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长期依那西普治疗中重度慢性斑块型银屑病患者:澳大利亚扩大准入项目的结果。

Long-term efalizumab therapy for patients with moderate-to-severe, chronic plaque psoriasis: results from an Australian expanded access program.

机构信息

Department of Medicine (Dermatology), The University of Melbourne, St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.

出版信息

Int J Dermatol. 2009 Dec;48(12):1376-84. doi: 10.1111/j.1365-4632.2009.04217.x.

DOI:10.1111/j.1365-4632.2009.04217.x
PMID:19930495
Abstract

BACKGROUND

Psoriasis is a chronic skin disease that can impact heavily on a patient's well-being. Efalizumab, a unique, targeted, biological therapy, has demonstrated efficacy in treating moderate-to-severe, chronic plaque psoriasis with <or=36 months of continuous therapy. The objective of this Extended Access Program (EAP) was to evaluate further the benefit of efalizumab as long-term therapy in a real-world clinical setting.

METHODS

After an initial conditioning dose of efalizumab (0.7 mg/kg subcutaneously), a weekly dose of efalizumab (1.0 mg/kg) was administered for <or=21 months. Patients with reduced Psoriasis Area and Severity Index (PASI) scores (>or=50%, or a score <or=8) at month 3 entered the long-term maintenance treatment period.

RESULTS

In total, 101 patients (>18 years) with severe plaque psoriasis enrolled on the EAP, of these 93 (92.1%) met all the inclusion criteria. After 3 months of treatment, 84/101 (83.2%) patients had evaluable data and entered the maintenance period. After 3 months, 57/84 (67.9%) patients had achieved PASI-50. Using an intent-to-treat analysis, after 21 months of treatment, PASI-75 and PASI-50 were achieved by 43/101 (42.6%) and 69/101 (68.3%) of patients, respectively. Efalizumab was generally well tolerated during the 21 months of continuous therapy.

CONCLUSION

Efalizumab, 1.0 mg/kg/week, is effective and well tolerated in a 'real world' clinical setting, providing enduring reduction of psoriasis symptoms for up to 21 months.

摘要

背景

银屑病是一种慢性皮肤病,会对患者的健康产生重大影响。依那西普是一种独特的、靶向的生物疗法,在接受连续 36 个月的治疗后,对中重度慢性斑块型银屑病具有疗效。本扩展准入项目(EAP)的目的是在现实临床环境中进一步评估依那西普作为长期治疗的益处。

方法

在依那西普初始诱导剂量(皮下 0.7mg/kg)后,每周给予依那西普(1.0mg/kg),持续治疗<或=21 个月。在第 3 个月时 PASI 评分(>或=50%,或评分<或=8)降低的患者进入长期维持治疗期。

结果

在 EAP 中,共有 101 例(>18 岁)严重斑块型银屑病患者入组,其中 93 例(92.1%)符合所有纳入标准。治疗 3 个月后,84/101(83.2%)例患者可评估数据并进入维持期。治疗 3 个月后,57/84(67.9%)例患者达到 PASI-50。采用意向治疗分析,治疗 21 个月后,43/101(42.6%)例和 69/101(68.3%)例患者分别达到 PASI-75 和 PASI-50。依那西普在连续 21 个月的治疗期间总体耐受性良好。

结论

依那西普,每周 1.0mg/kg,在“真实世界”临床环境中具有疗效和良好的耐受性,可提供长达 21 个月的持久缓解银屑病症状。

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Long-term efalizumab therapy for patients with moderate-to-severe, chronic plaque psoriasis: results from an Australian expanded access program.长期依那西普治疗中重度慢性斑块型银屑病患者:澳大利亚扩大准入项目的结果。
Int J Dermatol. 2009 Dec;48(12):1376-84. doi: 10.1111/j.1365-4632.2009.04217.x.
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Efalizumab in the treatment of psoriasis.依法利珠单抗治疗银屑病。
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