Drugs that block tumour necrosis factor: Experience in patients with rheumatoid arthritis

被引:39
作者
Moreland, LW [1 ]
机构
[1] Univ Alabama Birmingham, Dept Med, Div Clin Immunol & Rheumatol, Birmingham, AL 35294 USA
关键词
D O I
10.2165/00019053-200422001-00005
中图分类号
F [经济];
学科分类号
02 ;
摘要
Three biological response modifiers that inhibit tumour necrosis factor-alpha (TNF-alpha) are approved for treating rheumatoid arthritis (RA). Etanercept is a fusion protein comprising two soluble human TNF-alpha receptors linked to the Fc fragment of human immunoglobulin G(1). Infliximab is a chimeric (human/mouse) monoclonal antibody and adalimumab is a humanised monoclonal antibody. In placebo-controlled trials in established disease-modifying antirheumatic drug (DMARD)-refractory RA, the anti-TNF-alpha agents have reduced disease activity, as monotherapy or in combination with methotrexate. In long-term, open-label studies with etanercept or adalimumab, clinical response was sustained for up to 5 years. In early RA, etanercept has similar efficacy to methotrexate. However, etanercept was more effective than methotrexate in preventing radiographic progression. Preventing or delaying disease progression and disability with etanercept therapy in early RA may reduce costs associated with long-term disease outcomes. Data also suggest a benefit of infliximab plus methotrexate or adalimumab plus methotrexate in early RA. All three agents have been shown to improve functionality as assessed by health assessment questionnaire (HAQ) disability scores. Health-related quality of life is also improved in terms of physical and mental health and vitality. Furthermore, etanercept and adalimumab are associated with a reduction in fatigue. Long-term etanercept or infliximab therapy is associated with increased job employment and etanercept also reduces healthcare utilisation. Mild, transient injection-site reactions occur in about 33% of patients treated with etanercept and 20% of patients treated with adalimumab. In patients treated with infliximab, 16-20% have infusion reactions. The incidence of serious infection associated with etanercept and infliximab was low, about 2-3% in etanercept studies of up to 5 years duration, and 5% in a survey of more than 10 infliximab trials. This paper reviews the evidence for efficacy, safety and effectiveness of anti-TNF-alpha agents in RA.
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页码:39 / 53
页数:15
相关论文
共 98 条
[1]  
*ABB LAB, 2003, ABB HUM ADAL PRESCR
[2]   Treatment strategy, disease activity, and outcome in four cohorts of patients with early rheumatoid arthritis [J].
Albers, JMC ;
Paimela, L ;
Kurki, P ;
Eberhardt, KB ;
Emery, P ;
van't Hof, MA ;
Schreuder, FHJM ;
Leirisalo-Repo, M ;
van Riel, PLCM .
ANNALS OF THE RHEUMATIC DISEASES, 2001, 60 (05) :453-458
[3]  
ANTONI C, 1999, ANN RHEUM DIS, V217, P6
[4]  
Antoni CE, 2001, ARTHRITIS RHEUM, V44, pS84
[5]   Drug survival, efficacy and toxicity of monotherapy with a fully human anti-tumour necrosis factor-α antibody compared with methotrexate in long-standing rheumatoid arthritis [J].
Barrera, P ;
van der Maas, A ;
van Ede, AE ;
Kiemeney, BALM ;
Laan, RFJM ;
van de Putte, LBA ;
van Riel, PLCM .
RHEUMATOLOGY, 2002, 41 (04) :430-439
[6]   A comparison of etanercept and methotrexate in patients with early rheumatoid arthritis [J].
Bathon, JM ;
Martin, RW ;
Fleischmann, RM ;
Tesser, JR ;
Schiff, MH ;
Keystone, EC ;
Genovese, MC ;
Wasko, MC ;
Moreland, LW ;
Weaver, AL ;
Markenson, J ;
Finck, BK .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (22) :1586-1593
[7]  
Baumgartner S, 2001, J RHEUMATOL, V28, P106
[8]  
BAURNGARTNER S, 2001, J RHEUMATOL S63, V28, P106
[9]  
BREEDVELD F, 2002, J CLIN RHEUM S3, V8, P46
[10]  
Burge DJ, 2001, J RHEUMATOL, V28, P106