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Biological agents in monotherapy for the treatment of rheumatoid arthritis.
Gabay, C; Hasler, P; Kyburz, D; So, A; Villiger, P; von Kempis, J; Walker, U.
Affiliation
  • Gabay C; University Hospitals of Geneva, 26 Avenue Beau-Séjour, 1211, Geneva 14, SWITZERLAND; cem.gabay@hcuge.ch.
Swiss Med Wkly ; 144: w13950, 2014.
Article in En | MEDLINE | ID: mdl-24723273
ABSTRACT
Rheumatoid arthritis (RA) is a chronic, systemic, inflammatory disease, which results in joint destruction and permanent disability. The advent of disease-modifying antirheumatic drugs (DMARDs) has made a profound impact on the outcome and prognosis of RA. Methotrexate (MTX) is a central agent in RA therapy, and is used either alone or in combination with biological DMARDs. However, a large proportion of RA patients (20%-40%) either do not respond to or are unable to tolerate MTX or the alternative agents used in place of MTX (including leflunomide, sulfasalazine, azathioprine, hydroxycholoquine and combination DMARDs). For these patients, monotherapy with biological DMARDs is a key treatment option that balances tolerability with improved clinical outcomes. This article reviews the data for four biological agents approved for use as monotherapy in Switzerland (adalimumab, certolizumab pegol, etanercept and tocilizumab) in order to formulate a consensus statement on their roles in biologic monotherapy of RA.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polyethylene Glycols / Arthritis, Rheumatoid / Immunoglobulin G / Immunoglobulin Fab Fragments / Receptors, Tumor Necrosis Factor / Antirheumatic Agents / Antibodies, Monoclonal, Humanized Type of study: Prognostic_studies Limits: Humans Language: En Journal: Swiss Med Wkly Journal subject: MEDICINA Year: 2014 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polyethylene Glycols / Arthritis, Rheumatoid / Immunoglobulin G / Immunoglobulin Fab Fragments / Receptors, Tumor Necrosis Factor / Antirheumatic Agents / Antibodies, Monoclonal, Humanized Type of study: Prognostic_studies Limits: Humans Language: En Journal: Swiss Med Wkly Journal subject: MEDICINA Year: 2014 Type: Article