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制定中重度银屑病管理循证策略的尝试:生物制剂和生物前体药物选项的疗效与安全性综述

An attempt to formulate an evidence-based strategy in the management of moderate-to-severe psoriasis: a review of the efficacy and safety of biologics and prebiologic options.

作者信息

Leon Argentina, Nguyen Alain, Letsinger Julie, Koo John

机构信息

University of Miami, Miller School of Medicine, Miami, FL, USA.

出版信息

Expert Opin Pharmacother. 2007 Apr;8(5):617-32. doi: 10.1517/14656566.8.5.617.

DOI:10.1517/14656566.8.5.617
PMID:17376017
Abstract

Psoriasis is a chronic skin disorder affecting up to 2.5% of the world's population. Despite the myriad treatment options available, there is no uniformly accepted therapeutic approach for moderate-to-severe psoriasis. The objective of this review is to evaluate the relative efficacy and safety of available therapeutic options and to formulate general recommendations for the treatment of moderate-to-severe psoriasis. MEDLINE and Evidence Based Medicine (Cochrane) were used to perform a comprehensive search of the literature from 1986 to 2006. The most scientifically rigorous clinical trial published in the literature was selected for Psoriasis Area and Severity Index (PASI 75) comparison. Only information from clinical trials, human subjects and English language journals are reported in this study. The percentage of PASI 75 reduction at approximately 12 weeks obtained by the following treatment options were: Goeckerman and RePUVA, 100%; calcipotriene plus PUVA, 87%; ciclosporin, 78.2-80.3%; infliximab, 80%; adalimumab 40 mg every other week, 53% and 40 mg/week, 80%; PUVA, 63%; methotrexate, 60%; NB-UVB, 55%; acitretin 52%; etanercept 50 mg twice weekly, 49% and 25 mg twice weekly, 34%; efalizumab, 31.4%; and alefacept 21%. Psoriatic treatments with safer profiles compared with other agents include bath PUVA, Goeckerman and RePUVA. Based on the literature review of efficacy and safety of biologics and prebiologic treatment options for moderate-to-severe psoriasis, the risk:benefit ratio seems most favorable for Goeckerman and RePUVA, followed by either etanercept or adalimumab.

摘要

银屑病是一种慢性皮肤疾病,影响着全球多达2.5%的人口。尽管有众多可用的治疗选择,但对于中度至重度银屑病,尚无统一接受的治疗方法。本综述的目的是评估现有治疗选择的相对疗效和安全性,并为中度至重度银屑病的治疗制定一般性建议。使用MEDLINE和循证医学(Cochrane)对1986年至2006年的文献进行全面检索。选择文献中发表的最具科学严谨性的临床试验进行银屑病面积和严重程度指数(PASI 75)比较。本研究仅报告来自临床试验、人体受试者和英文期刊的信息。以下治疗选择在大约12周时获得的PASI 75降低百分比为:Goeckerman疗法和补骨脂素-紫外线A联合疗法(RePUVA)为100%;卡泊三醇加补骨脂素-紫外线A联合疗法为87%;环孢素为78.2 - 80.3%;英夫利昔单抗为80%;阿达木单抗每隔一周40mg为53%,每周40mg为80%;补骨脂素-紫外线A联合疗法为63%;甲氨蝶呤为60%;窄谱中波紫外线(NB-UVB)为55%;阿维A为52%;依那西普每周两次50mg为49%,每周两次25mg为34%;依法利珠单抗为31.4%;阿法赛特为21%。与其他药物相比,安全性更高的银屑病治疗方法包括浴用补骨脂素-紫外线A联合疗法、Goeckerman疗法和RePUVA。基于对中度至重度银屑病生物制剂和生物前体治疗选择的疗效和安全性的文献综述,风险效益比似乎对Goeckerman疗法和RePUVA最为有利,其次是依那西普或阿达木单抗。

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