Efficacy of Systemic Treatments for Moderate to Severe Plaque Psoriasis: Systematic Review and Meta-Analysis

被引:74
作者
Bansback, Nick [2 ]
Sizto, Sonia [2 ]
Sun, Huiying [2 ]
Feldman, Steven [3 ,4 ,5 ]
Willian, Mary Kaye [6 ]
Anis, Aslam [1 ,2 ]
机构
[1] Univ British Columbia, Fac Med, Sch Populat & Publ Hlth, Vancouver, BC V6T 1Z3, Canada
[2] St Pauls Hosp, Ctr Hlth Evaluat & Outcome Sci, Vancouver, BC V6Z 1Y6, Canada
[3] Wake Forest Univ, Bowman Gray Sch Med, Dept Dermatol, Winston Salem, NC 27103 USA
[4] Wake Forest Univ, Bowman Gray Sch Med, Dept Pathol, Winston Salem, NC 27103 USA
[5] Wake Forest Univ, Bowman Gray Sch Med, Dept Publ Hlth Sci, Winston Salem, NC 27103 USA
[6] Abbott Labs, Abbott Pk, IL 60064 USA
关键词
Biologics; Meta-analysis; Psoriasis; Randomized controlled trial; Systematic review; TO-SEVERE PSORIASIS; RANDOMIZED CONTROLLED-TRIAL; MIXED TREATMENT COMPARISONS; PHASE-III; DOUBLE-BLIND; CLINICAL-RESPONSE; INFLIXIMAB INDUCTION; BIOLOGICAL THERAPIES; ETANERCEPT; EFALIZUMAB;
D O I
10.1159/000233234
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
Aims: To compare the efficacy of psoriasis treatments through a systematic literature review and meta-analysis. Methods: Randomized controlled trials evaluating the Psoriasis Area and Severity Index (PASI) were identified and assessed for quality. PASI responses were modeled using a mixed-treatment comparison, which enabled the estimation of the relative effectiveness of several treatments. Sensitivity analyses were performed. Results: Twenty-two trials were included. Tumor necrosis factor (TNF) inhibitors were most likely to achieve PASI 75, with a mean relative risk (RR) of 15.57 (95% CI 12.46-19.25) versus mean RRs of 9.24 (95% CI 5.33-13.91) for systemic and 5.65 (95% CI 3.74-7.97) for T-cell therapies. Infliximab (81%) and adalimumab (71%) had greater probabilities of achieving PASI 75 than etanercept (50%). Dosage was an important determinant of outcome. Conclusions: TNF inhibitors were more effective than T cell agents; adalimumab and infliximab were more effective than systemic therapies and etanercept. Evidence-based comparisons support patient and physician decisions. Copyright (C) 2009 S. Karger AG, Basel
引用
收藏
页码:209 / 218
页数:10
相关论文
共 44 条
[1]
Confidence intervals for the number needed to treat [J].
Altman, DG .
BRITISH MEDICAL JOURNAL, 1998, 317 (7168) :1309-1312
[2]
[Anonymous], GUID METH TECHN APPR
[3]
Ashcroft DM, 1999, BRIT J DERMATOL, V141, P185
[4]
Safety and efficacy of alefacept, efalizumab, etanercept and infliximab in treating moderate to severe plaque psoriasis: a meta-analysis of randomized controlled trials [J].
Brimhall, A. K. ;
King, L. N. ;
Licciardone, J. C. ;
Jacobe, H. ;
Menter, A. .
BRITISH JOURNAL OF DERMATOLOGY, 2008, 159 (02) :274-285
[5]
Efficacy and safety of infliximab monotherapy for plaque-type psoriasis: a randomised trial [J].
Chaudhari, U ;
Romano, P ;
Mulcahy, LD ;
Dooley, LT ;
Baker, DG ;
Gottlieb, AB .
LANCET, 2001, 357 (9271) :1842-1847
[6]
Clinical experience acquired with the efalizumab (Raptiva®) (CLEAR) trial in patients with moderate-to-severe plaque psoriasis:: results from a phase III international randomized, placebo-controlled trial [J].
Dubertret, L. ;
Sterry, W. ;
Bos, J. D. ;
Chimenti, S. ;
Shumack, S. ;
Larsen, C. G. ;
Shear, N. H. ;
Papp, K. A. .
BRITISH JOURNAL OF DERMATOLOGY, 2006, 155 (01) :170-181
[7]
Treatment of chronic plaque psoriasis by selective targeting of memory effector T lymphocytes [J].
Ellis, CN ;
Krueger, GG .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (04) :248-255
[8]
SEVERE PSORIASIS - ORAL THERAPY WITH A NEW RETINOID [J].
FREDRIKSSON, T ;
PETTERSSON, U .
DERMATOLOGICA, 1978, 157 (04) :238-244
[9]
Efalizumab for patients with moderate to severe plaque psoriasis - A randomized controlled trial [J].
Gordon, KB ;
Papp, KA ;
Hamilton, TK ;
Walicke, PA ;
Dummer, W ;
Li, N ;
Bresnahan, BW ;
Menter, A .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (23) :3073-3080
[10]
Clinical response to alimumab treatment in patients with moderate to severe psoriasis: Double-blind, randomized controlled trial and open-label extension study [J].
Gordon, Kenneth B. ;
Langley, Richard G. ;
Leonardi, Craig ;
Toth, Darryl ;
Menter, M. Alan ;
Kang, Sewon ;
Heffernan, Michael ;
Miller, Bruce ;
Hamlin, Regina ;
Lim, Liberata ;
Zhong, Jianhua ;
Hoffman, Rebecca ;
Okun, Martin M. .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2006, 55 (04) :598-606