A randomized comparison of continuous vs. intermittent infliximab maintenance regimens over 1 year in the treatment of moderate-to-severe plaque psoriasis

被引:390
作者
Menter, Alan
Feldman, Steven R.
Weinstein, Gerald D.
Papp, Kim
Evans, Robert
Guzzo, Cynthia
Li, Shu
Dooley, Lisa T.
Arnold, Cynthia
Gottlieb, Alice B.
机构
[1] Baylor Univ, Med Ctr, UT SW Med Sch, Div Dermatol, Dallas, TX 75230 USA
[2] Wake Forest Univ, Sch Med, Winston Salem, NC 27109 USA
[3] Univ Calif Irvine, Irvine, CA USA
[4] Prob Res, Waterloo, ON, Canada
[5] Scios Inc, Fremont, CA USA
[6] Centocor Inc, Malvern, PA 19355 USA
[7] Tufts Univ New England Med Ctr, Dept Dermatol, Boston, MA USA
关键词
D O I
10.1016/j.jaad.2006.07.017
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Previous studies of infliximab) in psoriasis have demonstrated rapid improvement with induction therapy and sustained response with regularly administered maintenance therapy. Objective: The efficacy and safety of continuous (every-8-week) and intermittent (as-needed) maintenance regimens were compared. Methods: Patients with moderate-to-severe psoriasis (n = 835) were randomized to induction therapy (weeks 0, 2, and 6) with infliximab 3 mg/kg or 5 mg/kg or placebo. Infliximab-treated patients were randomized again at week 14 to continuous or intermittent maintenance regimens at their induction close. Results: At week 10, 75.5% and 70.3% of patients in the infliximab 5 mg/kg and 3 mg/kg groups, respectively, achieved PASI 75; 45.2% and 37.1% achieved PASI 90 (vs 1.9% [PASI 75] and 0.5% [PASI 901 for placebo; P <.001). Through week 50, PASI responses were better maintained with continuous compared with intermittent therapy within each close, and with 5 mg/kg compared with 3 mg/kg continuous therapy. Limitations: Longer term (>1 year) maintenance therapy and further study Of infliximab serum concentrations over this period, in both PASI 75 responders and non-responders, would he preferable. Conclusions: Through week 50, response was hest maintained with continuous infliximab therapy. Infliximab was generally well-tolerated in most patients.
引用
收藏
页码:31 / 44
页数:14
相关论文
共 32 条
[11]   Current severe psoriasis and the Rule of Tens [J].
Finlay, AY .
BRITISH JOURNAL OF DERMATOLOGY, 2005, 152 (05) :861-867
[12]   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
[13]   SEVERE PSORIASIS - ORAL THERAPY WITH A NEW RETINOID [J].
FREDRIKSSON, T ;
PETTERSSON, U .
DERMATOLOGICA, 1978, 157 (04) :238-244
[14]   Innate and adaptive immunity and the pathophysiology of psoriasis [J].
Gaspari, AA .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2006, 54 (03) :S67-S80
[15]  
*GEN INC, 2005, RAPT PACK INS
[16]   Infliximab induction therapy for patients with severe plaque-type psoriasis: A randomized, double-blind, placebo-controlled trial [J].
Gottlieb, AB ;
Evans, R ;
Li, S ;
Dooley, LT ;
Guzzo, CA ;
Baker, D ;
Bala, M ;
Marano, CW ;
Menter, A .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2004, 51 (04) :534-542
[17]   Incidence and Importance of Antibody Responses to Infliximab After Maintenance or Episodic Treatment in Crohn's Disease [J].
Hanauer, Stephen B. ;
Wagner, Carrie L. ;
Bala, Mohan ;
Mayer, Lloyd ;
Travers, Suzanne ;
Diamond, Robert H. ;
Olson, Allan ;
Bao, Warren ;
Rutgeerts, Paul .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2004, 2 (07) :542-553
[18]  
KIMBALL AB, 2004, AM AC DERM SUMM M PR
[19]  
KRISTENSEN M, 1993, CLIN EXP IMMUNOL, V94, P354
[20]   Potential of tumor necrosis factor inhibitors in psoriasis and psoriatic arthritis [J].
Krueger, G ;
Callis, K .
ARCHIVES OF DERMATOLOGY, 2004, 140 (02) :218-225