Northwest Dermatology and Research Center, Portland, Oregon, USA.
J Am Acad Dermatol. 2010 Jun;62(6):968-78. doi: 10.1016/j.jaad.2009.07.032. Epub 2010 Apr 14.
Safety and efficacy of up to 3 courses of alefacept intramuscular (IM) in the treatment of chronic plaque psoriasis have been demonstrated in earlier trials.
We sought to determine the safety and efficacy of up to 5 courses of alefacept IM in treating plaque psoriasis.
A standard treatment course was defined as 15 mg of alefacept IM once weekly for 12 weeks, followed by 12 weeks of treatment-free observation. Patients with chronic plaque psoriasis, who had previously received alefacept IM, received up to 3 additional courses (A, B, and C). Efficacy was evaluated by Physician Global Assessment.
Safety profiles were similar to those for a single course of treatment. There were no cumulative adverse effects. At 2 weeks postdosing, 16%, 22%, and 19% of patients were rated clear or almost clear by Physician Global Assessment in courses A, B, and C, respectively, with 35%, 42%, and 42% achieving this response at any time during these courses. Patients who achieved clear or almost clear at 2 weeks postdosing remained so for a median duration of 214 and 126 days after courses A and B, respectively.
This was an extension study and therefore contained no control group.
Up to 5 courses of alefacept IM may provide extended treatment-free, symptom-free periods in responders while maintaining the safety profile.
在早期试验中,已证实多达 3 个疗程的阿法赛普特肌内注射(IM)治疗慢性斑块状银屑病的安全性和有效性。
我们旨在确定多达 5 个疗程的阿法赛普特 IM 治疗斑块状银屑病的安全性和有效性。
一个标准疗程定义为每周一次给予 15 毫克阿法赛普特 IM,共 12 周,然后进行 12 周的无治疗观察期。先前接受过阿法赛普特 IM 治疗的慢性斑块状银屑病患者接受多达 3 个额外疗程(A、B 和 C)。通过医生总体评估来评估疗效。
安全性与单一疗程相似。没有累积的不良反应。在给药后 2 周,A、B 和 C 疗程中分别有 16%、22%和 19%的患者被医生总体评估评为清除或几乎清除,在这些疗程的任何时间,有 35%、42%和 42%的患者达到此反应。在给药后 2 周达到清除或几乎清除的患者,在 A 疗程和 B 疗程后分别有 214 天和 126 天的中位持续时间保持如此状态。
这是一项扩展研究,因此没有对照组。
多达 5 个疗程的阿法赛普特 IM 可能为应答者提供延长的无治疗、无症状期,同时保持安全性。