Reina Sofia University Hospital, Instituto Maimónides de Investigación Biomédica de Córdoba, University of Cordoba, Cordoba, Spain, and Université Paris Cité, Centre de Recherche Épidémiologie et Bio Statistique de Sorbonne Paris Cité, Assistance Publique-Hôpitaux de Paris, Hôpital Cochin, Paris, France.
VIB Center for Inflammation Research, Ghent University, Belgium.
Arthritis Care Res (Hoboken). 2024 Nov;76(11):1540-1548. doi: 10.1002/acr.25387. Epub 2024 Jul 14.
The objective of this study was to evaluate the impact of protocol violations in the treat-to-target group in the Tight Control in Spondyloarthritis (TICOSPA) trial and to compare the proportion of patients optimally treated according to the Assessment of Spondyloarthritis International Society (ASAS)/EULAR 2016 recommendations for patients with axial spondyloarthritis (axSpA) between the treat-to-target versus usual care (UC) arms.
This study was a cluster-randomized, controlled 48-week trial including patients with axSpA who fulfilled the ASAS criteria, had an Axial Spondyloarthritis Disease Activity Score >2.1, and were biologic disease-modifying antirheumatic drug naive. Eighteen axSpA expert centers were randomly allocated to one treatment arm: (a) treat-to-target prespecified management strategy (four-week visits), and (b) UC treatment decisions at the rheumatologist's discretion (12-week visits). Protocol violations in the treat-to-target arm and the fulfillment of the 2016 ASAS/EULAR recommendations in both arms were evaluated at every visit. ASAS Health Index (ASAS-HI) and disease activity outcomes at 48 weeks were compared between treat-to-target violators versus nonviolators. Patients treated according to the ASAS/EULAR recommendations were compared between both arms.
A total of 160 patients initiated the trial (80 patients with treat to target; 80 patients with UC). In the treat-to-target arm, 51.2% patients violated the protocol at least once (62.2% of violations resulting in maintenance/reduction of treatment against protocol). After 48 weeks, treat-to-target violators versus nonviolators showed similar ratios of ASAS-HI improvement. The proportion of patients managed according to the ASAS/EULAR recommendations after the first 12 weeks were 63.9% versus 61.8% for the treat-to-target and UC arms, respectively.
Protocol violations in the treat-to-target arm in the TICOSPA trial were frequent, although they did not have an impact on the rate of the primary outcome. The groups with UC was optimally treated, partly explaining the nonachievement of the primary objective in the TICOSPA trial.
本研究旨在评估 Tight Control in Spondyloarthritis(TICOSPA)试验中靶向治疗组的方案违反情况,并比较符合强直性脊柱炎国际评估协会(ASAS)/欧洲抗风湿病联盟(EULAR)2016 年推荐的轴性脊柱关节炎(axSpA)患者按照治疗目标与常规治疗(UC)的比例。
这是一项集群随机对照的 48 周试验,纳入了符合 ASAS 标准、Axial Spondyloarthritis Disease Activity Score(ASDAS)>2.1 和生物疾病修饰抗风湿药物初治的 axSpA 患者。18 个 axSpA 专家中心被随机分配到一个治疗组:(a)治疗目标预设管理策略(四周就诊),和(b)风湿病医生自行决定的 UC 治疗决策(12 周就诊)。在每次就诊时评估靶向治疗组的方案违反情况和两臂均符合 2016 年 ASAS/EULAR 建议的情况。比较 48 周时的 ASAS 健康指数(ASAS-HI)和疾病活动结果。比较治疗目标违反者与非违反者之间的治疗情况。
共有 160 名患者开始参与试验(80 名患者采用治疗目标,80 名患者采用 UC)。在靶向治疗组中,51.2%的患者至少违反了一次方案(62.2%的违反导致治疗方案维持/减少)。48 周后,治疗目标违反者与非违反者的 ASAS-HI 改善比例相似。在最初的 12 周后,根据 ASAS/EULAR 建议进行管理的患者比例分别为治疗目标组的 63.9%和 UC 组的 61.8%。
TICOSPA 试验中靶向治疗组的方案违反情况频繁,但并未对主要结局的发生率产生影响。UC 组得到了最佳治疗,部分解释了 TICOSPA 试验未达到主要目标的原因。