Two-year abatacept retention rate in clinical practice in the French ACTION cohort - 06/09/19
Cet article a été publié dans un numéro de la revue, cliquez ici pour y accéder
Abstract |
Objectives |
Abatacept retention rates were evaluated in the French cohort in the prospective ACTION study (2010–2013), which included patients with moderate-to-severe rheumatoid arthritis managed in everyday clinical practice and started on intravenous abatacept therapy.
Methods |
Two-year abatacept retention rates were evaluated in 455 patients classified according to treatment line, body mass index (BMI), and status for rheumatoid factor (RF) and anti-citrullinated peptide antibody (ACPA).
Results |
After 2 years, the overall abatacept retention rate was 44%. The retention rate was non-significantly higher in the patients with vs. without a history of unresponsiveness to at least one biologic (48.1% vs. 41.8%, respectively). No significant retention rate differences were found across BMI categories (444 patients; <25, 45.5%; ≥25 to <30, 48.9%; and ≥30, 36.6%). Neither were any significant differences demonstrated according to RF and ACPA status (RF+ and ACPA+, 45.7%; RF+ or ACPA+, 43.8%; and FR− and ACPA−, 39.1%).
Conclusion |
The 44% 2-year retention rate in the French ACTION cohort supports the usefulness of abatacept therapy. In this study, retention was not associated with treatment line, BMI, or antibody status.
Le texte complet de cet article est disponible en PDF.Keywords : Abatacept, Biologic, Real-life study, Drug retention rate, Rheumatoid arthritis, National specificity
Plan
Bienvenue sur EM-consulte, la référence des professionnels de santé.
L’accès au texte intégral de cet article nécessite un abonnement.
Déjà abonné à cette revue ?