Department of Rheumatology, Zurich University Hospital, Zurich, Switzerland.
Statistics Group, Swiss Clinical Quality Management Foundation, Zurich, Switzerland.
Ann Rheum Dis. 2020 Sep;79(9):1203-1209. doi: 10.1136/annrheumdis-2019-215934. Epub 2020 Jun 24.
To compare effectiveness of treatment with secukinumab (SEC) with that of alternative tumour necrosis factor inhibitors (TNFis) in patients with axial spondyloarthritis (axSpA) after withdrawal from one or more TNFis.
Patients diagnosed as having axSpA in the Swiss Clinical Quality Management cohort were included if they had initiated SEC (n=106) or an alternative TNFi (n=284) after experiencing TNFi failure. Drug retention was investigated with matching weights propensity score (PS) analyses and multiple adjusted Cox proportional hazards models. Matching weights PS-based analyses and multiple-adjusted logistic regression analyses were used to assess the proportion of patients reaching 50% reduction in the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI50) at 1 year.
SEC was more often used as third-line or later-line biological drug (76% vs 40% for TNFi). Patients starting SEC had higher BASDAI, Bath Ankylosing Spondylitis Functional Index, Bath Ankylosing Spondylitis Metrology Index and C reactive protein levels. A comparable risk of drug discontinuation was found for SEC versus TNFi (HR 1.14, 95% CI 0.78 to 1.68 in the PS-based analysis and HR 1.16, 95% CI 0.79 to 1.71 in the multiple-adjusted analysis). No significant difference in BASDAI50 responses at 1 year was demonstrated between the two modes of biological drug action, with CI of estimates being, however, wide (OR for SEC vs TNFi 0.76, 95% CI 0.26 to 2.18 and 0.78, 95% CI 0.24 to 2.48 in the PS-based and the covariate-adjusted model, respectively).
Our data suggest a comparable effectiveness of SEC versus an alternative TNFi after prior TNFi exposure.
比较依奇珠单抗(SEC)与其他肿瘤坏死因子抑制剂(TNFi)在经历一种或多种 TNFi 治疗失败后用于治疗轴性脊柱关节炎(axSpA)患者的疗效。
在瑞士临床质量管理队列中诊断为 axSpA 的患者,如果在经历 TNFi 失败后开始使用 SEC(n=106)或另一种 TNFi(n=284),则将其纳入研究。采用匹配权重倾向评分(PS)分析和多调整 Cox 比例风险模型研究药物保留情况。采用匹配权重 PS 分析和多调整 logistic 回归分析评估在第 1 年达到巴斯强直性脊柱炎疾病活动指数(BASDAI50)降低 50%的患者比例。
SEC 更常作为三线或更后线生物药物使用(76% vs TNFi 的 40%)。开始使用 SEC 的患者 BASDAI、巴斯强直性脊柱炎功能指数、巴斯强直性脊柱炎衡量指数和 C 反应蛋白水平更高。SEC 与 TNFi 停药风险相当(PS 分析中 HR 为 1.14,95%CI 为 0.78 至 1.68;多调整分析中 HR 为 1.16,95%CI 为 0.79 至 1.71)。两种生物药物作用模式在第 1 年时 BASDAI50 反应无显著差异,但估计值置信区间较宽(SEC 与 TNFi 的比值比分别为 0.76,95%CI 为 0.26 至 2.18 和 0.78,95%CI 为 0.24 至 2.48,PS 分析和协变量调整模型)。
我们的数据表明,在先前接受 TNFi 治疗后,SEC 与其他 TNFi 的疗效相当。