Swiss consensus statement: Recommendations for optimising re-treatment with MabThera (rituximab) in rheumatoid arthritis.

Détails

Ressource 1Télécharger: 20648402.pdf (283.19 [Ko])
Etat: Public
Version: Final published version
ID Serval
serval:BIB_779E45263C43
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Synthèse (review): revue aussi complète que possible des connaissances sur un sujet, rédigée à partir de l'analyse exhaustive des travaux publiés.
Collection
Publications
Institution
Titre
Swiss consensus statement: Recommendations for optimising re-treatment with MabThera (rituximab) in rheumatoid arthritis.
Périodique
Swiss medical weekly
Auteur⸱e⸱s
Dudler J., Finckh A., Kyburz D., Langenegger T., Möller B., Schmiedel U., Walker U.A.
ISSN
1424-3997 (Electronic)
ISSN-L
0036-7672
Statut éditorial
Publié
Date de publication
16/07/2010
Peer-reviewed
Oui
Volume
140
Pages
w13073
Langue
anglais
Notes
Publication types: Consensus Development Conference ; Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: epublish
Résumé
Rituximab is an effective treatment of rheumatoid arthritis (RA), which has been approved for the treatment of moderate to severe disease in patients with an inadequate response to anti-TNF therapies. Rituximab differs from other available biological agents for RA by way of its unique mode of action and unrivalled long dosing interval. The efficacy of rituximab subsides progressively over time and re-therapy is generally required to maintain long term disease control. The timing of re-treatment is currently not well established and varies widely in clinical practice. The present document is a concise recommendation regarding re-treatment with rituximab, based on validated outcomes such as the DAS28 and the EULAR response criteria. The recommendation was established through consensus between practitioners familiar with rituximab therapy in RA. Optimisation of the rituximab re-treatment schedule may improve patient outcomes and balance risks and benefits for the individual patient.

Mots-clé
Antibodies, Monoclonal, Murine-Derived/adverse effects, Antibodies, Monoclonal, Murine-Derived/therapeutic use, Antirheumatic Agents/adverse effects, Antirheumatic Agents/therapeutic use, Arthritis, Rheumatoid/drug therapy, Arthritis, Rheumatoid/psychology, Dose-Response Relationship, Drug, Drug Administration Schedule, Evidence-Based Medicine/standards, Follow-Up Studies, Humans, Quality of Life/psychology, Retreatment, Risk Assessment, Rituximab, Switzerland, Treatment Outcome
Pubmed
Web of science
Open Access
Oui
Création de la notice
04/11/2010 10:58
Dernière modification de la notice
20/08/2019 15:34
Données d'usage