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本文引用的文献

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The long-term safety of adalimumab treatment in moderate to severe psoriasis: a comprehensive analysis of all adalimumab exposure in all clinical trials.阿达木单抗治疗中重度银屑病的长期安全性:所有临床试验中所有阿达木单抗暴露情况的综合分析。
Am J Clin Dermatol. 2011 Oct 1;12(5):321-37. doi: 10.2165/11587890-000000000-00000.
2
An open-label, prospective cohort pilot study to evaluate the efficacy and safety of etanercept in the treatment of moderate to severe plaque psoriasis in patients who have not had an adequate response to adalimumab.一项开放标签的前瞻性队列先导研究,旨在评估依那西普在治疗对阿达木单抗反应欠佳的中度至重度斑块状银屑病患者中的疗效和安全性。
J Drugs Dermatol. 2011 Apr;10(4):396-402.
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Safety of treatment with biologics for psoriasis in daily practice: 5-year data.生物制剂治疗银屑病的日常实践安全性:5 年数据。
J Eur Acad Dermatol Venereol. 2012 Mar;26(3):283-91. doi: 10.1111/j.1468-3083.2011.04044.x. Epub 2011 Mar 24.
4
Efficacy and safety of adalimumab among patients with moderate to severe psoriasis with co-morbidities: Subanalysis of results from a randomized, double-blind, placebo-controlled, phase III trial.伴有合并症的中重度银屑病患者使用阿达木单抗的疗效和安全性:一项随机、双盲、安慰剂对照、III 期临床试验的结果亚组分析。
Am J Clin Dermatol. 2011 Feb 1;12(1):51-62. doi: 10.2165/11530640-000000000-00000.
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Switching biologics for psoriasis.更换治疗银屑病的生物制剂。
Br J Dermatol. 2010 Oct;163(4):667-9. doi: 10.1111/j.1365-2133.2010.09999.x.
6
Adalimumab for psoriasis: practical experience in a U.K. tertiary referral centre.阿达木单抗治疗银屑病:英国三级转诊中心的实践经验。
Br J Dermatol. 2010 Oct;163(4):859-62. doi: 10.1111/j.1365-2133.2010.09986.x.
7
Switching from etanercept to adalimumab is effective and safe: results in 30 patients with psoriasis with primary failure, secondary failure or intolerance to etanercept.从依那西普转换至阿达木单抗是有效且安全的:结果显示在 30 例对依那西普原发性失效、继发性失效或不耐受的银屑病患者中。
Br J Dermatol. 2010 Oct;163(4):838-46. doi: 10.1111/j.1365-2133.2010.09950.x. Epub 2010 Sep 2.
8
Extent and clinical consequences of antibody formation against adalimumab in patients with plaque psoriasis.斑块状银屑病患者中抗阿达木单抗抗体形成的程度及临床后果。
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9
Treatment of psoriasis in patients with hepatitis C: from the Medical Board of the National Psoriasis Foundation.丙型肝炎患者银屑病的治疗:来自美国国家银屑病基金会医学委员会
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10
Adalimumab safety and mortality rates from global clinical trials of six immune-mediated inflammatory diseases.阿达木单抗在六种免疫介导的炎症性疾病全球临床试验中的安全性和死亡率。
Ann Rheum Dis. 2009 Dec;68(12):1863-9. doi: 10.1136/ard.2008.102103. Epub 2009 Jan 15.

抗TNFα疗法在银屑病治疗中的应用:一家国家级转诊中心的经验

Anti-TNFα therapy in the management of psoriasis: experience of a state referral center.

作者信息

Silva Laura Maria Andrade, Rocha Bruno de Oliveira, Nobre Ana Cláudia Pinto, Rêgo Vitória Regina Pedreira de Almeida, Follador Ivonise, Oliveira Maria de Fátima Santos Paim de

机构信息

Universidade Federal da Bahia, Salvador, BA, Brazil.

出版信息

An Bras Dermatol. 2014 May-Jun;89(3):436-40. doi: 10.1590/abd1806-4841.20142613.

DOI:10.1590/abd1806-4841.20142613
PMID:24937817
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4056701/
Abstract

BACKGROUND

Psoriasis is a chronic immune-mediated disease, characterized by increased levels of TNFα. Anti-TNFα agents have revolutionized the treatment of severe psoriasis by targeting an important molecule involved in its pathogenesis.

OBJECTIVES

We report the experience of a state referral center that uses anti-TNFα agents for psoriasis.

METHODS

We conducted a retrospective case series. Seventy-four out of 120 patients met the inclusion criteria. Clinical and laboratory data was analyzed using the chi-squared, Wicoxon and McNemar's tests. Associations were considered statistically significant when p-value<0.05.

RESULTS

Forty-one subjects (55.40%) were male, with a mean age of 47.69 ± 14.99 years. Median disease duration and pre-treatment PASI were 14.0 months (IQR 9.0-20.0), and 13.55 points (IQR 8.5-20.32). Sixty patients (81.10%) had arthropathic psoriasis. Forty-six subjects (62.20%) had comorbidities; the most frequent was dyslipidemia (25.70%). In 55.40% of patients, insufficient response to conventional therapies was the principal indication for using anti-TNFα drugs. Clinical improvement occurred in 93.20% of cases, and the post-treatment PASI median was 0.0 points (IQR 0.0-0.0). Adverse effects occurred in 6.80% of patients. Infections and elevation of transaminases occurred in 28.40% and 8.10% of cases, respectively.

CONCLUSION

Post-treatment reduction in PASI was satisfactory and the occurrence of adverse effects was minor, mostly mild infusion effects and local reactions at drug administration sites.

摘要

背景

银屑病是一种慢性免疫介导性疾病,其特征为肿瘤坏死因子α(TNFα)水平升高。抗TNFα药物通过靶向参与其发病机制的重要分子,彻底改变了重度银屑病的治疗方式。

目的

我们报告一家国家转诊中心使用抗TNFα药物治疗银屑病的经验。

方法

我们进行了一项回顾性病例系列研究。120例患者中有74例符合纳入标准。使用卡方检验、 Wilcoxon检验和McNemar检验对临床和实验室数据进行分析。当p值<0.05时,关联被认为具有统计学意义。

结果

41名受试者(55.40%)为男性,平均年龄为47.69±14.99岁。疾病持续时间中位数和治疗前银屑病面积和严重程度指数(PASI)分别为14.0个月(四分位间距9.0 - 20.0)和13.55分(四分位间距8.5 - 20.32)。60例患者(81.10%)患有关节病型银屑病。46名受试者(62.20%)有合并症;最常见的是血脂异常(25.70%)。在55.40%的患者中,对传统疗法反应不足是使用抗TNFα药物的主要指征。93.20%的病例出现临床改善,治疗后PASI中位数为0.0分(四分位间距0.0 - 0.0)。6.80%的患者出现不良反应。感染和转氨酶升高分别发生在28.40%和8.10%的病例中。

结论

治疗后PASI降低情况令人满意,不良反应发生率较低,主要为轻度输注反应和给药部位局部反应。