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首页> 外文期刊>The Journal of dermatological treatment >Psoriasis responds to intralesional injections of alefacept and may predict systemic response to intramuscular alefacept: Interim results of a single-arm, open-label study
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Psoriasis responds to intralesional injections of alefacept and may predict systemic response to intramuscular alefacept: Interim results of a single-arm, open-label study

机译:牛皮癣对病灶内注射alefacept有反应,并可预测对肌内alefacept的全身反应:单臂,开放标签研究的中期结果

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Background: Alefacept is a remittive treatment for generalized psoriasis but is rarely used due to its erratic efficacy. Objective: To determine if psoriasis plaques will respond to intralesional alefacept and if this predicts a systemic response to intramuscular (IM) alefacept. Methods: We describe a 25-week, single-center, open-label study. Patients received weekly intralesional alefacept of increasing concentrations into target plaques for 3 weeks followed by IM injections for 12 weeks and concluded with an observation period of 9 weeks. The psoriasis area and severity index (PASI) was used to assess the efficacy of IM alefacept. Results: Interim results are reported for the first seven patients enrolled. Two patients responded intralesionally to the most dilute 1:100 concentration of alefacept to sterile water and achieved a 59% and 100% improvement in PASI. Five patients did not respond intralesionally to the most dilute form of alefacept and none achieved PASI 75. Two of these five patients did not respond to any concentration and achieved a 26% and 38% improvement in PASI. Limitations to this study include a small sample size and being non-placebo-controlled. Conclusion: Alefacept is effective intralesionally and may predict a systemic response challenging the concept that biologics must work systemically.
机译:背景:Alefacept是一种治疗性牛皮癣的治疗方法,但由于疗效不稳定而很少使用。目的:确定牛皮癣斑块是否会对病灶内alefacept作出反应,以及这是否预测对肌内alefacept的全身反应。方法:我们描述了一项为期25周的单中心开放标签研究。患者每周接受病灶内alefacept增加浓度进入目标斑块3周,然后IM注射12周,观察期为9周。牛皮癣面积和严重程度指数(PASI)用于评估IM alefacept的疗效。结果:报道了前7名患者的中期结果。两名患者对无菌水中最稀的1:100 alefacept浓度发生病灶内反应,PASI改善了59%和100%。五名患者对最稀薄的alefacept病灶内无反应,均未达到PASI75。这五名患者中有两名对任何浓度均无反应,PASI改善了26%和38%。该研究的局限性包括样本量小且不受安慰剂控制。结论:Alefacept在病变内有效,并可预测全身反应,这挑战了生物制剂必须全身起作用的观念。

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