Ustekinumab improves health-related quality of life in patients with moderate-to-severe psoriasis: results from the PHOENIX 1 trial

被引:80
作者
Lebwohl, M. [2 ]
Papp, K. [3 ,4 ]
Han, C. [5 ]
Schenkel, B. [5 ]
Yeilding, N. [6 ]
Wang, Y. [6 ]
Krueger, G. G. [1 ]
机构
[1] Univ Utah, Salt Lake City, UT 84132 USA
[2] Mt Sinai Sch Med, New York, NY USA
[3] Univ Western Ontario, London, ON, Canada
[4] Prob Med Res, Waterloo, ON, Canada
[5] Johnson & Johnson Pharmaceut Sci LLC, Worldwide Hlth Econ, Horsham, PA USA
[6] Centocor Res & Dev Inc, Malvern, PA USA
关键词
Dermatology Life Quality Index; health-related quality of life; interleukin-12; 23; psoriasis; SF-36; ustekinumab; INTERLEUKIN-12/23; MONOCLONAL-ANTIBODY; DOUBLE-BLIND; BIOLOGICAL THERAPIES; INDEX; EFFICACY; BURDEN; IMPACT; SAFETY; SKIN;
D O I
10.1111/j.1365-2133.2009.09491.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
P>Background PHOENIX 1 was a phase III, randomized, double-blind, placebo-controlled study that demonstrated the long-term efficacy and safety of ustekinumab in patients with moderate-to-severe psoriasis. Objectives To assess the effect of ustekinumab maintenance therapy on health-related quality of life (HRQoL) in PHOENIX 1 patients. Patients and methods Patients (n = 766) were randomized to receive ustekinumab 45 mg (n = 255) or 90 mg (n = 256) at weeks 0 and 4 and every 12 weeks thereafter, or placebo (n = 255) at weeks 0 and 4 with crossover to ustekinumab at week 12. Ustekinumab-randomized patients achieving at least 75% improvement in Psoriasis Area and Severity Index (PASI) 75 at weeks 28 and 40 were re-randomized at week 40 to continue ustekinumab or be withdrawn until loss of therapeutic effect. HRQoL was assessed using the SF-36 and Dermatology Life Quality Index (DLQI). Results At baseline, more than 97% had a DLQI > 1 and the average DLQI was > 10, indicating a significant impact on patients' HRQoL. Significantly greater proportions of patients receiving ustekinumab 45 and 90 mg achieved a normalized DLQI score (< 1) compared with placebo (53 center dot 2%, 52 center dot 4% and 6 center dot 0%, respectively, both P < 0 center dot 001) at week 12 and achieved a clinically meaningful improvement (increase of at least five points) in SF-36 physical (23 center dot 1%, 33 center dot 7% and 15 center dot 6%) and mental (25 center dot 5%, 31 center dot 3% and 14 center dot 8%) component summary scores. At week 12, changes in individual DLQI and SF-36 domains were significantly better in each ustekinumab group vs. placebo (P < 0 center dot 001). The magnitude of improvement across SF-36 scales was greatest for the bodily pain and social functioning domains. Improvements in HRQoL were sustained with maintenance ustekinumab therapy through at least 1 year. Regression analysis showed that, after adjustment for improvement in PASI or Physician's Global Assessment (PGA), ustekinumab-treated patients demonstrated significant improvements in DLQI. Conclusions Ustekinumab improves HRQoL in patients with moderate-to-severe psoriasis. Patient-reported outcomes measured a treatment effect beyond that indicated by clinical measures.
引用
收藏
页码:137 / 146
页数:10
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