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Casanova, María José; Nantes, Óscar; Varela, Pilar; Vela‐González, Milagros; Rivero, Montserrat; Sierra‐Gabarda, Olivia; Riestra, Sabino; Barreiro‐de Acosta, Manuel; Martín‐Rodríguez, María del Mar; Gargallo‐Puyuelo, Carla Jerusalén; Reygosa, Cristina; Muñoz, Roser; Filia‐Molina, Irene García; Núñez‐Ortiz, Andrea; Kolle, Lilyan; Calafat, Margalida; Huguet, José María; Iglesias‐Flores, Eva; Martínez‐Pérez, Teresa de Jesús; Bosch, Orencio; Duque‐Alcorta, José María; Frago‐Larramona, Santiago; Van Domselaar, Manuel; González‐Cosano, Víctor Manuel; Bujanda, Luis; Rubio, Saioa; Mancebo, Alejo; Castro, Beatriz; García‐López, Santiago; Francisco, Ruth; Nieto‐García, Laura; Laredo, Viviana; Gutiérrez‐Casbas, Ana; Mesonero, Francisco; Leo‐Carnerero, Eduardo; Cañete, Fiorella; Ruiz, Lucía; Gros, Beatriz; Moral‐Martínez, María; Rodríguez, Cristina; Chaparro, María; Gisbert, Javier P.
Alimentary pharmacology & therapeutics, July 2023, 2023-Jul, 2023-07-00, 20230701, Letnik: 58, Številka: 1Journal Article
Summary Background and Aims Data on the outcomes after switching from adalimumab (ADA) originator to ADA biosimilar are limited. The aim was to compare the treatment persistence, clinical efficacy, and safety outcomes in inflammatory bowel disease patients who maintained ADA originator vs. those who switched to ADA biosimilar. Methods Patients receiving ADA originator who were in clinical remission at standard dose of ADA originator were included. Patients who maintained ADA originator formed the non‐switch cohort (NSC), and those who switched to different ADA biosimilars constituted the switch cohort (SC). Clinical remission was defined as a Harvey–Bradshaw index ≤4 in Crohn's disease and a partial Mayo score ≤2 in ulcerative colitis. To control possible confounding effects on treatment discontinuation, an inverse probability treatment weighted proportional hazard Cox regression was performed. Results Five hundred and twenty‐four patients were included: 211 in the SC and 313 in the NSC. The median follow‐up was 13 months in the SC and 24 months in the NSC (p < 0.001). The incidence rate of ADA discontinuation was 8% and 7% per patient‐year in the SC and in the NSC, respectively (p > 0.05). In the multivariate analysis, switching from ADA originator to ADA biosimilar was not associated with therapy discontinuation. The incidence rate of relapse was 8% per patient‐year in the SC and 6% per patient‐year in the NSC (p > 0.05). Six percent of the patients had adverse events in the SC vs. 5% in the NSC (p > 0.05). Conclusion Switching to ADA biosimilar did not impair patients' outcomes in comparison with maintaining on the originator.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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in: SICRIS
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