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. 2014 Nov 15;120(22):3485-93.
doi: 10.1002/cncr.28832. Epub 2014 Jul 16.

Risk prediction of hepatocellular carcinoma in patients with cirrhosis: the ADRESS-HCC risk model

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Risk prediction of hepatocellular carcinoma in patients with cirrhosis: the ADRESS-HCC risk model

Jennifer A Flemming et al. Cancer. .

Abstract

Background: All patients with cirrhosis are at risk of developing hepatocellular carcinoma (HCC). This risk is not uniform because other patient-related factors influence the risk of HCC. The objective of the current study was to develop an HCC risk prediction model to estimate the 1-year probability of HCC to assist with patient counseling.

Methods: Between 2002 and 2011, a cohort of 34,932 patients with cirrhosis was identified from a national liver transplantation waitlist database from the United States. Cox proportional hazards regression methods were used to develop and validate a risk prediction model for incident HCC. In the validation cohort, discrimination and calibration of the model was examined. External validation was conducted using patients with cirrhosis who were enrolled in the Hepatitis C Antiviral Long-term Treatment against Cirrhosis (HALT-C) study.

Results: HCC developed in 1960 patients (5.6%) during a median follow-up of 1.3 years (interquartile range, 0.47 years-2.83 years). Six baseline clinical variables, including age, diabetes, race, etiology of cirrhosis, sex, and severity (ADRESS) of liver dysfunction were independently associated with HCC and were used to develop the ADRESS-HCC risk model. C-indices in the derivation and internal validation cohorts were 0.704 and 0.691, respectively. In the validation cohort, the predicted cumulative incidence of HCC by the ADRESS-HCC model closely matched the observed data. In patients with cirrhosis in the HALT-C cohort, the model stratified patients correctly according to the risk of developing HCC within 5 years.

Conclusions: The ADRESS-HCC risk model is a useful tool for predicting the 1-year risk of HCC among patients with cirrhosis.

Keywords: Scientific Registry of Transplant Recipients (SRTR); cirrhosis; hepatocellular carcinoma; liver cancer; risk factors; risk model.

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Figures

Figure 1
Figure 1
Development of the derivation and validation cohorts from the Scientific Registry of Transplant Recipients database is shown. HCC indicates hepatocellular carcinoma.
Figure 2
Figure 2
Calibration of the ADRESS (age, diabetes, race, etiology of cirrhosis, sex, and severity)- a) Calibration plot in the internal validation cohort (n=17,808) and b) receiver operating curve of the entire cohort (n=34,932).
Figure 3
Figure 3
ADRESS (age, diabetes, race, etiology of cirrhosis, sex, and severity)- hepatocellular carcinoma (HCC) risk model score and probability of HCC in the HALT-C (Hepatitis C Antiviral Long-term Treatment against Cirrhosis) cohort is shown. Low indicates first quartile, intermediate, second and third quartiles; high, fourth quartile (P <.01, log-rank test).

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