Continuous improvement through differential trajectories of individual minimal disease activity criteria with guselkumab in active psoriatic arthritis: post hoc analysis of a phase 3, randomized, double-blind, placebo-controlled study

IF 2.1 Q3 RHEUMATOLOGY
Laura C. Coates, Proton Rahman, Philip J. Mease, May Shawi, Emmanouil Rampakakis, Alexa P. Kollmeier, Xie L. Xu, Soumya D. Chakravarty, Iain B. McInnes, Lai-Shan Tam
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Abstract

To explore the trajectory of, and factors contributing to, achievement of individual criteria of minimal disease activity (MDA) in patients with active psoriatic arthritis (PsA) treated with guselkumab. The Phase 3, randomized, placebo-controlled DISCOVER-2 study enrolled adults (N = 739) with active PsA despite standard therapies who were biologic/Janus kinase inhibitor-naive. Patients were randomized 1:1:1 to guselkumab 100 mg every 4 weeks; guselkumab 100 mg at week 0, week 4, then every 8 weeks; or placebo. In this post hoc analysis, patients randomized to guselkumab were included and pooled (N = 493). Longitudinal trajectories of achieving each MDA criterion through week 100 were derived using non-responder imputation. Time to achieve each criterion was estimated with Kaplan-Meier analysis. Multivariate regression for time to achieve each criterion (Cox regression) and achievement at week 100 (logistic regression) was used to identify contributing factors. Continuous improvement across all MDA domains was shown over time. ~70% of patients achieved near remission in swollen joint count (SJC), Psoriasis Area and Severity Index (PASI), and enthesitis through week 100. Median times to achieve individual criteria differed significantly (p < 0.0001), with SJC ≤ 1 (20 weeks), PASI ≤ 1 (16 weeks), and ≤ 1 tender entheses (16 weeks) being faster than patient-reported criteria (pain ≤ 15 mm, patient global assessment of arthritis and psoriasis ≤ 20 mm, Health Assessment Questionnaire-Disability Index ≤ 0.5) and tender joint count ≤ 1. Higher baseline domain scores, older age, worse fatigue, and increased body mass index were significant predictors of longer time to achieve minimal levels of disease activity assessed via patient-reported criteria. Substantial proportions of guselkumab-treated patients achieved individual MDA criteria, each showing continuous improvement through week 100, although with distinct trajectories. Median times to achieve physician-assessed MDA criteria were significantly faster compared with patient-driven criteria. Identification of modifiable factors affecting the time to achieve patient-reported criteria has the potential to optimize the achievement and sustainability of MDA in the clinic via a multidisciplinary approach to managing PsA, involving both medical and lifestyle interventions. NCT03158285. May 16, 2017.
活动性银屑病关节炎患者使用古舍库单抗后,通过个体最小疾病活动度标准的不同轨迹实现持续改善:对一项 3 期随机、双盲、安慰剂对照研究的事后分析
探索接受古舍库单抗治疗的活动性银屑病关节炎(PsA)患者达到最小疾病活动度(MDA)个体标准的轨迹及促成因素。3期随机安慰剂对照DISCOVER-2研究招募了接受标准疗法后仍有活动性银屑病关节炎且未使用生物制剂/Janus激酶抑制剂的成人患者(N = 739)。患者按1:1:1的比例随机分配到每4周100毫克的古谢库单抗;第0周、第4周、然后每8周100毫克的古谢库单抗;或安慰剂。在这项事后分析中,纳入并汇总了随机接受古舍库单抗治疗的患者(N = 493)。使用非应答者归因法得出了到第 100 周达到每项 MDA 标准的纵向轨迹。通过 Kaplan-Meier 分析估算了达到各项标准的时间。对达到每项标准的时间(Cox 回归)和第 100 周达到标准的时间(Logistic 回归)进行多元回归,以确定诱因。随着时间的推移,所有 MDA 领域均出现持续改善。~到第 100 周时,约 70% 的患者在关节肿胀计数 (SJC)、银屑病面积和严重程度指数 (PASI) 以及关节炎方面达到接近缓解。达到各项标准的中位时间差异显著(p < 0.0001),SJC ≤ 1(20 周)、PASI ≤ 1(16 周)和触痛性关节炎≤ 1(16 周)快于患者报告的标准(疼痛≤ 15 毫米、患者对关节炎和银屑病的全面评估≤ 20 毫米、健康评估问卷-残疾指数≤ 0.5)和触痛性关节炎≤ 1。基线领域得分越高、年龄越大、疲劳程度越严重以及体重指数越高,都是通过患者报告标准评估疾病活动达到最低水平所需时间越长的重要预测因素。接受古舍库单抗治疗的患者中有相当一部分达到了单项MDA标准,每项标准在第100周前都有持续改善,但轨迹各不相同。与患者主导的标准相比,达到医生评估的MDA标准的中位时间明显更快。找出影响达到患者报告标准时间的可调节因素,有可能通过多学科方法(包括医疗和生活方式干预)来管理PsA,从而优化MDA在临床中的实现和可持续性。NCT03158285。2017年5月16日
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来源期刊
BMC Rheumatology
BMC Rheumatology Medicine-Rheumatology
CiteScore
3.80
自引率
0.00%
发文量
73
审稿时长
15 weeks
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