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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 |