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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorCéspedes-Martínez, Elena
dc.contributor.authorSerra-Ruiz, Xavier
dc.contributor.authorLarrosa, María Nieves
dc.contributor.authorrobles, virginia
dc.contributor.authorHerrera-deGuise, Claudia
dc.contributor.authorMayorga Ayala, Luis Fernando
dc.contributor.authorGarcía García, Sonia
dc.contributor.authorCasellas, Francesc
dc.contributor.authorBORRUEL, NATALIA
dc.date.accessioned2025-10-06T07:25:36Z
dc.date.available2025-10-06T07:25:36Z
dc.date.issued2025-07
dc.identifier.citationCéspedes-Martínez E, Robles-Alonso V, Serra-Ruiz X, Herrera-De Guise C, Mayorga-Ayala L, García-García S, et al. Dashboard-Guided Anti-TNF Induction: An Effective Strategy to Minimize Immunogenicity While Avoiding Immunomodulators—A Single-Center Cohort Study. Crohn’s Colitis 360. 2025 Jul;7(3):otaf023.
dc.identifier.issn2631-827X
dc.identifier.urihttp://hdl.handle.net/11351/13778
dc.descriptionImmunogenicity; Pharmacokinetics; Tumor necrosis factor inhibitors
dc.description.abstractBackground: Proactive therapeutic drug monitoring facilitates early dose optimization to prevent primary and secondary failure to antitumor necrosis factor (TNF). We aimed to investigate the impact of dashboard-guided induction dosing strategy on anti-TNF durability and immunogenicity. Methods: We conducted a single-center cohort analysis of patients with Crohn's disease (CD) and Ulcerative colitis (UC) who initiated treatment with infliximab or adalimumab between January 2020 and March 2023. Induction was prospectively personalized using a pharmacokinetic model-guided dosing strategy, with drug measurements at week 2, 6, and 14, and the first dose adjustment occurred in week 4. Data were recorded retrospectively. We assessed treatment durability, pharmacokinetic outcomes, clinical remission (CR), and endoscopic remission (ER), at both weeks 24 and 56. Multivariate analysis and Kaplan-Meier curves were used to compare outcomes. Results: We enrolled 147 patients (92 CD /55 UC). Anti-TNF drug survival probability was 85.00% after a year. Seventy-seven percent of patients were prescribed an intensified dose in the first year, which was associated with improved drug durability. Only 1 patient out of 147 developed antibodies to adalimumab, none to infliximab. After 24 and 52 weeks of treatment 92.5% (136/147) and 72.78% (107/147) of patients achieved CR, respectively. ER was observed in 59.39% (79/133) of patients. The use of immunomodulators or carriage of HLA DQA1*05 variant was not associated with adverse treatment or pharmacokinetic outcomes. Conclusions: Optimizing anti-TNF induction with a dashboard-guide dosing strategy proves to be a valuable approach to enhance treatment durability and clinical outcomes in inflammatory bowel disease patients. Immunogenicity appears to be mitigated by the model, which even mitigates the impact of immunomodulators and overcomes HLA DQA1*05 effect.
dc.language.isoeng
dc.publisherOxford University Press
dc.relation.ispartofseriesCrohn's & Colitis 360;7(3)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectMedicaments - Monitoratge
dc.subjectPosologia
dc.subjectCrohn, Malaltia de - Tractament
dc.subjectFactor de necrosi tumoral - Inhibidors - Ús terapèutic
dc.subject.meshDrug Monitoring
dc.subject.meshTumor Necrosis Factor-alpha
dc.subject.mesh/antagonists & inhibitors
dc.subject.meshCrohn Disease
dc.subject.mesh/drug therapy
dc.titleDashboard-Guided Anti-TNF Induction: An Effective Strategy to Minimize Immunogenicity While Avoiding Immunomodulators—A Single-Center Cohort Study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1093/crocol/otaf023
dc.subject.decsmonitorización de medicamentos
dc.subject.decsfactor de necrosis tumoral alfa
dc.subject.decs/antagonistas & inhibidores
dc.subject.decsenfermedad de Crohn
dc.subject.decs/farmacoterapia
dc.relation.publishversionhttps://doi.org/10.1093/crocol/otaf023
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Céspedes-Martínez E, Robles-Alonso V, Serra-Ruiz X, Herrera-De Guise C, Mayorga-Ayala L, Casellas F] Unitat d’Atenció Crohn Colitis, Servei d’Aparell Digestiu, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [García-García S, Larrosa-García M] Servei de Farmàcia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Borruel N] Unitat d’Atenció Crohn Colitis, Servei d’Aparell Digestiu, Vall d’Hebron Hospital Universitari, Barcelona, Spain. CIBER-EHD, Barcelona, Spain
dc.identifier.pmid40667463
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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