Division of Immunology/Rheumatology, Stanford University School of Medicine, 306 Ramona Road, Portola Valley, CA 94028, USA.
J Rheumatol. 2012 Jan;39(1):63-72. doi: 10.3899/jrheum.101161. Epub 2011 Nov 1.
Rheumatoid arthritis (RA) is associated with significant impairments in health-related quality of life (HRQOL). We evaluated patient-reported outcomes including HRQOL outcomes following adalimumab plus methotrexate (MTX) therapy in patients with early RA.
PREMIER was a phase III, multicenter, randomized, double-blind, active-comparator clinical trial in early RA. Patients aged ≥ 18 years were randomly assigned to receive adalimumab 40 mg every other week (eow) plus weekly MTX, weekly MTX, or adalimumab 40 mg eow for 104 weeks. American College of Rheumatology (ACR) criteria were used to evaluate clinical efficacy and response. Outcomes were assessed using the Health Assessment Questionnaire Disability Index (HAQ-DI), Short-Form 36 Health Survey (SF-36), Short-Form 6 Dimension (SF-6D), visual analog scale (VAS) assessments of global disease activity (patient's global assessment; PtGA) and pain, Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F), and Health Utility Index Mark 3 (HUI-3).
Of 799 patients enrolled, 268 received adalimumab plus MTX, 257 received MTX monotherapy, and 274 received adalimumab monotherapy. Patients treated with adalimumab plus MTX demonstrated significant baseline to Week 104 improvements in HAQ-DI (p < 0.0001), SF-36 Physical Component Summary (p < 0.0001), 4 SF-36 domains [physical function (p < 0.0001), bodily pain (p <0.0001), vitality (p = 0.0139), role limitations-physical (p = 0.0005)], SF-6D (p = 0.0152), VAS-PtGA (p < 0.0001), VAS-pain (p < 0.0001), FACIT-F (p < 0.0001), and HUI-3 (p = 0.0034) scores versus patients treated with MTX monotherapy. Both SF-6D and HUI-3 were found to be sensitive preference-based measures for assessing the effects of treatment on multidimensional function. No clinically meaningful differences between adalimumab and MTX monotherapy groups were observed for most measures. For each measure, there was significant association between HRQOL improvement and ACR clinical response.
Adalimumab plus MTX significantly improved physical functioning and HRQOL in patients with early RA over 2 years of treatment. (ClinicalTrials.gov identifier NCT00195663).
类风湿关节炎(RA)与健康相关生活质量(HRQOL)显著受损有关。我们评估了阿达木单抗联合甲氨蝶呤(MTX)治疗早期 RA 患者后的患者报告结局,包括 HRQOL 结局。
PREMIER 是一项针对早期 RA 的 III 期、多中心、随机、双盲、活性对照临床试验。年龄≥18 岁的患者被随机分配接受阿达木单抗 40mg 每两周一次(eow)加每周 MTX、每周 MTX 或阿达木单抗 40mg eow 治疗 104 周。美国风湿病学会(ACR)标准用于评估临床疗效和反应。使用健康评估问卷残疾指数(HAQ-DI)、36 项简短健康调查(SF-36)、6 维度简短量表(SF-6D)、全球疾病活动的视觉模拟量表评估(患者总体评估;PtGA)和疼痛、慢性病治疗疲劳的功能评估-疲劳量表(FACIT-F)以及健康效用指数标记 3(HUI-3)评估结局。
在 799 名入组患者中,268 名接受阿达木单抗联合 MTX 治疗,257 名接受 MTX 单药治疗,274 名接受阿达木单抗单药治疗。接受阿达木单抗联合 MTX 治疗的患者在基线至第 104 周时,HAQ-DI(p<0.0001)、SF-36 生理成分综合评分(p<0.0001)、4 个 SF-36 领域[生理功能(p<0.0001)、躯体疼痛(p<0.0001)、活力(p=0.0139)、身体受限-生理(p=0.0005)]、SF-6D(p=0.0152)、PtGA 视觉模拟量表(p<0.0001)、疼痛视觉模拟量表(p<0.0001)、FACIT-F(p<0.0001)和 HUI-3(p=0.0034)评分均显著改善,而接受 MTX 单药治疗的患者则无显著改善。SF-6D 和 HUI-3 均被发现是评估治疗对多维功能影响的敏感偏好测量指标。在大多数测量指标中,阿达木单抗和 MTX 单药治疗组之间没有观察到有临床意义的差异。对于每个测量指标,HRQOL 改善与 ACR 临床反应之间均有显著关联。
阿达木单抗联合 MTX 可显著改善早期 RA 患者的身体功能和 HRQOL,治疗时间超过 2 年。(临床试验注册号 NCT00195663)。