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External validation of models to predict hepatocellular carcinoma in Hepatitis C Virus cured F3-F4 patients

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External validation of models to predict hepatocellular carcinoma in Hepatitis C Virus cured F3-F4 patients

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dc.contributor.author Carvalho-Gomes, Ângela es_ES
dc.contributor.author Valcheva, Tsveta Vladi es_ES
dc.contributor.author Sahuco, Ivan es_ES
dc.contributor.author Vidal, Enrique es_ES
dc.contributor.author Martínez-Arenas, Laura es_ES
dc.contributor.author Vinaixa, Carmen es_ES
dc.contributor.author Aguilera, Victoria es_ES
dc.contributor.author García García, Sonia es_ES
dc.contributor.author Berenguer, Marina es_ES
dc.date.accessioned 2024-10-03T18:25:18Z
dc.date.available 2024-10-03T18:25:18Z
dc.date.issued 2024-05 es_ES
dc.identifier.issn 2050-6406 es_ES
dc.identifier.uri http://hdl.handle.net/10251/209255
dc.description.abstract [EN] Background & AimsSeveral hepatocellular carcinoma (HCC) risk-models have been developed to individualise patient surveillance following sustained viral response (SVR) in Hepatitis C Virus patients. Validation of these models in different cohorts is an important step to incorporate a more personalised risk assessment in clinical practice. We aimed at applying these models to stratify the risk in our patients and potentially determine cost-saving associated with individualised HCC risk-stratification screening strategy. MethodsPatients with baseline F3-4 fibrosis treated with new oral direct-acting antivirals who had reached a SVR were regularly followed as part of the HCC surveillance strategy. Six models were applied: Pons, aMAP, Ioannou, HCC risk, Alonso and Semmler. Validation of the models was performed based on sensitivity and the proportion of patients labelled as "high risk". ResultsAfter excluding 557 with less than 3 fibrosis, 12 without SVR, 18 with a follow up (FU) <1 year, 17 transplant recipients, 16 lost to FU and 31 with HCC at time of antiviral therapy, our cohort consisted of 349 F3-4 SVR patients. Twenty-three patients (6.6%) developed HCC after a median FU of 5.12 years. The sensitivity of the different models varied between 0.17 (Semmler7noalcohol) and 1 (Alonso A and aMAP). The lowest proportion of high-risk patients corresponded to the Semmler-noalcohol model (5%). Sixty-three and 90% of the Alonso A and aMAP patients, respectively were labelled as high risk. The most reliable HCC risk-model applied to our cohort to predict HCC development is the Alonso model (based on fibrosis stage assessed by liver stiffness measurements or Fibrosis-4 index (FIB-4) at baseline and after 1 year, and albumin levels at 1 year) with a-100% sensitivity in detecting HCC among those at high risk and 63% labelled as high risk. The application of the model would have saved the cost of 1290 ultrasound no longer being performed in the 37% low-risk group. ConclusionIn our cohort, the Alonso A model allows the most reliable reduction in HCC screening resulting in safely stopping life-long monitoring in about a third of F3-F4 patients achieving SVR with DAAs.; image es_ES
dc.description.sponsorship Instituto de Salud Carlos III, Grant/Award Numbers: FI20/00033, INT20/00061, PI19/01360; Centro de Investigacion Biomedica en Red de Enfermedades Hepaticas y Digestivas; Gilead Research Scholars, Grant/Award Number: GLD18-192 es_ES
dc.language Inglés es_ES
dc.publisher Sage Publications es_ES
dc.relation.ispartof United European Gastroenterology Journal es_ES
dc.rights Reconocimiento - No comercial - Sin obra derivada (by-nc-nd) es_ES
dc.subject HCC-models es_ES
dc.subject Hepatitis C Virus es_ES
dc.subject Hepatocellular carcinoma es_ES
dc.subject Patient monitoring es_ES
dc.subject Sustained viral response es_ES
dc.title External validation of models to predict hepatocellular carcinoma in Hepatitis C Virus cured F3-F4 patients es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.1002/ueg2.12571 es_ES
dc.relation.projectID info:eu-repo/grantAgreement/ISCIII//FI20%2F00033/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/ISCIII//INT20%2F00061/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/ISCIII//PI19%2F01360/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/Gilead Sciences//GLD18-192/ es_ES
dc.rights.accessRights Abierto es_ES
dc.description.bibliographicCitation Carvalho-Gomes, Â.; Valcheva, TV.; Sahuco, I.; Vidal, E.; Martínez-Arenas, L.; Vinaixa, C.; Aguilera, V.... (2024). External validation of models to predict hepatocellular carcinoma in Hepatitis C Virus cured F3-F4 patients. United European Gastroenterology Journal. https://doi.org/10.1002/ueg2.12571 es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion https://doi.org/10.1002/ueg2.12571 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.identifier.pmid 38720450 es_ES
dc.relation.pasarela S\526223 es_ES
dc.contributor.funder Gilead Sciences es_ES
dc.contributor.funder Instituto de Salud Carlos III es_ES


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