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

被引:0
作者
Carvalho-Gomes, Angela [1 ,2 ,8 ]
Valcheva, Tsveta Vladi Valcheva [1 ,3 ]
Sahuco, Ivan [1 ]
Vidal, Enrique [4 ,5 ]
Martinez-Arenas, Laura [1 ,2 ,6 ]
Vinaixa, Carmen [1 ,2 ,7 ]
Aguilera, Victoria [1 ,2 ,7 ]
Garcia, Sonia Garcia [7 ]
Berenguer, Marina [1 ,2 ,3 ,7 ,8 ]
机构
[1] Le Fe Hlth Res Inst IIS Le Fe, Hepatol Hepatobiliopancreat Surg & Transplant Grp, Valencia, Spain
[2] Inst Salud Carlos III ISCIII, Natl Inst Study Liver & Gastrointestinal Dis, CIBEREHD, Madrid, Spain
[3] Univ Valencia, Med Dept, Valencia, Spain
[4] Hlth Res Inst Hosp La Fe, Lab Cellular & Mol Biol, Valencia, Spain
[5] Hlth Res Inst Hosp La Fe, Clin & Translat Res Canc, Valencia, Spain
[6] Univ Politecn Valencia, Dept Biotechnol, Valencia, Spain
[7] La Fe Univ Hosp, Dept Gastroenterol, Hepatol Unit, Valencia, Spain
[8] Le Fe Univ Hosp, IIS Le Fe, Hepatol HBP Surg & Transplant CIBEREHD Unit, Avda Fernando Abril Martorell 106,Planta 5,Lab 5-2, Valencia 46026, Spain
关键词
HCC-models; Hepatitis C Virus; hepatocellular carcinoma; patient monitoring; sustained viral response; SUSTAINED VIROLOGICAL RESPONSE; RISK; THERAPY;
D O I
10.1002/ueg2.12571
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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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页码:901 / 910
页数:10
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