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将系统性维甲酸与生物制剂联合用于中重度银屑病。

Combining systemic retinoids with biologic agents for moderate to severe psoriasis.

作者信息

Smith Elizabeth C A, Riddle Christy, Menter M Alan, Lebwohl Mark

机构信息

Department of Dermatology, Mount Sinai School of Medicine, New York, USA.

出版信息

Int J Dermatol. 2008 May;47(5):514-8. doi: 10.1111/j.1365-4632.2008.03470.x.

Abstract

BACKGROUND

Moderate to severe psoriasis, which is defined as psoriasis affecting more than 20% of the body surface area, often requires a combination of therapies to achieve remission. Although numerous data exist regarding the use of acitretin and biologic agent therapy alone for psoriasis, little is known about the efficacy, safety, and tolerability of acitretin combined with biologic agents.

METHODS

Fifteen patients with psoriasis treated with concomitant acitretin and a biologic agent were identified, and their charts were reviewed for response to therapy, additional therapy necessary for disease management, side-effects, and laboratory abnormalities whilst on combination therapy. The Institutional Review Board did not require approval for this chart review.

RESULTS

Twenty-nine per cent of patients showed clearance of psoriasis, 43% of patients showed an improvement of 90%, 14% showed an improvement of 75%, and 7.1% showed no change. During treatment with acitretin and biologic agent, five patients required no adjunctive treatment. Three patients were able to stop narrow-band ultraviolet-B (UV-B) therapy after an average of 2.33 months of combination therapy. Only one patient continued to require phototherapy (UV-B) in addition to the biologic agent. Three patients developed squamous cell carcinoma (SCC) whilst on combination therapy, but all patients had a previous history of SCC. One patient developed non-Hodgkin's lymphoma after 3 years of etanercept and acitretin, and the etanercept was discontinued.

CONCLUSIONS

Acitretin combined with biologic agents offers a promising method of managing refractory psoriasis. More research is needed to determine the long-term safety and efficacy of this combination.

摘要

背景

中度至重度银屑病定义为累及身体表面积超过20%的银屑病,通常需要联合多种疗法才能实现病情缓解。尽管已有大量关于单独使用阿维A和生物制剂治疗银屑病的数据,但对于阿维A联合生物制剂的疗效、安全性和耐受性知之甚少。

方法

确定了15例同时接受阿维A和生物制剂治疗的银屑病患者,并查阅了他们的病历,以了解治疗反应、疾病管理所需的额外治疗、副作用以及联合治疗期间的实验室异常情况。机构审查委员会不需要批准此次病历审查。

结果

29%的患者银屑病症状清除,43%的患者改善了90%,14%的患者改善了75%,7.1%的患者无变化。在阿维A和生物制剂治疗期间,5例患者无需辅助治疗。3例患者在联合治疗平均2.33个月后能够停止窄谱中波紫外线(UV-B)治疗。只有1例患者除生物制剂外仍需继续接受光疗(UV-B)。3例患者在联合治疗期间发生了鳞状细胞癌(SCC),但所有患者既往均有SCC病史。1例患者在接受依那西普和阿维A治疗3年后发生了非霍奇金淋巴瘤,随后停用了依那西普。

结论

阿维A联合生物制剂为治疗难治性银屑病提供了一种有前景的方法。需要更多研究来确定这种联合治疗的长期安全性和疗效。

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