GES: A validated simple score to predict the risk of HCC in patients with HCV-GT4-associated advanced liver fibrosis after oral antivirals

被引:40
作者
Shiha, Gamal [1 ,2 ]
Waked, Imam [3 ]
Soliman, Reham [1 ,4 ]
Elbasiony, Mohamed [1 ,2 ]
Gomaa, Asmaa [3 ]
Mikhail, Nabiel N. H. [1 ,5 ]
Eslam, Mohammed [6 ,7 ]
机构
[1] Egyptian Liver Res Inst & Hosp ELRIAH, Mansoura, Egypt
[2] Mansoura Univ, Fac Med, Internal Med Dept, Hepatol & Gastroenterol Unit, Mansoura, Egypt
[3] Menoufia Univ, Natl Liver Inst, Hepatol Dept, Shibin Al Kawm, Egypt
[4] Port Said Univ, Fac Med, Trop Med Dept, Port Said, Egypt
[5] Assiut Univ, South Egypt Canc Inst, Biostat & Canc Epidemiol Dept, Asyut, Egypt
[6] Westmead Hosp, Storr Liver Ctr, Westmead Inst Med Res, Sydney, NSW, Australia
[7] Univ Sydney, Sydney, NSW, Australia
关键词
CHC; DAAs; HCC risk score; HEPATITIS-C PATIENTS; HEPATOCELLULAR-CARCINOMA;
D O I
10.1111/liv.14666
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims Hepatocellular carcinoma (HCC) risk persists after hepatitis C virus (HCV) eradication with direct-acting antivirals (DAAs), particularly in patients with cirrhosis. Identifying those who are likely to develop HCC is a critical unmet medical need. Our aim is to develop a score that offers individualized patient HCC risk prediction. Methods This two-centre prospective study included 4400 patients, with cirrhosis and advanced fibrosis who achieved a sustained virologic response (SVR), including 2372 patients (derivation cohort). HCC-associated factors were identified by multivariable Cox regression analysis to develop a scoring model for prediction of HCC risk; and subsequently internally and externally validated in two independent cohorts of 687 and 1341 patients. Results In the derivation cohort, the median follow-up was 23.51 +/- 8.21 months, during which 109 patients (4.7%) developed HCC. Age, sex, serum albumin, alpha fetoprotein and pretreatment fibrosis stage were identified as risk factors for HCC. A simple predictive model (GES) score was constructed. The 2-year cumulative HCC incidence using Kaplan-Meier method was 1.2%, 3.3% and 7.1% in the low-risk, medium-risk and high-risk groups respectively. Internal and external validation showed highly significant difference among the three risk groups (P < .001) with regard to cumulative HCC risk. GES score has high predictive ability value (Harrell's C statistic 0.801), that remained robustly consistent across two independent validation cohorts (Harrell's C statistic 0.812 and 0.816). Conclusion GES score is simple with validated good predictive ability for the development of HCC after eradication of HCV and may be useful for HCC risk stratification in those patients.
引用
收藏
页码:2828 / 2833
页数:6
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