Etanercept

被引:39
作者
Ducharme, Erin [1 ]
Weinberg, Jeffrey M. [1 ]
机构
[1] St Lukes Roosevelt Hosp, Dept Dermatol, New York, NY 10025 USA
关键词
cytokine; etanercept; off-label; psoriasis; psoriatic arthritis; tumor necrosis factor;
D O I
10.1517/14712598.8.4.491
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: In some patients with psoriasis the inflammatory process fueling skin lesions also afflicts their joints in a condition called psoriatic arthritis. TNF-alpha has been shown to play a central role in the pathogenesis of both cutaneous and joint disease. Etanercept is a soluble fusion protein that binds TNF-alpha, rendering the molecule inactive and making etanercept an effective, targeted therapeutic option for many TNF-mediated inflammatory diseases. Objective: To review the key clinical trials which evaluated efficacy of etanercept for the treatment of psoriasis and psoriatic arthritis, discuss various off-label uses for this therapeutic agent and describe the adverse events associated with its use. Methods: A search of Medline for relevant articles on etanercept and psoriasis. Results/conclusion: Etanercept has demonstrated efficacy in the treatment of skin and joint manifestations of psoriatic disease, thus gaining FDA approval for use in both. A growing number of off-label dermatological uses for etanercept have been proposed, with variable success reported in individual cases or small series. Since its introduction little over a decade ago, etanercept has maintained a favorable safety profile.
引用
收藏
页码:491 / 502
页数:12
相关论文
共 85 条
[1]   Aggressive cutaneous T-cell lymphomas after TNFα blockade [J].
Adams, AE ;
Zwicker, J ;
Curiel, C ;
Kadin, ME ;
Falchuk, KR ;
Drews, R ;
Kupper, TS .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2004, 51 (04) :660-662
[2]   Treatment of refractory Churg-Strauss-Syndrome (CSS) by TNF-α blockade [J].
Arbach, O ;
Gross, WL ;
Gause, A .
IMMUNOBIOLOGY, 2002, 206 (05) :496-501
[3]  
Berookhim B, 2004, CUTIS, V74, P245
[4]   Anti-TNF antibody therapy in rheumatoid arthritis and the risk of serious infections and malignancies - Systematic review and meta-analysis of rare harmful effects in randomized controlled trials [J].
Bongartz, T ;
Sutton, AJ ;
Sweeting, MJ ;
Buchan, I ;
Matteson, EL ;
Montori, V .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (19) :2275-2285
[5]   Cytokines in psoriasis [J].
Bonifati, C ;
Ameglio, F .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 1999, 38 (04) :241-251
[6]   CORRELATED INCREASES OF TUMOR-NECROSIS-FACTOR-ALPHA, INTERLEUKIN-6 AND GRANULOCYTE-MONOCYTE COLONY-STIMULATING FACTOR LEVELS IN SUCTION BLISTER FLUIDS AND SERA OF PSORIATIC PATIENTS - RELATIONSHIPS WITH DISEASE SEVERITY [J].
BONIFATI, C ;
CARDUCCI, M ;
FEI, PC ;
TRENTO, E ;
SACERDOTI, G ;
FAZIO, M ;
AMEGLIO, F .
CLINICAL AND EXPERIMENTAL DERMATOLOGY, 1994, 19 (05) :383-387
[7]   The PREMIER study - A multicenter, randomized, double-blind clinical trial of combination therapy with adalimumab plus methotrexate versus methotrexate alone or adalimumab alone in patients with early, aggressive rheumatoid arthritis who had not had previous methotrexate treatment [J].
Breedveld, FC ;
Weisman, MH ;
Kavanaugh, AF ;
Cohen, SB ;
Pavelka, K ;
van Vollenhoven, R ;
Sharp, J ;
Perez, JL ;
Spencer-Green, GT .
ARTHRITIS AND RHEUMATISM, 2006, 54 (01) :26-37
[8]   Infection complications associated with the use of biologic agents [J].
Bresnihan, B ;
Cunnane, G .
RHEUMATIC DISEASE CLINICS OF NORTH AMERICA, 2003, 29 (01) :185-+
[9]   Tumor necrosis factor antagonist therapy and lymphoma development - Twenty-six cases reported to the Food and Drug Administration [J].
Brown, SL ;
Greene, MH ;
Gershon, SK ;
Edwards, ET ;
Braun, MM .
ARTHRITIS AND RHEUMATISM, 2002, 46 (12) :3151-3158
[10]  
Callegari PE, 2006, JAMA-J AM MED ASSOC, V296, P2202, DOI 10.1001/jama.296.18.2202