性良好。