Hopital Cochin, Rheumatology, Université Paris Descartes Faculté de Médecine, Paris, France
Biostatistics RCTs Clinical Research Organization, Lyon, France.
RMD Open. 2024 Feb 29;10(1):e003942. doi: 10.1136/rmdopen-2023-003942.
To compare the 1-year retention rate of secukinumab in axial spondyloarthritis (axSpA) and its predisposing factors with regard to its time of initiation (eg, right after or remotely from its launch).
Study design: Retrospective multicentre French study of patients with axSpA. Study periods: Two cohorts were evaluated regarding the time of initiation of secukinumab: cohort 1 (C1)-between 16 August 2016 and 31 August 2018-and cohort 2 (C2)-between 1 September 2018 and 13 November 2020.
The 1-year retention rate of secukinumab was estimated using the Kaplan-Meier method, and the log-rank test was used to compare the retention curves of the two cohorts. Preselected factors (eg, disease characterristics, line and time of secukinumab initiation) of secukinumab retention at 1 year were analysed by univariate and multivariate Cox model regression.
In total, 906 patients in C1 and 758 in C2 from 50 centres were included in the analysis. The 1-year retention rate was better in C2 (64% (61%-68%)) vs C1 (59% (55%-62%)) (HR=1.19 (1.02-1.39); p=0.0297). In the multivariate analysis, the line of biologic therapy was the single predictive factor of the 1-year retention rate of secukinumab picked up in both cohorts, with a better retention rate when prescribed as first-line biologic therapy.
The better secukinumab retention rate remotely from its launch is explained by its use at an earlier stage of the disease, suggesting a change in the behaviour of prescribing physicians. Our results emphasise the relevance of iterative evaluations of routine care treatments.
比较司库奇尤单抗治疗中轴型脊柱关节炎(axSpA)的 1 年保留率及其启动时间的相关影响因素(例如,刚上市时或上市后很久)。
研究设计:回顾性多中心法国 axSpA 患者研究。研究时段:根据司库奇尤单抗的启动时间评估了两个队列:队列 1(C1)-2016 年 8 月 16 日至 2018 年 8 月 31 日-和队列 2(C2)-2018 年 9 月 1 日至 2020 年 11 月 13 日。
采用 Kaplan-Meier 法估计司库奇尤单抗的 1 年保留率,并采用对数秩检验比较两个队列的保留曲线。通过单因素和多因素 Cox 模型回归分析司库奇尤单抗 1 年保留率的预先选定因素(例如,疾病特征、司库奇尤单抗的起始时间和药物种类)。
共纳入 50 个中心的 C1 组 906 例和 C2 组 758 例患者。C2 组(64%(61%-68%))的 1 年保留率优于 C1 组(59%(55%-62%))(HR=1.19(1.02-1.39);p=0.0297)。多因素分析中,生物治疗线是两个队列中司库奇尤单抗 1 年保留率的唯一预测因素,作为一线生物治疗药物时保留率更高。
司库奇尤单抗上市后很久的保留率更好,这与疾病早期使用该药有关,提示处方医生的行为发生了变化。我们的研究结果强调了对常规治疗进行迭代评估的重要性。