Università di Genova, Genoa, Italy.
Arthritis Care Res (Hoboken). 2010 Nov;62(11):1542-51. doi: 10.1002/acr.20283. Epub 2010 Jul 1.
To assess health-related quality of life (HRQOL) in abatacept-treated children/adolescents with juvenile idiopathic arthritis (JIA).
In this phase III, double-blind, placebo-controlled trial, subjects with active polyarticular course JIA and an inadequate response/intolerance to ≥1 disease-modifying antirheumatic drug (including biologics) received abatacept 10 mg/kg plus methotrexate (MTX) during the 4-month open-label period (period A). Subjects achieving the American College of Rheumatology Pediatric 30 criteria for improvement (defined "responders") were randomized to abatacept or placebo (plus MTX) in the 6-month double-blind withdrawal period (period B). HRQOL assessments included 15 Child Health Questionnaire (CHQ) health concepts plus the physical (PhS) and psychosocial summary scores (PsS), pain (100-mm visual analog scale), the Children's Sleep Habits Questionnaire, and a daily activity participation questionnaire.
A total of 190 subjects from period A and 122 from period B were eligible for analysis. In period A, there were substantial improvements across all of the CHQ domains (greatest improvement was in pain/discomfort) and the PhS (8.3 units) and PsS (4.3 units) with abatacept. At the end of period B, abatacept-treated subjects had greater improvements versus placebo in all domains (except behavior) and both summary scores. Similar improvement patterns were seen with pain and sleep. For participation in daily activities, an additional 2.6 school days/month and 2.3 parents' usual activity days/month were gained in period A responders with abatacept, and further gains were made in period B (1.9 versus 0.9 [P = 0.033] and 0.2 versus -1.3 [P = 0.109] school days/month and parents' usual activity days/month, respectively, in abatacept- versus placebo-treated subjects).
Improvements in HRQOL were observed with abatacept, providing real-life tangible benefits to children with JIA and their parents/caregivers.
评估阿巴西普治疗幼年特发性关节炎(JIA)儿童/青少年的健康相关生活质量(HRQOL)。
在这项 III 期、双盲、安慰剂对照试验中,患有活动性多关节病程 JIA 且对≥1 种疾病修饰抗风湿药物(包括生物制剂)治疗反应不足/不耐受的患者在 4 个月的开放标签期(A 期)接受阿巴西普 10mg/kg 加甲氨蝶呤(MTX)治疗。达到美国风湿病学会儿科 30 项改善标准(定义为“应答者”)的患者在 6 个月的双盲停药期(B 期)被随机分配至阿巴西普或安慰剂(加 MTX)组。HRQOL 评估包括 15 项儿童健康问卷(CHQ)健康概念,以及身体(PhS)和心理社会总评分(PsS)、疼痛(100mm 视觉模拟量表)、儿童睡眠习惯问卷和日常活动参与问卷。
A 期的 190 名患者和 B 期的 122 名患者符合分析条件。在 A 期,阿巴西普治疗后所有 CHQ 领域(疼痛/不适改善最大)和 PhS(8.3 个单位)和 PsS(4.3 个单位)均有显著改善。在 B 期结束时,与安慰剂相比,阿巴西普治疗的患者在所有领域(行为除外)和两个总评分均有更大的改善。疼痛和睡眠也呈现出相似的改善模式。对于日常活动的参与度,在 A 期应答者中,阿巴西普治疗的患者每月额外增加 2.6 个上学日/月和 2.3 个父母日常活动日/月,在 B 期进一步增加(阿巴西普治疗与安慰剂治疗相比,分别为 1.9 对 0.9[P=0.033]和 0.2 对-1.3[P=0.109]上学日/月和父母日常活动日/月)。
阿巴西普治疗可改善 HRQOL,为 JIA 患儿及其父母/照顾者带来实际的生活获益。