Etanercept monotherapy in patients with psoriasis: A summary of safety, based on an integrated multistudy database

被引:57
作者
Gottlieb, AB
Leonardi, CL
Goffe, BS
Ortonne, JP
van der Kerkhof, PCM
Zitnik, R
Nakanishi, A
Jahreis, A
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Clin Res Ctr, New Brunswick, NJ 08901 USA
[2] St Louis Univ, Sch Med, St Louis, MO 63103 USA
[3] Dermatol Associates, Seattle, WA USA
[4] CHU Hosp, Nice, France
[5] Univ St Radboud, Med Ctr, Nijmegen, Netherlands
[6] Amgen Inc, Thousand Oaks, CA 91320 USA
关键词
D O I
10.1016/j.jaad.2005.10.053
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 tumor necrosis factor antagonist, is an approved treatment in the United States and Europe for plaque psoriasis. Objective: To further examine the safety profile of etanercept in patients with chronic, moderate to severe plaque psoriasis. Methods: Safety data from an integrated database of 1347 patients from 3 randomized, double-blind, placebo-controlled clinical trials were analyzed. Safety end points included incidence rates of adverse events, serious adverse events, infections, serious infections, injection site reactions, and routine laboratory assessments. Pooled safety results from the first 12 weeks of each trial are reported here. Results: Rates of adverse events, serious adverse events, infections, and serious infections in the first 12 weeks of the 3 trials were similar among all active groups as well as each active group, compared with the placebo group. No dose-related toxicities were reported. Limitations: This report includes a relatively short (12-week) time frame; data from patients exposed to etanercept for longer periods are needed. Conclusions: Etanercept was generally safe in a large cohort of patients with moderate to severe plaque psoriasis.
引用
收藏
页码:S92 / S100
页数:9
相关论文
共 34 条
[1]   Disease activity and risk of lymphoma in patients with rheumatoid arthritis:: nested case-control study [J].
Baecklund, E ;
Ekbom, A ;
Sparén, P ;
Feltelius, N ;
Klareskog, L .
BRITISH MEDICAL JOURNAL, 1998, 317 (7152) :180-181
[2]   Methotrexate for psoriasis [J].
Boffa, MJ ;
Chalmers, RJG .
CLINICAL AND EXPERIMENTAL DERMATOLOGY, 1996, 21 (06) :399-408
[3]   Cancer risk in a population-based cohort of patients hospitalized for psoriasis in Sweden [J].
Boffetta, P ;
Gridley, G ;
Lindelöf, B .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2001, 117 (06) :1531-1537
[4]   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
[5]  
Culy CR, 2002, DRUGS, V62, P2493
[6]   Infections and biological therapy in rheumatoid arthritis [J].
Cunnane, G ;
Doran, M ;
Bresnihan, B .
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2003, 17 (02) :345-363
[7]   SEVERE PSORIASIS - ORAL THERAPY WITH A NEW RETINOID [J].
FREDRIKSSON, T ;
PETTERSSON, U .
DERMATOLOGICA, 1978, 157 (04) :238-244
[8]   The role of PUVA in the treatment of psoriasis: Photobiology issues related to skin cancer incidence [J].
Gasparro F.P. .
American Journal of Clinical Dermatology, 2000, 1 (6) :337-348
[9]   Lymphoma rates are low but increased in patients with psoriasis - Results from a population-based cohort study in the United Kingdom [J].
Gelfand, JM ;
Berlin, J ;
Van Voorhecs, A ;
Margolis, DJ .
ARCHIVES OF DERMATOLOGY, 2003, 139 (11) :1425-1429
[10]   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