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布罗达单抗治疗银屑病的疗效及治疗失败的危险因素:一项事后分析综述

Efficacy of Brodalumab in Patients with Psoriasis and Risk Factors for Treatment Failure: A Review of Post Hoc Analyses.

作者信息

Lebwohl Mark G, Armstrong April W, Alexis Andrew F, Lain Edward L, Jacobson Abby A

机构信息

Icahn School of Medicine at Mount Sinai, 5 East 98 Street, 5 Floor, New York, NY, 10029, USA.

University of California, Los Angeles, CA, USA.

出版信息

Dermatol Ther (Heidelb). 2024 Oct;14(10):2709-2726. doi: 10.1007/s13555-024-01264-3. Epub 2024 Sep 12.

Abstract

Factors such as obesity, alcohol consumption, and tobacco use are associated with both increased psoriasis severity and inadequate response to systemic and biologic therapies. Obesity is linked to chronic inflammation, which can contribute to psoriasis pathogenesis. Fixed-dose therapies may have reduced efficacy in patients with a higher body mass index, while weight-based dosing can increase the burden of drug-specific side effects. Alcohol and nicotine from tobacco have also been shown to stimulate keratinocyte and immune cell proliferation and production of proinflammatory cytokines. While these risk factors are prevalent among patients with moderate-to-severe psoriasis, their influence on treatment outcomes may be overlooked when evaluating therapeutic options. Brodalumab is a fully human interleukin-17 receptor A antagonist approved for the treatment of moderate-to-severe psoriasis. In this review, we describe the lifestyle-related risk factors associated with decreased response to treatment. We further summarize the post hoc analyses of brodalumab in participant subgroups with moderate-to-severe psoriasis and a history of prior biologic failure, obesity, and alcohol or tobacco use from two phase 3 clinical trials (AMAGINE-2 and AMAGINE-3; ClinicalTrials.gov identifiers: NCT01708603 and NCT01708629, respectively). Our review of clinical trial and real-world data suggests that brodalumab is an efficacious and safe treatment option for patients with lifestyle factors that increase the likelihood of treatment failure, allowing them to achieve skin clearance and improve quality of life.

摘要

肥胖、饮酒和吸烟等因素与银屑病严重程度增加以及对全身治疗和生物治疗反应不足有关。肥胖与慢性炎症相关,这可能促使银屑病发病。固定剂量疗法对体重指数较高的患者疗效可能降低,而基于体重的给药方式会增加特定药物副作用的负担。烟草中的酒精和尼古丁也已被证明可刺激角质形成细胞和免疫细胞增殖以及促炎细胞因子的产生。虽然这些风险因素在中度至重度银屑病患者中普遍存在,但在评估治疗方案时,它们对治疗结果的影响可能被忽视。布罗达单抗是一种全人源白细胞介素 -17 受体 A 拮抗剂,被批准用于治疗中度至重度银屑病。在本综述中,我们描述了与治疗反应降低相关的生活方式相关风险因素。我们进一步总结了来自两项 3 期临床试验(AMAGINE - 2 和 AMAGINE - 3;ClinicalTrials.gov 标识符分别为 NCT01708603 和 NCT01708629)中,针对有中度至重度银屑病病史且有既往生物制剂治疗失败、肥胖以及有饮酒或吸烟史的参与者亚组进行的布罗达单抗事后分析。我们对临床试验和真实世界数据的综述表明,对于存在增加治疗失败可能性的生活方式因素的患者,布罗达单抗是一种有效且安全的治疗选择,可使他们实现皮肤清除并改善生活质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05b3/11480272/2f97a3d86287/13555_2024_1264_Fig1_HTML.jpg

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