Griffiths Christopher Em, Stein Gold Linda, Cambazard Frédéric, Kalb Robert E, Lowson David, Møller Anders, Paul Carle
Dermatology Centre, Salford Royal Hospital, University of Manchester, Manchester, UK.
Henry Ford Health System, Detroit, MI, USA.
Eur J Dermatol. 2018 Jun 1;28(3):356-363. doi: 10.1684/ejd.2018.3302.
Health-related quality of life (HRQoL) measures provide patient-centred evaluations of response to treatment. In the 12-week, Phase III PSO-ABLE study, fixed-combination calcipotriol 50 μg/g as hydrate (Cal) plus betamethasone 0.5 mg/g as dipropionate (BD) aerosol foam was significantly more effective for the treatment of psoriasis than Cal/BD gel.
To compare HRQoL in mild-severe psoriasis vulgaris patients (involving 2-30% body surface area) over 12 weeks of treatment with Cal/BD foam or gel.
HRQoL was assessed using: Dermatology Life Quality Index (DLQI), EuroQoL-5D-5L-PSO (EQ-5D), and Psoriasis QoL (PQoL-12) questionnaires (baseline, Weeks 4, 8 and 12); DLQI score of 0/1 (range: 0-30) and weighted EQ-5D utility index score of 1 (range: 0-1) indicates there is no impact on a patient's QoL and perfect health, respectively. Itch, itch-related sleep loss, and work impairment were also assessed.
In total, 463 patients were randomized to the study (Cal/BD foam, n = 185; Cal/BD gel, n = 188; foam vehicle, n = 47; gel vehicle, n = 43). Significantly more Cal/BD foam patients achieved DLQI scores of 0/1 at Weeks 4 (45.7% vs 32.4%; p = 0.013) and 12 (60.5% vs 44.1%; p = 0.003) than Cal/BD gel patients. Cal/BD foam significantly improved EQ-5D utility index (0.09 vs 0.03; p<0.001) and PQoL-12 scores (-2.23 vs -2.07; p = 0.029) from baseline to Week 4 versus Cal/BD gel. Itch, itch-related sleep loss, and work impairment improved more with Cal/BD foam than gel.
Cal/BD foam demonstrated greater HRQoL improvement in patients with psoriasis than Cal/BD gel over 12 weeks of treatment.
健康相关生活质量(HRQoL)测量可提供以患者为中心的治疗反应评估。在为期12周的III期PSO-ABLE研究中,与卡泊三醇/倍他米松凝胶相比,50μg/g水合物形式的卡泊三醇(Cal)加0.5mg/g二丙酸倍他米松(BD)的固定组合气雾剂泡沫对银屑病的治疗效果显著更佳。
比较寻常型轻至重度银屑病患者(体表面积累及2%-30%)在使用卡泊三醇/倍他米松泡沫或凝胶治疗12周期间的健康相关生活质量。
使用以下问卷评估健康相关生活质量:皮肤病生活质量指数(DLQI)、欧洲五维健康量表-5维度-5水平-银屑病(EQ-5D)和银屑病生活质量问卷(PQoL-12)(基线、第4周、第8周和第12周);DLQI评分为0/1(范围:[0-30])和加权EQ-5D效用指数评分为1(范围:[0-1])分别表示对患者生活质量无影响和健康状况完美。还评估了瘙痒、与瘙痒相关的睡眠障碍和工作障碍。
总共463名患者被随机分配至该研究(卡泊三醇/倍他米松泡沫组,n = 185;卡泊三醇/倍他米松凝胶组,n = 188;泡沫赋形剂组,n = 47;凝胶赋形剂组,n = 43)。与卡泊三醇/倍他米松凝胶组患者相比,显著更多的卡泊三醇/倍他米松泡沫组患者在第4周(45.7%对32.4%;p = 0.013)和第12周(60.5%对44.1%;p = 0.003)达到DLQI评分为0/1。从基线至第4周,与卡泊三醇/倍他米松凝胶相比,卡泊三醇/倍他米松泡沫显著改善了EQ-5D效用指数(0.09对-0.03;p<0.001)和PQoL-12评分(-2.23对-2.07;p = 0.029)。与凝胶相比,卡泊三醇/倍他米松泡沫在改善瘙痒、与瘙痒相关的睡眠障碍和工作障碍方面效果更佳。
在12周的治疗期间,与卡泊三醇/倍他米松凝胶相比,卡泊三醇/倍他米松泡沫在银屑病患者中显示出更大的健康相关生活质量改善。