한빛사논문
Jiwon Yang 1, Won-Mook Choi1, Ju Hyun Shim1, Danbi Lee1, Kang Mo Kim1, Young-Suk Lim1, Han Chu Lee1, Jonggi Choi1,a
1Department of Gastroenterology, Liver Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
aCorrespondence to: Jonggi Choi, MD, PhD
Abstract
Background and aims: The initiation of antiviral treatment in chronic hepatitis B (CHB) patients with compensated cirrhosis and low-level viremia (LLV; HBV DNA 15-2,000 IU/mL) remains controversial. We sought to compare the long-term outcomes of these untreated patients according to their viremic status.
Methods: 627 CHB untreated patients with compensated cirrhosis were analyzed retrospectively. The risk of hepatocellular carcinoma (HCC) and liver-related clinical events, including hepatic decompensation, were compared between patients with LLV and undetectable HBV DNA. Patients who received antiviral treatment were censored at the time of treatment initiation.
Results: The mean age of the patients was 54.7 years, 64.4 % of whom were male. During the study period, 59 patients developed HCC (20 and 39 in the undetectable and LLV groups, respectively) with an annual incidence of 2.44/100 person-years (PYs). Multivariable analysis revealed that the LLV group was associated with a significantly higher risk of HCC (adjusted hazard ratio [HR]: 2.36, p=0.002) than the undetectable group. In the 204 propensity-score (PS) matched cohort, the LLV group had a 2.16-fold greater risk of HCC than the undetectable group (p=0.014). Liver-related clinical events occurred in 121 patients with an annual incidence of 5.25/100 PYs. Despite not reaching statistical significance, the LLV group tended to have a higher risk of liver-related events in the PS-matched cohort (HR: 1.14, p=0.50).
Conclusion: Compared with patients with undetectable HBV DNA, those with compensated cirrhosis and LLV had a significantly higher risk of HCC. Antiviral treatment should be advised for these patients.
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