Anti-TNF dose escalation and drug sustainability in Crohn's disease : Data from the nationwide administrative database in Hungary

Kósa, Fruzsina; Kunovszki, Péter; Borsi, András; Iliás, Ákos [Iliás, Ákos (gasztroenterológia), szerző] I. Sz. Belgyógyászati Klinika (SE / AOK / K); Palatka, Károly; Szamosi, Tamás [Szamosi, Tamás (Gasztroenterológia), szerző]; Vincze, Áron [Vincze, Áron (Klinikai gasztroe...), szerző] I.sz. Belgyógyászati Klinika (PTE / ÁOK); Molnár, Tamás [Molnár, Tamás (belgyógyászat-gas...), szerző] I. sz. Belgyógyászati Klinika (SZTE / ÁOK); Lakatos, Peter L ✉ [Lakatos, Péter László (Belgyógyászat, ga...), szerző] I. Sz. Belgyógyászati Klinika (SE / AOK / K)

Angol nyelvű Tudományos Szakcikk (Folyóiratcikk)
Megjelent: DIGESTIVE AND LIVER DISEASE 1590-8658 1878-3562 52 (3) pp. 274-280 2020
  • SJR Scopus - Gastroenterology: Q2
Azonosítók
A significant percentage of patients receiving anti-tumor necrosis factor alpha (anti-TNFα) agents lose clinical response over time. This study aims to provide representative real-world data on anti-TNFα drug sustainability, prevalence and predictors of anti-TNFα dose escalation.In this nationwide, retrospective study, patients receiving infliximab or adalimumab therapy between 2013 and 2016 were included using the administrative claims database of the Hungarian National Health Insurance Fund. Demographic characteristics, drug sustainability, dose escalation, use of parallel medications were analyzed.476 infliximab and 397 adalimumab patients were included. Dose escalation was observed in 7%, 9% and 22% of patients receiving originator/biosimilar infliximab and adalimumab during the complete follow-up, respectively. Dose escalation was associated with shorter disease duration (OR = 1.75, p = 0.026) and corticosteroid use. Drug retention rates were 62.7%, 72.3%, 75.4% after 1 year follow-up for Remicade®, Inflectra® and Humira®, which decreased to 38.3% and 52.1% for Remicade® and Humira® at 3 years. Drug sustainability was affected by steroid use prior biologic initiation in adalimumab treated patients (HR = 2.04, p < 0.001), while in infliximab treated patients dose escalation (HR = 0.51, p = 0.02) and gender (HR = 1.39, p = 0.033) were predictors of treatment discontinuation.Dose escalation rates were lower in this real-world administrative database study for both adalimumab and infliximab compared to published data. Drug retention rates were overall satisfactory, with no apparent difference between the legacy and biosimilar infliximab.
Hivatkozás stílusok: IEEEACMAPAChicagoHarvardCSLMásolásNyomtatás
2020-08-03 22:39