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Cited 22 time in webofscience Cited 25 time in scopus
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Validation of the CAMD Score in Patients With Chronic Hepatitis B Virus Infection Receiving Antiviral Therapyopen access

Authors
Kim, Seung UpSeo, Yeon SeokLee, Han AhKim, Mi NaKim, Eun HwaKim, Ha YanLee, Yu RimLee, Hye WonPark, Jun YongKim, Do YoungAhn, Sang HoonHan, Kwang-HyubHwang, Seong GyuRim, Kyu SungUm, Soon HoTak, Won YoungKweon, Young OhKim, Beom KyungPark, Soo Young
Issue Date
Mar-2020
Publisher
ELSEVIER SCIENCE INC
Keywords
Hepatitis B Virus; Hepatocellular Carcinoma; Prediction; Model; CAMD Score; Validation
Citation
Clinical Gastroenterology and Hepatology, v.18, no.3, pp 693 - 699.e1
Indexed
SCIE
SCOPUS
Journal Title
Clinical Gastroenterology and Hepatology
Volume
18
Number
3
Start Page
693
End Page
699.e1
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/957
DOI
10.1016/j.cgh.2019.06.028
ISSN
1542-3565
1542-7714
Abstract
BACKGROUND & AIMS: Researchers previously developed a scoring system to determine the risk of hepatocellular carcinoma (HCC) in patients with chronic hepatitis B virus (HBV) infection, based on the presence of cirrhosis, patient age, male sex, and diabetes (called the CAMD scoring system). We validated the CAMD scoring system and compared its performance with that of other risk assessment models in an independent cohort. METHODS: We followed up 3277 patients with chronic HBV infection (mean age, 48.7 y; 62.6% male; 32.4% with cirrhosis) who were treated with entecavir (n = 1725) or tenofovir (n = 1552) as the first-line antiviral agent in 4 academic teaching hospitals in the Republic of Korea. The primary outcome was development of HCC. We evaluated the ability of the CAMD, PAGE-B, and mPAGE-B scoring systems to identify patients who would develop HCC using integrated area under the curve (iAUC) analysis. RESULTS: Over a median follow-up period of 58.2 months, 8.9% of the patients developed HCC. Patients who developed HCC were older, more likely to be male, and had higher proportions of cirrhosis and diabetes than patients who did not develop HCC (all P < .05). CAMD scores identified patients who developed HCC with an iAUC of 0.790, mPAGE-B scores with an iAUC of 0.769, and PAGE-B scores with an iAUC of 0.760. The 5-year cumulative risks of HCC were 1.3% in patients with low CAMD scores (<8), 8.0% in patients with intermediate CAMD scores (8-13), and 24.3% in patients with high CAMD scores (>13) (P < .001 for comparison of low- vs intermediate-score groups and between intermediate- vs high-score groups). The predicted and observed probabilities of HCC had excellent agreement. CONCLUSIONS: We validated the CAMD scoring system in determining the risk of HCC in patients with chronic HBV treatment receiving entecavir or tenofovir treatment. Validation was performed in a cohort of patients in the Republic of Korea, where most patients have genotype C2 HBV infection.
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Seo, Yeon Seok
Anam Hospital (Department of Gastroenterology and Hepatology, Anam Hospital)
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