Risk Prediction of Hepatocellular Carcinoma in Patients With Cirrhosis: The ADRESS-HCC Risk Model

被引:127
作者
Flemming, Jennifer A. [1 ]
Yang, Ju Dong [2 ]
Vittinghoff, Eric [3 ]
Kim, W. Ray [4 ]
Terrault, Norah A. [5 ]
机构
[1] Queens Univ, Dept Med, Div Canc Care & Epidemiol, Kingston, ON K7L 3N6, Canada
[2] Univ Arkansas Med Sci, Dept Internal Med, Little Rock, AR 72205 USA
[3] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[4] Stanford Univ, Div Gastroenterol & Hepatol, Stanford, CA 94305 USA
[5] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
hepatocellular carcinoma; cirrhosis; risk model; risk factors; liver cancer; Scientific Registry of Transplant Recipients (SRTR); CHRONIC HEPATITIS-B; UNITED-STATES; CRYPTOGENIC CIRRHOSIS; MANAGEMENT; DISEASE; SCORE;
D O I
10.1002/cncr.28832
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. (c) 2014 American Cancer Society.
引用
收藏
页码:3485 / 3493
页数:9
相关论文
共 30 条
[1]   Hepatocellular Carcinoma Incidence, Mortality, and Survival Trends in the United States From 1975 to 2005 [J].
Altekruse, Sean F. ;
McGlynn, Katherine A. ;
Reichman, Marsha E. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (09) :1485-1491
[2]  
Altman DG, 2000, STAT MED, V19, P453, DOI 10.1002/(SICI)1097-0258(20000229)19:4<453::AID-SIM350>3.3.CO
[3]  
2-X
[4]  
American Cancer Society, 2012, Cancer Facts and Figures 2012
[5]  
[Anonymous], 2012, J HEPATOL, V56, P908
[6]   Management of Hepatocellular Carcinoma: An Update [J].
Bruix, Jordi ;
Sherman, Morris .
HEPATOLOGY, 2011, 53 (03) :1020-1022
[7]   Cryptogenic cirrhosis: Clinical characterization and risk factors for underlying disease [J].
Caldwell, SH ;
Oelsner, DH ;
Iezzoni, JC ;
Hespenheide, EE ;
Battle, EH ;
Driscoll, CJ .
HEPATOLOGY, 1999, 29 (03) :664-669
[8]  
Centers for Disease Control and Prevention/National Center for Health Statistics, MORT FIL
[9]   Utilization of Surveillance for Hepatocellular Carcinoma Among Hepatitis C Virus-Infected Veterans in the United States [J].
Davila, Jessica A. ;
Henderson, Louise ;
Kramer, Jennifer R. ;
Kanwal, Fasiha ;
Richardson, Peter A. ;
Duan, Zhigang ;
El-Serag, Hashem B. .
ANNALS OF INTERNAL MEDICINE, 2011, 154 (02) :85-+
[10]   Prolonged Therapy of Advanced Chronic Hepatitis C with Low-Dose Peginterferon [J].
Di Bisceglie, Adrian M. ;
Shiffman, Mitchell L. ;
Everson, Gregory T. ;
Lindsay, Karen L. ;
Everhart, James E. ;
Wright, Elizabeth C. ;
Lee, William M. ;
Lok, Anna S. ;
Bonkovsky, Herbert L. ;
Morgan, Timothy R. ;
Ghany, Marc G. ;
Morishima, Chihiro ;
Snow, Kristin K. ;
Dienstag, Jules L. .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 359 (23) :2429-2441