Giulia Frazzei, Sophie H M Cramer, Robert B M Landewé, Karen I Maijer, Danielle M Gerlag, Paul P Tak, Niek de Vries, Lisa G M van Baarsen, Ronald F van Vollenhoven, Sander W Tas
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Here, we report our findings on patient-reported outcomes (PROs) in this study population.</p><p><strong>Methods: </strong>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)).</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p><p><strong>Trial registration number: </strong>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).</p>","PeriodicalId":21396,"journal":{"name":"RMD Open","volume":null,"pages":null},"PeriodicalIF":5.1000,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11492957/pdf/","citationCount":"0","resultStr":"{\"title\":\"The effect of rituximab on patient reported outcomes in the preclinical phase of rheumatoid arthritis: 2 year data from the PRAIRI study.\",\"authors\":\"Giulia Frazzei, Sophie H M Cramer, Robert B M Landewé, Karen I Maijer, Danielle M Gerlag, Paul P Tak, Niek de Vries, Lisa G M van Baarsen, Ronald F van Vollenhoven, Sander W Tas\",\"doi\":\"10.1136/rmdopen-2024-004622\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>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. 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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)).</p><p><strong>Results: </strong>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). 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引用次数: 0
摘要
目标:在类风湿关节炎(RA-risk)临床前阶段对有发病风险的患者进行早期治疗,有可能通过预防发病和改善患者的生活质量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 细胞清除剂利妥昔单抗(RTX)后,血清反应阳性的类风湿性关节炎高危人群的关节炎发展显著延迟了 12 个月。在此,我们报告了在该研究人群中患者报告的结果(PROs):78名RA高危人群接受了单剂量安慰剂(PBO)或1000毫克RTX加100毫克甲基强的松龙(MP)和抗组胺药物的治疗,无论治疗分配如何,均为联合用药。在基线和1、4、6、12和24个月时,使用已建立的PRO问卷收集生活质量数据(疼痛视觉模拟量表(VAS)、健康评估问卷残疾指数(HAQ-DI)得分、EuroQol五维(EQ-5D)以及36项短式健康调查(SF-36)的身体和精神部分得分):从24个月的PRO评分来看,与PBO相比,接受RTX治疗的高危人群在2年随访期间的生活质量没有发生明显变化(平均差±SEM:HAQ评分=0.07±0.16;EQ-5D=-0.02±0.05;VAS疼痛=11.11±7.40)。此外,治疗对临床表现疾病(关节炎)时感知的关节炎严重程度没有明显影响:结论:对有RA风险的个体施用单剂量RTX加MP治疗对随访2年后的PROs和/或关节炎发展时的感知疾病严重程度没有有意义且可测量的积极影响:试验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)。
The effect of rituximab on patient reported outcomes in the preclinical phase of rheumatoid arthritis: 2 year data from the PRAIRI study.
Objectives: 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.
Methods: 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)).
Results: 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.
Conclusion: 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 registration number: 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).
期刊介绍:
RMD Open publishes high quality peer-reviewed original research covering the full spectrum of musculoskeletal disorders, rheumatism and connective tissue diseases, including osteoporosis, spine and rehabilitation. Clinical and epidemiological research, basic and translational medicine, interesting clinical cases, and smaller studies that add to the literature are all considered.