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银屑病中替拉珠单抗生存情况的真实世界研究:关节炎、高血压及既往生物制剂使用情况的影响

Real-World Study of Tildrakizumab Survival in Psoriasis: Impact of Arthritis, Hypertension, and Prior Biologic Use.

作者信息

Santos-Juanes Galache Raquel, Reyes García Sebastian, Carrero Martín Jimena, Nuñez Domínguez Álvaro, López Pando Marta, Álvarez Losada Irene, de la Fuente Villaverde Irene, Lozano-Blazquez Ana, Salgueiro Esther, Bordallo Javier, Santos-Juanes Jorge, Galache Osuna Cristina

机构信息

Unidad de Gestion Clínica de Dermatología, Hospital Universitario Central de Asturias, 33011 Oviedo, Spain.

Reumatology Department, Hospital Universitario de Santiago, 15706 Santiago de Compostela, Spain.

出版信息

Life (Basel). 2025 May 15;15(5):789. doi: 10.3390/life15050789.

DOI:10.3390/life15050789
PMID:40430215
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12113297/
Abstract

In routine clinical settings, identifying the factors that influence the persistence of biologic therapies is crucial for tailoring psoriasis management to individual patient profiles. This study aimed to evaluate the real-world drug survival of tildrakizumab in patients diagnosed with plaque psoriasis at the Dermatology Department of HUCA and to explore the clinical predictors of treatment discontinuation. We conducted a retrospective, hospital-based analysis involving 100 patients treated with tildrakizumab (Ilumetri) between 1 January 2021 and 30 April 2024. Kaplan-Meier estimates were used to construct survival curves, and multivariate analyses were performed using Cox proportional hazards regression models. Both crude and adjusted hazard ratios (HRs) were calculated to assess potential differences across patient subgroups. The multivariate analysis identified statistically significant associations between reduced drug survival and the presence of psoriatic arthritis ( = 0.02), previous biologic exposure ( = 0.02), and arterial hypertension ( = 0.012). Other comorbidities did not demonstrate significant effects. The most common reasons for treatment discontinuation were primary inefficacy and suboptimal response in patients with arthritis. Overall, tildrakizumab demonstrated robust survival outcomes in this patient population, though diminished persistence was observed in those with prior biologic use, comorbid arthritis, and hypertension.

摘要

在常规临床环境中,识别影响生物疗法持续使用的因素对于根据个体患者情况定制银屑病治疗方案至关重要。本研究旨在评估在HUCA皮肤科被诊断为斑块状银屑病的患者中替拉珠单抗的实际药物留存率,并探索治疗中断的临床预测因素。我们进行了一项基于医院的回顾性分析,纳入了2021年1月1日至2024年4月30日期间接受替拉珠单抗(Ilumetri)治疗的100例患者。采用Kaplan-Meier估计法构建生存曲线,并使用Cox比例风险回归模型进行多变量分析。计算了粗风险比和调整后风险比以评估不同患者亚组之间的潜在差异。多变量分析确定了药物留存率降低与银屑病关节炎的存在(P = 0.02)、既往生物制剂暴露(P = 0.02)和动脉高血压(P = 0.012)之间存在统计学显著关联。其他合并症未显示出显著影响。治疗中断的最常见原因是原发性无效和关节炎患者的反应欠佳。总体而言,替拉珠单抗在该患者群体中显示出良好的生存结果,尽管在既往使用过生物制剂、合并关节炎和高血压的患者中观察到留存率有所降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e95/12113297/e8612b3fe241/life-15-00789-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e95/12113297/e8612b3fe241/life-15-00789-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e95/12113297/e8612b3fe241/life-15-00789-g001.jpg

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本文引用的文献

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Dermatol Ther (Heidelb). 2025 Jun;15(6):1427-1440. doi: 10.1007/s13555-025-01416-z. Epub 2025 Apr 23.
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Long-term effectiveness and safety of risankizumab in patients with moderate-to-severe psoriasis with and without cardiometabolic comorbidities: a single-center retrospective study.伴有和不伴有心血管代谢合并症的中重度银屑病患者使用 risankizumab 的长期疗效和安全性:一项单中心回顾性研究。
J Dermatolog Treat. 2024 Dec;35(1):2425029. doi: 10.1080/09546634.2024.2425029. Epub 2024 Nov 7.
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Effectiveness of tildrakizumab 200 mg: an Italian multicenter study.特诺雅 200mg 的疗效:一项意大利多中心研究。
J Dermatolog Treat. 2024 Dec;35(1):2420825. doi: 10.1080/09546634.2024.2420825. Epub 2024 Oct 27.
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A 3-Year Experience with Tildrakizumab Treatment for Patients with Plaque Psoriasis in Clinical Practice.临床实践中使用替拉珠单抗治疗斑块状银屑病患者的3年经验
Dermatol Ther (Heidelb). 2024 Sep;14(9):2645-2652. doi: 10.1007/s13555-024-01252-7. Epub 2024 Aug 27.
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Tildrakizumab Real-World Effectiveness and Safety Over 64 Weeks in Patients With Moderate-to-Severe Plaque Psoriasis.替西罗莫司真实世界疗效和安全性:64 周中度至重度斑块状银屑病患者研究。
J Drugs Dermatol. 2024 Aug 1;23(8):612-618. doi: 10.36849/JDD.8217.
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Actas Dermosifiliogr. 2024 Jul-Aug;115(7):722-726. doi: 10.1016/j.ad.2023.08.019. Epub 2024 Mar 29.