guselkumab在银屑病关节炎中的实际疗效和保留:来自一项为期12个月的多中心研究的见解

IF 1.4 4区 医学 Q3 RHEUMATOLOGY
ARP Rheumatology Pub Date : 2025-07-01
Nicola Farina, Nicola Boffini, Antonella Adinolfi, Alberto Batticciotto, Alessandro Tomelleri, Adriana Cariddi, Stefania Calvisi, Elena Baldissera, Marco Matucci-Cerinic, Antonella Cappelli, Oscar Epis, Lorenzo Dagna
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引用次数: 0

摘要

背景:银屑病关节炎(PsA)是一种影响关节、皮肤和其他结构的慢性炎症性疾病。IL-23抑制剂Guselkumab在临床试验中显示出疗效,但其在PsA中长期使用的实际数据有限。本研究旨在评估guselkumab在真实PsA患者队列中超过12个月的有效性、安全性和保留率。方法:本回顾性研究包括三个医疗中心接受guselkumab治疗至少12个月的PsA患者。在基线和12个月时使用PsA疾病活动度评分对患者进行评估。记录12个月的保留率和停药原因。统计分析包括描述性统计、疾病活动性变化的曼-惠特尼检验和确定与停药相关因素的Cox回归。结果:我们纳入了70例PsA患者。在12个月时,DAS28、DAPSA、MASES和ASDAS的疾病活动性显著降低。12个月的保留率为79%,主要因无效而停药。无明显不良事件报道。Cox回归分析发现基线特征与停药之间无显著关联。结论:在真实PsA队列中,Guselkumab在降低疾病活动性和超过12个月的良好保留率方面表现出显著的疗效。这些发现支持guselkumab作为PsA的有效治疗方法,尽管需要进一步的前瞻性研究来证实其长期安全性和有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-world efficacy and retention of guselkumab in psoriatic arthritis: insights from a 12-month multicenter study.

Background: Psoriatic arthritis (PsA) is a chronic inflammatory disease that affects joints, skin, and other structures. Guselkumab, an IL-23 inhibitor, has shown efficacy in clinical trials, but real-world data on its long-term use in PsA are limited. This study aimed to assess the efficacy, safety, and retention rate of guselkumab in a real-world cohort of PsA patients over 12 months.

Methods: This retrospective study included PsA patients treated with guselkumab for at least 12 months across three medical centers. Patients were assessed at baseline and at 12 months using PsA disease activity scores. Retention rate at 12 months and reasons for discontinuation were recorded. Statistical analyses included descriptive statistics, Mann-Whitney tests for changes in disease activity, and Cox regression for identifying factors associated with treatment discontinuation.

Results: We included 70 PsA patients. Significant reductions in disease activity were observed at 12 months for DAS28, DAPSA, MASES and ASDAS. The 12-month retention rate was 79%, with discontinuation primarily due to inefficacy. No significant adverse events were reported. Cox regression analysis found no significant associations between baseline characteristics and treatment discontinuation.

Conclusions: Guselkumab demonstrated significant efficacy in reducing disease activity and a favorable retention rate over 12 months in a real-world PsA cohort. These findings support guselkumab as an effective treatment for PsA, although further prospective studies are needed to confirm long-term safety and efficacy.

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