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Annals of the Rheumatic Diseases 2006;65:701-703; doi:10.1136/ard.2005.049890
Copyright © 2006 BMJ Publishing Group Ltd & European League Against Rheumatism.

EDITORIAL

Rheumatoid arthritis

Differential drug resistance to anti-tumour necrosis factor agents in rheumatoid arthritis

P I Sidiropoulos, D T Boumpas

Departments of Internal Medicine and Rheumatology, Clinical Immunology and Allergy, University of Crete, University Hospital, Voutes 71110 Heraklion, Greece

Correspondence to:
Correspondence to:
Professor D T Boumpas
boumpasd@med.uoc.gr


A significant number of patients receiving infliximab require dosing adjustments while some patients may indeed develop drug resistance

Keywords: rheumatoid arthritis; anti-tumour necrosis factor agents; drug resistance; antirheumatic therapy

The first 150 words of the full text of this article appear below.

Rheumatoid arthritis (RA) is a chronic, inflammatory autoimmune disease that leads to progressive joint destruction and disability. New biological drugs have been added to our armamentarium since 1999, including agents targeting tumour necrosis factor {alpha} (TNF{alpha}). Among them, infliximab, etanercept, and adalimumab in randomised controlled trials (RCTs), reduced signs and symptoms of RA and protected joints from structural damage more effectively than conventional disease modifying antirheumatic drugs (DMARDs).1–3 However, residual disease activity remains a considerable problem and remissions are seen in <30% of patients with established disease.4

To date, head-to-head comparisons among anti-TNF{alpha} agents do not exist, in part because of the large sample size required to demonstrate either differences between, or equivalence of, treatments. In the absence of head-to-head randomised comparisons of anti-TNF{alpha} agents, claims that one drug is better than the others have been met with scepticism by practising physicians. They generally view these drugs as . . . [Full text of this article]


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This article has been cited by other articles:

  • Hanauer, S. B (2007). Risks and benefits of combining immunosuppressives and biological agents in inflammatory bowel disease: is the synergy worth the risk?. Gut 56: 1181-1183 [Full Text]  

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