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
Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10251/209255
Título:
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External validation of models to predict hepatocellular carcinoma in Hepatitis C Virus cured F3-F4 patients
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Autor:
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Carvalho-Gomes, Ângela
Valcheva, Tsveta Vladi
Sahuco, Ivan
Vidal, Enrique
Martínez-Arenas, Laura
Vinaixa, Carmen
Aguilera, Victoria
García García, Sonia
Berenguer, Marina
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Fecha difusión:
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Resumen:
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[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 ...[+]
[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
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Palabras clave:
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HCC-models
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Hepatitis C Virus
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Hepatocellular carcinoma
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Patient monitoring
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Sustained viral response
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Derechos de uso:
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Reconocimiento - No comercial - Sin obra derivada (by-nc-nd)
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Fuente:
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United European Gastroenterology Journal. (issn:
2050-6406
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DOI:
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10.1002/ueg2.12571
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Editorial:
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Sage Publications
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Versión del editor:
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https://doi.org/10.1002/ueg2.12571
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Código del Proyecto:
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info:eu-repo/grantAgreement/ISCIII//FI20%2F00033/
info:eu-repo/grantAgreement/ISCIII//INT20%2F00061/
info:eu-repo/grantAgreement/ISCIII//PI19%2F01360/
info:eu-repo/grantAgreement/Gilead Sciences//GLD18-192/
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Agradecimientos:
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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[+]
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
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Tipo:
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Artículo
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