Division of Rheumatology, Allergy, and Immunology, San Diego, CA, USA.
Curr Med Res Opin. 2010 Oct;26(10):2385-92. doi: 10.1185/03007995.2010.515804.
To use data from a phase II clinical trial to evaluate the effect of ustekinumab, a human immunoglobulin monoclonal antibody that binds with high affinity to the shared p40 subunit of human interleukins-12 and -23, on physical disability and health-related quality of life (HRQoL) in patients with psoriatic arthritis (PsA).
In this multicenter, double-blind, placebo-controlled, crossover study of ustekinumab, patients with active PsA were randomized (1:1 ratio) to receive either ustekinumab at weeks 0, 1, 2, and 3 and placebo at weeks 12 and 16 (n = 76) or placebo at weeks 0, 1, 2, and 3 and ustekinumab at weeks 12 and 16 (n = 70). Physical function was assessed using the disability index from the Health Assessment Questionnaire-Disability Index (HAQ-DI) in all randomized patients. HRQoL was evaluated using the Dermatology Life Quality Index (DLQI) in a subset of patients (84.9%) with at least 3% body surface area (BSA) psoriasis involvement at baseline.
At baseline, overall mean HAQ-DI and DLQI scores were 0.9 and 11.5, respectively, indicating impaired physical function and moderate effect on HRQoL. At week 12, ustekinumab patients had significantly more improvement (decrease) in the mean HAQ-DI (-0.31) and DLQI (-8.6) scores versus placebo (-0.04 and -0.8, respectively; p < 0.001 for both comparisons). At week 12, 58.7% (37/63) of ustekinumab-treated patients had a DLQI score of 0 or 1 (no negative effect of disease or treatment on HRQoL) versus 5.5% (3/55) for placebo (p < 0.001). The results also indicated a positive but weak correlation between improvement in physical function and HRQoL, pain, and skin response as well as between improvement in joint and skin responses in patients receiving ustekinumab or placebo. Potential limitations of the study include the short duration of the placebo-controlled period and the relatively small patient population.
Ustekinumab significantly improved physical function and HRQoL in patients with PsA and psoriasis involving at least 3% BSA.
利用一项 II 期临床试验的数据,评估 ustekinumab(一种与人白细胞介素-12 和 -23 的共享 p40 亚单位高亲和力结合的人免疫球蛋白单克隆抗体)对患有银屑病关节炎(PsA)的患者的身体残疾和健康相关生活质量(HRQoL)的影响。
在这项多中心、双盲、安慰剂对照、交叉研究中,接受 ustekinumab 治疗的活动期 PsA 患者按照 1:1 的比例随机分配(n = 76),分别在第 0、1、2 和 3 周接受 ustekinumab 治疗,在第 12 和 16 周接受安慰剂治疗;或在第 0、1、2 和 3 周接受安慰剂治疗,在第 12 和 16 周接受 ustekinumab 治疗(n = 70)。在所有随机患者中,使用健康评估问卷残疾指数(HAQ-DI)评估身体功能。在基线时有至少 3%的体表面积(BSA)银屑病受累的患者亚组(84.9%)中,使用皮肤病生活质量指数(DLQI)评估 HRQoL。
基线时,总体平均 HAQ-DI 和 DLQI 评分分别为 0.9 和 11.5,表明身体功能受损和对 HRQoL 的中度影响。在第 12 周时,与安慰剂相比,ustekinumab 治疗的患者 HAQ-DI(-0.31)和 DLQI(-8.6)评分的平均改善程度更大(分别为-0.04 和-0.8;两者均 p < 0.001)。在第 12 周时,58.7%(37/63)的 ustekinumab 治疗患者的 DLQI 评分为 0 或 1(疾病或治疗对 HRQoL 无负面影响),而安慰剂组为 5.5%(3/55)(p < 0.001)。结果还表明,接受 ustekinumab 或安慰剂治疗的患者的身体功能和 HRQoL、疼痛和皮肤反应的改善之间存在正相关关系,但相关性较弱,关节和皮肤反应的改善之间也存在正相关关系。研究的潜在局限性包括安慰剂对照期的持续时间短和患者人群相对较小。
Ustekinumab 显著改善了至少有 3%BSA 受累的银屑病关节炎和银屑病患者的身体功能和 HRQoL。