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沙特阿拉伯一项回顾性队列研究:银屑病管理中生物疗法的处方模式和持续性。

Prescribing patterns and persistence of biological therapies for psoriasis management: a retrospective cohort study from Saudi Arabia.

机构信息

Department of Clinical Pharmacy, Prince Sattam Bin Abdulaziz University, Alkharj, Saudi Arabia.

Pharmaceutical Care Services, Eastern Health Cluster, Dammam, Saudi Arabia.

出版信息

J Dermatolog Treat. 2024 Dec;35(1):2386973. doi: 10.1080/09546634.2024.2386973. Epub 2024 Aug 5.

Abstract

BACKGROUND

Biological therapies are effective for psoriasis, but patient responses vary, often requiring therapy switching or discontinuation.

OBJECTIVES

To identify physicians' prescribing patterns of biological therapies at a referral tertiary center in Saudi Arabia and assess the probability of biologic persistence following treatment initiation.

METHODS

We conducted a retrospective study of biologic-naïve adult psoriasis patients who initiated therapy from October 2013 to July 2022 in Dammam. Descriptive statistics and a Kaplan-Meier analysis evaluated treatment persistence at 6, 12, 24, and 36 months.

RESULTS

A total of 151 patients received adalimumab ( = 89), etanercept ( = 17), risankizumab ( = 30), ustekinumab ( = 14), and ixekizumab ( = 1). At 6 months, all therapies demonstrated 100% persistence. At 12 months, persistence was highest for ustekinumab (100%) and lowest for etanercept (88.2%). At 24 months, ustekinumab maintained 100% persistence, followed by risankizumab (96.6%), adalimumab (94.3%), and etanercept (76.4%). At 36 months, risankizumab had the highest persistence (96.6%), followed by adalimumab (83.1%), ustekinumab (78%), and etanercept (70.6%). The most common reasons for discontinuation were lack of effectiveness and intolerability.

CONCLUSION

This study shows changing psoriasis treatment patterns with new therapies. Risankizumab demonstrated high long-term persistence, while etanercept and ustekinumab showed declining persistence, suggesting evolving treatment considerations.

摘要

背景

生物疗法对银屑病有效,但患者的反应各不相同,通常需要转换或停止治疗。

目的

在沙特阿拉伯的一家转诊三级中心确定医生对生物疗法的处方模式,并评估治疗开始后生物制剂持续存在的概率。

方法

我们对 2013 年 10 月至 2022 年 7 月在达曼接受生物治疗的初治成人银屑病患者进行了回顾性研究。描述性统计和 Kaplan-Meier 分析评估了治疗开始后 6、12、24 和 36 个月的治疗持续时间。

结果

共有 151 名患者接受了阿达木单抗(89 名)、依那西普(17 名)、里司奴单抗(30 名)、乌司奴单抗(14 名)和依奇珠单抗(1 名)治疗。在 6 个月时,所有治疗方法的持续率均为 100%。在 12 个月时,乌司奴单抗的持续率最高(100%),依那西普的持续率最低(88.2%)。在 24 个月时,乌司奴单抗保持 100%的持续率,其次是里司奴单抗(96.6%)、阿达木单抗(94.3%)和依那西普(76.4%)。在 36 个月时,里司奴单抗的持续率最高(96.6%),其次是阿达木单抗(83.1%)、乌司奴单抗(78%)和依那西普(70.6%)。停药的最常见原因是无效和不耐受。

结论

本研究显示随着新疗法的出现,银屑病的治疗模式发生了变化。里司奴单抗显示出较高的长期持续率,而依那西普和乌司奴单抗的持续率则呈下降趋势,这表明治疗考虑因素在不断演变。

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