Ustekinumab: an evidence-based review of its effectiveness in the treatment of psoriasis.

Core Evidence Pub Date : 2010-07-27 DOI:10.2147/ce.s5994
Eliana Krulig, Kenneth B Gordon
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引用次数: 10

Abstract

Introduction: Psoriasis is a chronic inflammatory skin disease affecting approximately 2% to 3% of the population worldwide. Discoveries over the past 3 to 5 years have significantly altered our view of psoriasis as primarily a T-cell mediated condition. The most recent research has demonstrated the essential role of specific cytokines in the development of this complex disease, including TNF-alpha, interleukin-23 (IL-23), and potentially, IL-22. These are all part of a newly defined autoimmune pathway directed by specialized T cells called Th17 helper T cells. Ustekinumab is a fully human monoclonal antibody that targets IL-12 and IL-23, thus targeting both Th1 and Th17 arms of immunity. It has a promising efficacy and safety profile that not only represents a valuable treatment alternative, but also a continuation in our constantly evolving understanding of this disorder.

Aims: To review the emerging evidence supporting the use of ustekinumab in the management of moderate to severe plaque psoriasis.

Evidence review: There is clear evidence that ustekinumab is effective in the treatment of moderate to severe psoriasis. Phase III trials (PHOENIX 1 and 2) demonstrated a statistically significant difference between Psoriasis Area and Severity Index (PASI) 75 responses achieved by patients receiving ustekinumab, given as a 45 mg or 90 mg subcutaneous injection every 12 weeks, than their placebo counterparts. Treatment with this novel agent resulted in a rapid onset of action, with over 60% of treated patients attaining Physician's Global Assessment (PGA) scores of "cleared" or "minimal" by week 12. Quality of life assessments paralleled clinical improvements.

Clinical potential: Ustekinumab is an effective and efficient therapeutic option for patients with moderate to severe psoriasis. Although further studies are required to establish ustekinumab's place in the therapy of psoriasis, with its convenient dosing schedule and rapid onset of action, this drug could provide a great addition to the current therapeutic armamentarium available for psoriatic patients.

Abstract Image

Ustekinumab:对其治疗牛皮癣有效性的循证评价。
牛皮癣是一种慢性炎症性皮肤病,影响全球约2%至3%的人口。过去3到5年的发现显著改变了我们认为牛皮癣主要是一种t细胞介导的疾病的观点。最近的研究表明,特定细胞因子在这种复杂疾病的发展中起着重要作用,包括tnf - α、白细胞介素-23 (IL-23)和潜在的IL-22。这些都是新定义的自身免疫途径的一部分,由称为Th17辅助性T细胞的特殊T细胞指导。Ustekinumab是一种全人源单克隆抗体,靶向IL-12和IL-23,从而同时靶向免疫系统的Th1和Th17分支。它具有良好的疗效和安全性,不仅代表了一种有价值的治疗选择,而且是我们对这种疾病不断发展的理解的延续。目的:回顾支持使用ustekinumab治疗中度至重度斑块型银屑病的新证据。证据回顾:有明确的证据表明,ustekinumab对治疗中度至重度牛皮癣有效。III期试验(PHOENIX 1和PHOENIX 2)显示,接受ustekinumab治疗的患者,每12周皮下注射45 mg或90 mg,与安慰剂治疗的患者相比,银屑病面积和严重程度指数(PASI) 75的疗效有统计学显著差异。使用这种新型药物治疗导致快速起效,超过60%的治疗患者在第12周达到医师整体评估(PGA)评分“清除”或“最低”。生活质量评估与临床改善相一致。临床潜力:Ustekinumab是中度至重度牛皮癣患者的有效治疗选择。虽然还需要进一步的研究来确定ustekinumab在银屑病治疗中的地位,但由于其方便的给药计划和快速的起效,该药物可以为银屑病患者提供目前可用的治疗方案。
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来源期刊
Core Evidence
Core Evidence PHARMACOLOGY & PHARMACY-
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期刊介绍: Core Evidence evaluates the evidence underlying the potential place in therapy of drugs throughout their development lifecycle from preclinical to postlaunch. The focus of each review is to evaluate the case for a new drug or class in outcome terms in specific indications and patient groups The emerging evidence on new drugs is reviewed at key stages of development and evaluated against unmet needs
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