A multicenter, randomized, open-label pilot trial assessing the efficacy and safety of etanercept 50 mg twice weekly followed by etanercept 25 mg twice weekly, the combination of etanercept 25 mg twice weekly and acitretin, and acitretin alone in patients with moderate to severe psoriasis.

Q2 Medicine BMC Dermatology Pub Date : 2016-07-25 DOI:10.1186/s12895-016-0048-z
Joo-Heung Lee, Jai-Il Youn, Tae-Yoon Kim, Jee-Ho Choi, Chul-Jong Park, Yong-Beom Choe, Hae-Jun Song, Nack-In Kim, Kwang-Joong Kim, Jeung-Hoon Lee, Hyun-Jeong Yoo
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Abstract

Background: Etanercept, a soluble tumor necrosis factor receptor, and acitretin have been shown to be effective in treating psoriasis. Acitretin is widely used in Korea. However, the combination of etanercept plus acitretin has not been evaluated among Korean patients with psoriasis. The objective of this study was to investigate the efficacy and safety of combination therapy with etanercept and acitretin in patients with moderate to severe plaque psoriasis.

Methods: Sixty patients with psoriasis were randomized to receive etanercept 50 mg twice weekly (BIW) for 12 weeks followed by etanercept 25 mg BIW for 12 weeks (ETN-ETN); etanercept 25 mg BIW plus acitretin 10 mg twice daily (BID) for 24 weeks (ETN-ACT); or acitretin 10 mg BID for 24 weeks (ACT). The primary efficacy measurement was the proportion of patients achieving 75 % improvement in Psoriasis Area and Severity Index (PASI 75) at week 24. Secondary end points included 50 % improvement in PASI (PASI 50) at week 24 and clear/almost-clear by Physician Global Assessment (PGA) at each visit through week 24.

Results: The proportions of patients achieving PASI 75, PASI 50, and PGA clear/almost-clear at week 24 in the ETN-ETN (52.4, 71.4, and 52.4 %, respectively) and ETN-ACT groups (57.9, 84.2, and 52.6 %, respectively) were higher than in the ACT group (22.2, 44.4, and 16.7 %, respectively). The incidence of adverse events was similar across all arms. This was an open-label study with a small number of patients.

Conclusion: In Korean patients with moderate to severe plaque psoriasis, etanercept alone or in combination with acitretin was more effective than acitretin. All treatments were well tolerated throughout the study.

Trial registration: This study was registered on July 7, 2009 at ClinicalTrials.gov, NCT00936065 .

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一项多中心、随机、开放标签的试点试验,评估依那西普50 mg每周2次,随后依那西普25 mg每周2次,依那西普25 mg每周2次与阿维甲素联合,以及单独使用阿维甲素治疗中重度牛皮癣患者的疗效和安全性。
背景:依那西普(一种可溶性肿瘤坏死因子受体)和阿维素已被证明对治疗牛皮癣有效。阿曲维素在韩国被广泛使用。然而,依那西普联合阿维甲素在韩国银屑病患者中尚未进行评估。本研究的目的是探讨依那西普和阿维甲素联合治疗中重度斑块型银屑病的疗效和安全性。方法:60例银屑病患者随机接受依那西普50 mg,每周2次(BIW),连续12周,随后接受依那西普25 mg,每周2次(ETN-ETN);依那普25mg BIW加阿维素10mg,每日两次(BID),持续24周(ETN-ACT);或活塞素10mg BID, 24周(ACT)。主要疗效测量是第24周时银屑病面积和严重程度指数(PASI 75)改善75%的患者比例。次要终点包括第24周时PASI改善50% (PASI 50),第24周每次就诊时医师总体评估(PGA)清除/几乎清除。结果:在第24周,ETN-ETN组(分别为52.4、71.4和52.4%)和ETN-ACT组(分别为57.9、84.2和52.6%)达到PASI 75、PASI 50和PGA清除/几乎清除的患者比例高于ACT组(分别为22.2、44.4和16.7%)。所有组的不良事件发生率相似。这是一项少数患者的开放标签研究。结论:在韩国中重度斑块型银屑病患者中,依那西普单用或联用阿维甲素比阿维甲素更有效。在整个研究过程中,所有治疗方法均具有良好的耐受性。试验注册:本研究于2009年7月7日在ClinicalTrials.gov注册,注册号为NCT00936065。
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BMC Dermatology
BMC Dermatology Medicine-Dermatology
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期刊介绍: BMC Dermatology is an open access journal publishing original peer-reviewed research articles in all aspects of the prevention, diagnosis and management of skin disorders, as well as related molecular genetics, pathophysiology, and epidemiology. BMC Dermatology (ISSN 1471-5945) is indexed/tracked/covered by PubMed, MEDLINE, CAS, EMBASE, Scopus and Google Scholar.
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