幼年特发性关节炎生物药物的选择和转换。

Seher Şener, Özge Başaran, Ezgi Deniz Batu, Müşerref Kasap Cüceoğlu, Zeynep Balık, Emil Aliyev, Yağmur Bayındır, Yelda Bilginer, Seza Özen
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引用次数: 0

摘要

背景本研究旨在根据疾病亚型评估幼年特发性关节炎(JIA)患者对生物制剂药物的选择和变化:我们对2004年1月至2022年7月期间接受生物制剂治疗的JIA患者进行了回顾性分析:在294例JIA患者中,80例(27.2%)为全身性JIA,68例(23.1%)为少关节型JIA,61例(20.7%)为多关节型JIA,79例(26.9%)为关节炎相关性关节炎(ERA),6例(2.1%)为银屑病关节炎(PsA)。Anakinra(66人,82.5%)是全身性JIA最常用的一线生物制剂。Etanercept是ERA(69人,87.3%)、少关节型(37人,54.4%)和多关节型JIA(43人,70.5%)患者最常使用的生物制剂药物。阿达木单抗是所有PsA患者(6人,100%)的一线生物药物。有14名患者(38.8%)转用二线生物制剂药物,29名患者(9.9%)转用三线生物制剂药物。全身性JIA患者转用二线生物制剂的最常见原因是难以使用每日注射(37人,60.6%),而非全身性JIA患者转用二线生物制剂的最常见原因是对一线生物制剂的反应不足(42人,79.2%)。在随访期间,仅有7名患者(2.4%)出现副作用:在这项研究中,我们揭示了JIA患者的生物制剂使用和转换策略。大多数患者的反应良好,情况可靠。然而,要澄清这些结果,还需要对更大的患者群体进行研究。
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Choice and switch of biologic drugs in juvenile idiopathic arthritis.

Background: In this study, we aimed to evaluate choices and changes of biologic drugs in juvenile idiopathic arthritis (JIA) patients according to disease subtypes.

Methods: We retrospectively analyzed JIA patients who received biologic treatment between January 2004 and July 2022.

Results: Of 294 JIA patients, 80 (27.2%) had systemic JIA, 68 (23.1%) had oligoarticular JIA, 61 (20.7%) had polyarticular JIA, 79 (26.9%) had enthesitis-associated arthritis (ERA), and six (2.1%) had psoriatic arthritis (PsA). Anakinra (n=66, 82.5%) was the most commonly preferred first line biologic in systemic JIA. Etanercept was the most frequently used biologic drug in patients with ERA (n=69, 87.3%), oligoarticular (n=37, 54.4%) and polyarticular JIA (n=43, 70.5%). Adalimumab was used as a first-line biologic drug in all PsA patients (n=6, 100%). One hundred-fourteen patients (38.8%) were switched to second-line and 29 (9.9%) to third-line biologic drugs. While the most common reason for switching to a second-line biologic was difficulty in usage of daily injections (n=37, 60.6%) in systemic JIA patients, it was an inadequate response to first biologics in non-systemic JIA patients (n=42, 79.2%). Side effects were detected in only seven patients (2.4%) during the follow-up.

Conclusion: In this study, we revealed the biologic drug usage and switch strategies in our JIA patients. Good responses were obtained in most of our patients with a reliable profile. However, studies on larger patient groups are needed to clarify these results.

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