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在美国,接受优特克单抗及其他生物制剂治疗的银屑病患者的治疗中断风险。

Risk of Treatment Discontinuation among Patients with Psoriasis Initiated on Ustekinumab and Other Biologics in the USA.

作者信息

Pilon Dominic, Fitzgerald Timothy, Zhdanava Maryia, Teeple Amanda, Morrison Laura, Shah Aditi, Lefebvre Patrick

机构信息

Groupe d'Analyse, 1190 Avenue des Canadiens-de-Montréal, Suite 1500, Montréal, QC, H3B 0G7, Canada.

Janssen Scientific Affairs, LLC., Titusville, NJ, USA.

出版信息

Dermatol Ther (Heidelb). 2022 Apr;12(4):971-987. doi: 10.1007/s13555-022-00707-z. Epub 2022 Mar 19.

Abstract

INTRODUCTION

Biologics are a standard therapy for patients with moderate-to-severe psoriasis, yet treatment persistence is essential to achieve disease control. Compared with other biologics, ustekinumab has been associated with lower rates of discontinuation and better adherence among patients with psoriasis, but prior studies have included limited data from the period after approval of self-administration for ustekinumab. This study was conducted to assess discontinuation risk among patients with plaque psoriasis initiating ustekinumab or other biologics.

METHODS

Adults with psoriasis and one or more claim for ustekinumab, secukinumab, adalimumab, or ixekizumab were identified in Optum's de-identified Clinformatics Data Mart Database (1 January 2010 to 30 June 2019). Treatment discontinuation was defined as a gap in days of therapy supply based on (1) each drug's per-label frequency of administration (main analysis) or (2) > 90 days (sensitivity analysis). Differences in baseline characteristics between the ustekinumab and other cohorts were adjusted with entropy balancing. Risk of discontinuation was compared with Cox proportional hazard models.

RESULTS

Overall, 2230 patients were included in the ustekinumab cohort, with 1807 in the secukinumab, 4483 in the adalimumab, and 535 in the ixekizumab cohorts (mean age 49.0 years, 49.3% female for all cohorts). In the main analysis, risk of discontinuation for the ustekinumab cohort was 62.2% lower than for adalimumab, 46.4% lower than for secukinumab, and 43.8% lower than for ixekizumab cohorts (all p < 0.001). Sensitivity analyses revealed no significant differences between the ustekinumab and other cohorts.

CONCLUSIONS

Patients with psoriasis initiating ustekinumab had lower risk of treatment discontinuation compared with other biologics when discontinuation was based on each drug's per-label frequency of administration. This finding may help inform choice of biologic based on compliance.

摘要

引言

生物制剂是中重度银屑病患者的标准治疗方法,但治疗的持续性对于实现疾病控制至关重要。与其他生物制剂相比,乌司奴单抗与银屑病患者较低的停药率和更好的依从性相关,但先前的研究纳入的乌司奴单抗自我给药获批后时期的数据有限。本研究旨在评估开始使用乌司奴单抗或其他生物制剂的斑块状银屑病患者的停药风险。

方法

在Optum的去识别化临床信息数据集市数据库(2010年1月1日至2019年6月30日)中识别出患有银屑病且有一项或多项使用乌司奴单抗、司库奇尤单抗、阿达木单抗或依奇珠单抗记录的成年人。治疗中断定义为基于以下情况的治疗供应天数的间隔:(1)每种药物标签上的给药频率(主要分析)或(2)>90天(敏感性分析)。使用熵平衡法对乌司奴单抗组与其他组之间的基线特征差异进行调整。使用Cox比例风险模型比较停药风险。

结果

总体而言,乌司奴单抗组纳入2230例患者,司库奇尤单抗组1807例,阿达木单抗组4483例,依奇珠单抗组535例(所有组的平均年龄为49.0岁,女性占49.3%)。在主要分析中,乌司奴单抗组的停药风险比阿达木单抗组低62.2%,比司库奇尤单抗组低46.4%,比依奇珠单抗组低43.8%(所有p<0.001)。敏感性分析显示乌司奴单抗组与其他组之间无显著差异。

结论

当根据每种药物标签上的给药频率定义停药时,开始使用乌司奴单抗的银屑病患者与其他生物制剂相比,治疗中断风险较低。这一发现可能有助于根据依从性为生物制剂的选择提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04e8/9021356/e9f3ccaa3b4c/13555_2022_707_Fig1_HTML.jpg

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