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Negligible HCC risk during stringently defined untreated immune-tolerant phase of chronic hepatitis B

Authors
 Lee, Hye Won  ;  Chon, Young Eun  ;  Kim, Beom Kyung  ;  Yip, Terry Cheuk-Fung  ;  Tse, Yee-Kit  ;  Wong, Grace Lai-Hung  ;  Wong, Vincent Wai-Sun  ;  Chan, Henry Lik-Yuen  ;  Ahn, Sang Hoon 
Citation
 European Journal of Internal Medicine, Vol.84 : 68-73, 2021-02 
Journal Title
EUROPEAN JOURNAL OF INTERNAL MEDICINE
ISSN
 0953-6205 
Issue Date
2021-02
Keywords
Hepatitis B virus ; Immune-tolerant ; Antiviral therapy ; Hepatitis B e antigen ; Hepatocellular carcinoma
Abstract
Background & aims: Whether chronic hepatitis B (CHB) patients during immune-tolerant (IT) phase are at low risk of hepatocellular carcinoma (HCC) is still controversial. We performed a multicenter study to determine their long-term prognosis. Methods: Untreated IT group included patients < 40 years of age, with persistently hepatitis B e antigen [HBeAg] positivity, serum HBV-DNA>6 log(10)I U/mL, and ALT level < 40 U/L, using age and HBV-DNA criteria by the American Association for the Study of Liver Diseases (AASLD) guideline. Cumulative HCC risk of untreated IT group (n=194) was compared to HBeAg-positive patients undergoing antiviral therapy according to the practice and reimbursement guidelines (treated HBeAg[+] group, n=454). Patients with history of cirrhosis or HCC at baseline were excluded. Results: During follow-up (median 62.1 months), HCC did not develop in any patient among untreated IT group, whereas the cumulative probability of HCC at 3, 5, and 9 years in the treated HBeAg(+) group was 0.5%, 0.7%, and 1.3%, respectively (p=0.203). Ninety-seven patients among untreated IT group entered immune-active phase, of whom 86 (88.7%) started antiviral treatment. A high normal ALT level (20-39 U/L) was associated with an increased risk of a phase change, compared to ALT < 20 U/L. After censoring at the time of phase change, the cumulative HCC risk was also not significantly different between two groups (p=0.258). Conclusions: No actual HCC risk during untreated IT phase defined by age and HBV-DNA criteria of the AASLD guideline exists, supporting their diagnostic validity from the perspective of long-term prognosis. Further validation studies are required.
DOI
10.1016/j.ejim.2020.10.022
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Beom Kyung(김범경) ORCID logo https://orcid.org/0000-0002-5363-2496
Ahn, Sang Hoon(안상훈) ORCID logo https://orcid.org/0000-0002-3629-4624
Lee, Hye Won(이혜원) ORCID logo https://orcid.org/0000-0002-3552-3560
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/184163
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