Patient-reported outcomes of psoriasis improvement with etanercept therapy: results of a randomized phase III trial

被引:111
作者
Krueger, GG
Langley, RG
Finlay, AY
Griffiths, CEM
Woolley, JM
Lalla, D
Jahreis, A
机构
[1] Univ Utah, Hlth Sci Ctr, Dept Dermatol, Salt Lake City, UT 84132 USA
[2] Dalhousie Univ, QE2 Hlth Sci Ctr, Halifax, NS B3H 1V8, Canada
[3] Univ Cardiff Wales, Hope Hosp, Dermatol Ctr, Cardiff CF14 4XN, Wales
[4] Amgen Inc, Thousand Oaks, CA 91320 USA
关键词
etanercept; patient-reported outcomes; psoriasis; quality of life; randomized controlled trial; tumour necrosis factor;
D O I
10.1111/j.1365-2133.2005.06948.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Etanercept, a soluble tumour necrosis factor receptor, lessens the severity of psoriasis as measured by physician-reported clinical outcomes. Equally important is the patient perspective on the effect of etanercept therapy on daily life. Objectives To assess patient-reported outcomes (PROs) in patients with psoriasis receiving etanercept therapy. Methods In this multinational, randomized, phase III trial, patients with psoriasis received placebo (n = 193), etanercept 50 mg per week (n = 196) or etanercept 50 mg twice weekly (n = 194) during the initial 12-week, double-blind period. Thereafter, all patients received open-label etanercept (50 mg per week). The following PROs were assessed: Dermatology Life Quality Index (DLQI), Short Form-36 Health Survey (SF-36), patient rating of pruritus, and patient global assessment of psoriasis. Results At week 12, DLQI total score improved by 65-70% in patients receiving etanercept compared with 6% in patients receiving placebo (P < 0.0001), and improvement in DLQI was clinically meaningful (>= 5-point improvement or 0 score) for 72-77% of patients receiving etanercept therapy. All DLQI and SF-36 subscales and the SF-36 physical and mental component summary scores demonstrated significantly greater improvement with etanercept therapy than with placebo, illustrating that etanercept benefits patients with psoriasis across multiple domains that contribute to health-related quality of life. With etanercept therapy, distributions of patient ratings of pruritus and global assessment of disease shifted from moderate to severe (baseline) to minimal to good (week 12). Etanercept-induced benefits of PROs were maintained for patients who reduced their dose after 12 weeks. Conclusions Etanercept therapy improves PROs in patients with psoriasis and makes a meaningful difference to their lives. These results support the efficacy profile of physician-reported clinical measures while providing a more complete understanding of the benefits experienced by patients with psoriasis treated with etanercept.
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页码:1192 / 1199
页数:8
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