Subcutaneous infliximab cut-off points in patients with inflammatory bowel disease. Data from the ENEIDA registry.

Inflammatory Bowel Disease Infliximab through levels Subcutaneous

Journal

Journal of Crohn's & colitis
ISSN: 1876-4479
Titre abrégé: J Crohns Colitis
Pays: England
ID NLM: 101318676

Informations de publication

Date de publication:
22 Aug 2024
Historique:
received: 14 05 2024
medline: 22 8 2024
pubmed: 22 8 2024
entrez: 22 8 2024
Statut: aheadofprint

Résumé

Switching from the intravenous to the subcutaneous biosimilar infliximab (SC-IFX) has been shown to safely maintain clinical remission and increase drug levels in patients with Crohn's disease (CD) and ulcerative colitis (UC). The aim of this study was to evaluate long-term outcomes after switching from intravenous IFX (IV-IFX) to SC-IFX, the drug concentration thresholds for maintaining remission and other predictors for loss of response after the switch. Multicenter observational study involving CD and UC patients who were in clinical remission for at least 24 weeks and scheduled to switch from IV-IFX to SC-IFX. Two hundred and twenty patients were included [74 UC (34%) and 146 (66%) CD]. IV-IFX was administered for 52.5 months [range 25-89]. Pre-switch, 106 (49%) patients were receiving intensified IV-IFX. While SC-IFX levels significantly increased following the switch from IV to SC-IFX, clinical parameters, C-reactive protein and faecal calprotectin remained unchanged during follow-up. SC-IFX levels were significantly higher between patients receiving the standard IV-IFX dose than those with the intensified dose. Immunomodulator therapy at baseline and perianal disease had no effect on IFX trough levels, whereas higher body mass index was associated with increased levels. The suggested optimal SC-IFX cut-off concentration for clinical and biochemical remission based on ROC analysis was 12.2 μg/mL (AUC: 0.62) at week 12 and 13.2 μg/mL (AUC: 0.57) at week 52. Drug persistence was 92% at week 52, with a good safety profile. Switching from IV-IFX to SC-IFX safely maintains long-term remission in patients with CD and UC. In maintenance, the optimal cut-off point associated with remission was 12-13 μg/mL.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Switching from the intravenous to the subcutaneous biosimilar infliximab (SC-IFX) has been shown to safely maintain clinical remission and increase drug levels in patients with Crohn's disease (CD) and ulcerative colitis (UC). The aim of this study was to evaluate long-term outcomes after switching from intravenous IFX (IV-IFX) to SC-IFX, the drug concentration thresholds for maintaining remission and other predictors for loss of response after the switch.
METHODS METHODS
Multicenter observational study involving CD and UC patients who were in clinical remission for at least 24 weeks and scheduled to switch from IV-IFX to SC-IFX.
RESULTS RESULTS
Two hundred and twenty patients were included [74 UC (34%) and 146 (66%) CD]. IV-IFX was administered for 52.5 months [range 25-89]. Pre-switch, 106 (49%) patients were receiving intensified IV-IFX. While SC-IFX levels significantly increased following the switch from IV to SC-IFX, clinical parameters, C-reactive protein and faecal calprotectin remained unchanged during follow-up. SC-IFX levels were significantly higher between patients receiving the standard IV-IFX dose than those with the intensified dose. Immunomodulator therapy at baseline and perianal disease had no effect on IFX trough levels, whereas higher body mass index was associated with increased levels. The suggested optimal SC-IFX cut-off concentration for clinical and biochemical remission based on ROC analysis was 12.2 μg/mL (AUC: 0.62) at week 12 and 13.2 μg/mL (AUC: 0.57) at week 52. Drug persistence was 92% at week 52, with a good safety profile.
CONCLUSION CONCLUSIONS
Switching from IV-IFX to SC-IFX safely maintains long-term remission in patients with CD and UC. In maintenance, the optimal cut-off point associated with remission was 12-13 μg/mL.

Identifiants

pubmed: 39171615
pii: 7738597
doi: 10.1093/ecco-jcc/jjae127
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of European Crohn’s and Colitis Organisation. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Auteurs

Marisa Iborra (M)

Gastroenterology. Hospital Universitario y Politécnico La Fe. Valencia, España.

Berta Caballol (B)

Unidad de enfermedad inflamatoria intestinal. Hospital Clínic Barcelona.IDIBAPS. CIBER-EHD. Barcelona, España.

Alejandro Garrido (A)

Gastroenterology. Hospital Universitario y Politécnico La Fe. Valencia, España.

José María Huguet (JM)

Gastroenterology. Hospital General Universitario de Valencia. Valencia, España.

Francisco Mesonero (F)

Gastroenterology. Hospital Universitario Ramón y Cajal. Madrid, España.

Ángel Ponferrada (Á)

Gastroenterology. Hospital Universitario Infanta Leonor. Madrid, España.

Lara Arias García (L)

Gastroenterology. Hospital Universitario de Burgos. Burgos, España.

Marta Maia Boscá Watts (MM)

Gastroenterology. Hospital Clínico Universitario de Valencia. Valencia, España.

Samuel J Fernández Prada (SJ)

Gastroenterology. Hospital Rio Hortega. Valladolid, España.

Eduard Brunet Mas (E)

Gastroenterology. Hospital Universitari Parc Taulí. Institut d'Investigació i Innovació Parc Taulí I3PT-CERCA and Departament de Medicina- Universitat Autònoma de Barcelona CIBERehd-Instituto de Salud Carlos III. Sabadell, España.

Ana Gutiérrez Casbas (A)

Gastroenterology. Hospital General Universitario Dr. Balmis de Alicante. Alicante, España. ISABIAL. CIBERehd.

Elena Cerrillo (E)

Gastroenterology. Hospital Universitario y Politécnico La Fe. Valencia, España.

Ingrid Ordás (I)

Unidad de enfermedad inflamatoria intestinal. Hospital Clínic Barcelona.IDIBAPS. CIBER-EHD. Barcelona, España.

Lucía Ruiz (L)

Gastroenterology. Hospital General Universitario de Valencia. Valencia, España.

Irene García de la Filia (I)

Gastroenterology. Hospital Universitario Ramón y Cajal. Madrid, España.

Jaime Escobar Ortiz (J)

Gastroenterology. Hospital Universitario Infanta Leonor. Madrid, España.

Beatriz Sicilia (B)

Gastroenterology. Hospital Universitario de Burgos. Burgos, España.

Elena Ricart (E)

Unidad de enfermedad inflamatoria intestinal. Hospital Clínic Barcelona.IDIBAPS. CIBER-EHD. Barcelona, España.

Eugeni Domènech (E)

Gastroenterology. Hospital Universitari Germans Trias i Pujol, Badalona, Departament de Medicina- Universitat Autònoma de Barcelona, CIBER-EHD.

Pilar Nos (P)

Gastroenterology. Hospital Universitario y Politécnico La Fe. Valencia, España.

Classifications MeSH