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肌肉内注射阿法赛普特治疗慢性斑块状银屑病的多次疗程的安全性概况及持续缓解情况。

The safety profile and sustained remission associated with response to multiple courses of intramuscular alefacept for treatment of chronic plaque psoriasis.

机构信息

Northwest Dermatology and Research Center, Portland, Oregon, USA.

出版信息

J Am Acad Dermatol. 2010 Jun;62(6):968-78. doi: 10.1016/j.jaad.2009.07.032. Epub 2010 Apr 14.

Abstract

BACKGROUND

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.

OBJECTIVE

We sought to determine the safety and efficacy of up to 5 courses of alefacept IM in treating plaque psoriasis.

METHODS

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.

RESULTS

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.

LIMITATIONS

This was an extension study and therefore contained no control group.

CONCLUSIONS

Up to 5 courses of alefacept IM may provide extended treatment-free, symptom-free periods in responders while maintaining the safety profile.

摘要

背景

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。

目的

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。

方法

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。

结果

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。

局限性

这是一项扩展研究,因此没有对照组。

结论

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。

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