Ishchenko Alla, Joly Johan, Neerinckx Barbara, Lories Rik, de Vlam Kurt
Department of Rheumatology, University Hospitals Leuven.
Skeletal Biology and Engineering Research Centre, Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
Rheumatol Adv Pract. 2021 Nov 15;5(3):rkab085. doi: 10.1093/rap/rkab085. eCollection 2021.
Biologic treatments have revolutionized the management of PsA by significantly improving clinical manifestations and preventing structural damage. Both result in better quality of life and improved physical functioning. Since the introduction of the first TNF inhibitor (TNFi) in the early 2000s, therapeutic options for PsA are increasing steadily, and a new generation of biologics, including anti-IL-17 and anti-IL-23 strategies, allows distinct targeted approaches. The purpose of this study was to investigate whether the demographic, clinical and disease characteristics of PsA patients who are selected for first-line biologic treatment has changed over time since the introduction of biologics.
Patients with a clinical diagnosis of PsA were included in the KU Leuven BioSPAR registry, a prospective cohort of SpA and PsA patients treated with biologics and targeted synthetic DMARDs (tsDMARDs), such as apremilast and Janus kinase inhibitors. Demographics, prior DMARD use, disease characteristics and disease activity parameters were recorded at the initiation of biologic treatment and subsequently every 3 months for the first 2 years and later every 6 months. The patient data were compared in three treatment periods, corresponding to availability of the first and second generation of TNFi and the third generation of biologics.
Analysis of 185 Caucasian patients with PsA from our prospective cohort showed longer disease duration and higher disease activity, with higher tender joint count, swollen joint count and CRP in the first period compared with the later time periods. The demographic characteristics and prior DMARD use did not change over time. Skin and nail psoriasis were more frequent in earlier compared with the later treatment periods. The bio-DMARD survival rate was similar in the early and later treatment periods.
The population of patients selected for treatment escalation has changed over time since the introduction of biologics. Our results suggest that with years of experience, PsA patients might be considered earlier and for therapy intensification in patients with less active disease in comparison to profiles in the early days of biologic treatment.
生物治疗通过显著改善临床表现和预防结构损伤,彻底改变了银屑病关节炎(PsA)的治疗方式。这两者都能带来更好的生活质量和身体功能改善。自21世纪初首款肿瘤坏死因子抑制剂(TNFi)问世以来,PsA的治疗选择稳步增加,包括抗白细胞介素-17和抗白细胞介素-23策略在内的新一代生物制剂提供了不同的靶向治疗方法。本研究的目的是调查自生物制剂引入以来,被选用于一线生物治疗的PsA患者的人口统计学、临床和疾病特征是否随时间发生了变化。
临床诊断为PsA的患者被纳入鲁汶大学(KU Leuven)生物SPAR注册研究,这是一个前瞻性队列,纳入接受生物制剂和靶向合成改善病情抗风湿药(tsDMARDs)(如阿普司特和Janus激酶抑制剂)治疗的脊柱关节炎(SpA)和PsA患者。在开始生物治疗时记录人口统计学、既往DMARD使用情况、疾病特征和疾病活动参数,随后在头2年每3个月记录一次,之后每6个月记录一次。将患者数据在三个治疗时期进行比较,分别对应第一代和第二代TNFi以及第三代生物制剂的可获得情况。
对我们前瞻性队列中的185例白种人PsA患者进行分析显示,与后期相比,第一个时期的疾病持续时间更长、疾病活动度更高,压痛关节数、肿胀关节数和C反应蛋白(CRP)更高。人口统计学特征和既往DMARD使用情况未随时间变化。与后期治疗时期相比,早期皮肤和指甲银屑病更为常见。早期和后期治疗时期的生物改善病情抗风湿药生存率相似。
自生物制剂引入以来,被选用于治疗升级的患者群体随时间发生了变化。我们的结果表明,与生物治疗早期的情况相比,随着多年经验的积累,对于疾病活动度较低的患者,可能会更早考虑并加强对PsA患者的治疗。