根据疾病领域评估银屑病关节炎的真实世界证据:对CorEvitas银屑病关节炎/脊椎关节炎登记的评估。

Philip J Mease, Jacqueline O'Brien, Nicole Middaugh, Gregory Kricorian, Scott Stryker, David H Collier, Alexis Ogdie
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引用次数: 0

摘要

目的:实际研究评估银屑病关节炎(PsA)域的治疗反应是有限的。本研究旨在描述开始接受肿瘤坏死因子抑制剂(TNFi)或白细胞介素-17抑制剂(IL-17i)治疗的患者的PsA结构域的患者特征、频率和疾病结构域的组合、疾病活动性和患者报告的结果(PROs)。方法:纳入2013年1月至2021年1月期间开始接受TNFi或IL-17i治疗的成人PsA患者,并进行了6(±3)个月的随访。描述性地总结了PsA结构域的患病率、最常见的结构域组合、治疗持续性以及从基线到6个月每个PsA结构域的疾病活动性和PROs的未调整变化。结果:在1005例符合条件的患者中,63%接受TNFi治疗,37%接受IL-17i治疗。40%的TNFi和14%的IL-17i启动者接受了这些治疗作为一线治疗。外周关节炎和皮肤病是最常见的PsA结构域,分别在86%和82%的患者中发现,外周关节炎、皮肤病和指甲牛皮癣三合一是最常见的PsA结构域组合,在14%的患者中观察到。超过三分之二(68%)的患者在6个月的随访中仍在接受治疗。在接受TNFi或IL-17i治疗的患者中,所有PsA结构域的疾病活动性和PROs均有改善。结论:这一现实世界的分析突出了领域呈现的异质性;因此,评估所有PsA结构域对于优化疾病管理非常重要。所有PsA结构域的结果改善证明了TNFi和IL-17i在表现出不同PsA表型的不同患者组中的有效性。
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 Evidence Assessing Psoriatic Arthritis by Disease Domain: An Evaluation of the CorEvitas Psoriatic Arthritis/Spondyloarthritis Registry.

Real-World Evidence Assessing Psoriatic Arthritis by Disease Domain: An Evaluation of the CorEvitas Psoriatic Arthritis/Spondyloarthritis Registry.

Real-World Evidence Assessing Psoriatic Arthritis by Disease Domain: An Evaluation of the CorEvitas Psoriatic Arthritis/Spondyloarthritis Registry.

Real-World Evidence Assessing Psoriatic Arthritis by Disease Domain: An Evaluation of the CorEvitas Psoriatic Arthritis/Spondyloarthritis Registry.

Objective: Real-world studies assessing treatment response by psoriatic arthritis (PsA) domains are limited. This study aimed to describe the patient characteristics, frequency and combinations of disease domains, disease activity, and patient-reported outcomes (PROs) by PsA domains in patients who initiated treatment with a tumor necrosis factor inhibitor (TNFi) or interleukin-17 inhibitor (IL-17i).

Methods: Adults with PsA who initiated treatment with a TNFi or an IL-17i between January 2013 and January 2021 and had a 6 (±3)-month follow-up were included. The prevalence of PsA domains, the most common domain combinations, treatment persistence, and unadjusted change in disease activity and PROs from baseline to 6 months for each PsA domain were summarized descriptively.

Results: Of the 1005 eligible patients, 63% were receiving TNFi and 37% were receiving IL-17i. Forty percent of TNFi and 14% of IL-17i initiators received these treatments as first-line therapy. Peripheral arthritis and skin disease were the most common PsA domains identified in 86% and 82% of patients, respectively, and the triad of peripheral arthritis, skin disease, and nail psoriasis was the most common domain combination observed in 14% of patients. More than two thirds (68%) of patients remained on therapy at 6 months' follow-up. Improvements in disease activity and PROs were observed across all PsA domains in those receiving TNFi or IL-17i.

Conclusion: This real-world analysis highlights the heterogeneity in domain presentation; therefore, assessing all PsA domains is important for optimal disease management. Improvements in outcomes across all PsA domains demonstrate the effectiveness of TNFi and IL-17i in diverse patient groups exhibiting different phenotypes of PsA.

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