Zusammenfassung
Seit 2006 ist Rituximab (RTX) für die Behandlung von Patienten mit rheumatoider Arthritis zugelassen, die auf eine frühere TNF-Blockertherapie nicht angesprochen bzw. diese nicht vertragen haben. In diesen überarbeiteten Therapieempfehlungen werden neue Studiendaten zur Evaluation des therapeutischen Ansprechens, zur Retherapie sowie die Bedeutung von prädiktiven Faktoren für das Ansprechen und Sicherheitsaspekte aktualisiert und diskutiert.
Abstract
Treatment with rituximab (RTX) has been approved since 2006 for patients with rheumatoid arthritis who previously failed to respond to tumor necrosis factor (TNF) inhibitor therapy or who experienced side effects. In these updated treatment recommendations new data relating to evaluation of the therapeutic response, retreatment, the role of predictive factors as well as safety data are incorporated and discussed.
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Einhaltung ethischer Richtlinien
Interessenkonflikt. Die Autoren weisen auf folgende Beziehungen hin: A. Rubbert-Roth: Vorträge bzw. Advisory Boards von folgenden Firmen: Abbott, Amgen, BMS, Chugai, MSD, Pfizer, Roche, UCB. G. R. Burmester: Klinische Studien für AbbVie, BMS, MedImmune, Novartis, Pfizer, Roche, UCB sowie Consulting/Lectures bei AbbVie, BMS, MSD, Novartis, Pfizer, Roche, UCB. A. Gause: Abbvie, BMS, Chugai, MSD, Roche, UCB nur Referententätigkeit und Beratung. T. Dörner: Studienunterstützung von Roche/Chugai, UCB, Sanofi und Honorare für Beratung von Roche/Chugai, UCB, Sanofi. Dieser Beitrag beinhaltet keine Studien an Menschen oder Tieren.
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Rubbert-Roth, A., Burmester, G., Dörner, T. et al. Empfehlungen zum Einsatz von Rituximab bei Patienten mit rheumatoider Arthritis. Z. Rheumatol. 73, 165–174 (2014). https://doi.org/10.1007/s00393-013-1238-2
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DOI: https://doi.org/10.1007/s00393-013-1238-2