Department of Rheumatology, Zurich University Hospital, University of Zurich, Zurich, Switzerland
Swiss Clinical Quality Management Foundation, Zurich, Switzerland.
RMD Open. 2023 Dec 1;9(4):e003455. doi: 10.1136/rmdopen-2023-003455.
To characterise the population fulfilling the Assessment of SpondyloArthritis international Society (ASAS) consensus definition of early axial spondyloarthritis (axSpA) and to determine the effectiveness of a first tumour necrosis factor inhibitor (TNFi) in early versus established axSpA in a large observational registry.
A total of 3064 patients with axSpA in the Swiss Clinical Quality Management registry with data on duration of axial symptoms were included (≤2 years=early axSpA, N=658; >2 years=established axSpA, N=2406). Drug retention was analysed in patients starting a first TNFi in early axSpA (N=250) versus established axSpA (N=874) with multiple-adjusted Cox proportional hazards models. Adjusted logistic regression analyses were used to determine the achievement of the ASAS criteria for 40% improvement (ASAS40) at 1 year.
Sex distribution, disease activity, impairments of function and health-related quality of life were comparable between patients with early and established axSpA. Patients with established disease were older, had more prevalent axial radiographical damage and had a higher impairment of mobility. A comparable TNFi retention was found in early versus established disease after adjustment for age, sex, human leucocyte antigen-B27 status, education, body mass index, smoking, elevated C reactive protein and sacroiliac inflammation on MRI (HR 1.05, 95% CI 0.78 to 1.42). The adjusted ASAS40 response was similar in the two groups (OR 1.09, 95% CI 0.67 to 1.78). Results were confirmed in the population fulfilling the ASAS classification criteria.
Considering the recent ASAS definition of early axSpA, TNFi effectiveness seems comparable in early versus established disease.
描述符合脊柱关节炎国际学会(ASAS)早期中轴型脊柱关节炎(axSpA)共识定义的人群特征,并在大型观察性登记处确定早期与已确立的 axSpA 中首次使用肿瘤坏死因子抑制剂(TNFi)的疗效。
瑞士临床质量管理登记处共纳入 3064 例 axSpA 患者,这些患者有关于轴症状持续时间的数据(≤2 年=早期 axSpA,N=658;>2 年=已确立的 axSpA,N=2406)。在早期 axSpA(N=250)和已确立的 axSpA(N=874)中,对开始使用首次 TNFi 的患者进行药物保留分析,采用多调整 Cox 比例风险模型。采用调整后的逻辑回归分析确定在 1 年时达到 40%改善的 ASAS 标准(ASAS40)的情况。
早期和已确立的 axSpA 患者的性别分布、疾病活动度、功能损害和健康相关生活质量相当。患病时间较长的患者年龄较大,更常见有轴向影像学损害,且活动能力受损更严重。在调整年龄、性别、人类白细胞抗原-B27 状态、教育程度、体重指数、吸烟、C 反应蛋白升高和 MRI 上的骶髂关节炎症后,早期和已确立的疾病之间发现了类似的 TNFi 保留率(HR 1.05,95%CI 0.78 至 1.42)。两组的调整后 ASAS40 反应相似(OR 1.09,95%CI 0.67 至 1.78)。在符合 ASAS 分类标准的人群中,结果得到了证实。
考虑到最近的 ASAS 早期 axSpA 定义,早期与已确立的疾病中 TNFi 的疗效似乎相当。