Department of Rheumatology and Clinical Immunology, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Amsterdam Rheumatology and Immunology Center, Amsterdam, The Netherlands.
RMD Open. 2024 Oct 18;10(4):e004622. doi: 10.1136/rmdopen-2024-004622.
Early treatment of individuals at risk of developing rheumatoid arthritis (RA-risk) in the preclinical phase has the potential to positively impact both patients and society by preventing disease onset and improving patients' quality of life. The PRAIRI study was a randomised, double-blind, placebo-controlled trial with the B-cell depleting agent rituximab (RTX), which resulted in a significant delay of arthritis development of up to 12 months in seropositive RA-risk individuals. Here, we report our findings on patient-reported outcomes (PROs) in this study population.
Seventy-eight RA-risk individuals were treated with one single dose of either placebo (PBO) or 1000 mg RTX plus 100 mg methylprednisolone (MP) and anti-histamines, regardless of treatment allocation, as co-medication. Data on quality of life were collected at baseline and 1, 4, 6, 12 and 24 months using established PRO questionnaires (visual analogue scale (VAS) pain, health assessment questionnaire disability index (HAQ-DI) score, EuroQol five dimension (EQ-5D) and both physical and mental component score of the 36-item short-form heath survey (SF-36)).
No significant changes in quality of life over a 2 year follow-up were observed in at-risk individuals treated with RTX compared to PBO given the PRO scores at 24 months (mean difference±SEM: HAQ score=0.07±0.16; EQ-5D=-0.02±0.05; VAS pain=11.11±7.40). Furthermore, no significant effect of treatment on perceived arthritis severity at the time of clinically manifest disease (arthritis) was found.
One single dose of RTX plus MP administered to RA-risk individuals does not have a meaningful and measurable positive effect on PROs after 2 years of follow-up and/or perceived disease severity at the time of arthritis development.
Trial registered at EU Clinical Trial Register, EudraCT Number: 2009-010955-29 (https://www.clinicaltrialsregister.eu/ctr-search/search?query=Prevention+of+RA+by+B+cell+directed+therapy).
在临床前阶段对类风湿关节炎(RA)风险个体进行早期治疗,通过预防疾病发作和提高患者生活质量,有可能对患者和社会产生积极影响。PRAIRI 研究是一项随机、双盲、安慰剂对照试验,使用 B 细胞耗竭剂利妥昔单抗(RTX)治疗,结果显示,血清阳性 RA 风险个体的关节炎发病时间延迟长达 12 个月。在此,我们报告了该研究人群中患者报告结局(PRO)的研究结果。
78 名 RA 风险个体接受了单次安慰剂(PBO)或 1000mg RTX 加 100mg 甲基强的松龙(MP)和抗组胺药物治疗,无论治疗分配如何,均作为合并用药。使用既定的 PRO 问卷(视觉模拟量表(VAS)疼痛、健康评估问卷残疾指数(HAQ-DI)评分、欧洲五维健康量表(EQ-5D)和 36 项简明健康调查量表(SF-36)的身体和心理成分评分)在基线和 1、4、6、12 和 24 个月收集生活质量数据。
在 24 个月的 PRO 评分中,与 PBO 相比,接受 RTX 治疗的高危个体在 2 年随访期间生活质量无显著变化(平均差异±SEM:HAQ 评分=0.07±0.16;EQ-5D=-0.02±0.05;VAS 疼痛=11.11±7.40)。此外,在临床显性疾病(关节炎)时,治疗对感知关节炎严重程度也没有显著影响。
高危个体单次接受 RTX 加 MP 治疗,在 2 年随访期间,对 PRO 无明显和可衡量的积极影响,也无法改善关节炎发病时的感知疾病严重程度。
在欧盟临床试验注册中心注册,EudraCT 编号:2009-010955-29(https://www.clinicaltrialsregister.eu/ctr-search/search?query=Prevention+of+RA+by+B+cell+directed+therapy)。