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Area and Severity Index (PASI) 75 at weeks 28 and 40 were re-randomized at week 40 to continue ustekinumab or be withdrawn until loss of therapeutic effect.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
相关论文
共 38 条
[1]  
[Anonymous], Psoriasis Statistics
[2]   Getting under the skin: The immunogenetics of psoriasis [J].
Bowcock, AM ;
Krueger, JG .
NATURE REVIEWS IMMUNOLOGY, 2005, 5 (09) :699-711
[3]  
De Arruda LHF, 2001, BRIT J DERMATOL, V144, P33, DOI 10.1046/j.1365-2133.2001.00034.x
[4]   Infliximab treatment results in significant improvement in the quality of life of patients with severe psoriasis: a double-blind placebo-controlled trial [J].
Feldman, SR ;
Gordon, KB ;
Bala, M ;
Evans, R ;
Li, S ;
Dooley, LT ;
Guzzo, C ;
Patel, K ;
Menter, A ;
Gottlieb, AB .
BRITISH JOURNAL OF DERMATOLOGY, 2005, 152 (05) :954-960
[5]   Improved health-related quality of life following a randomized controlled trial of alefacept treatment in patients with chronic plaque psoriasis [J].
Feldman, SR ;
Menter, A ;
Koo, JY .
BRITISH JOURNAL OF DERMATOLOGY, 2004, 150 (02) :317-326
[6]   DERMATOLOGY LIFE QUALITY INDEX (DLQI) - A SIMPLE PRACTICAL MEASURE FOR ROUTINE CLINICAL USE [J].
FINLAY, AY ;
KHAN, GK .
CLINICAL AND EXPERIMENTAL DERMATOLOGY, 1994, 19 (03) :210-216
[7]  
Fortune DG, 1997, BRIT J DERMATOL, V137, P755
[8]   SEVERE PSORIASIS - ORAL THERAPY WITH A NEW RETINOID [J].
FREDRIKSSON, T ;
PETTERSSON, U .
DERMATOLOGICA, 1978, 157 (04) :238-244
[9]   Prevalence and treatment of psoriasis in the United Kingdom - A population-based study [J].
Gelfand, JM ;
Weinstein, R ;
Porter, SB ;
Neimann, AL ;
Berlin, JA ;
Margolis, D .
ARCHIVES OF DERMATOLOGY, 2005, 141 (12) :1537-1541
[10]   Ustekinumab, a human interleukin 12/23 monoclonal antibody, for psoriatic arthritis: randomised, double-blind, placebo-controlled, crossover trial [J].
Gottlieb, Alice ;
Menter, Alan ;
Mendelsohn, Alan ;
Shen, Yaung-Kaung ;
Li, Shu ;
Guzzo, Cynthia ;
Fretzin, Scott ;
Kunynetz, Rod ;
Kavanaugh, Arthur .
LANCET, 2009, 373 (9664) :633-640