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Tenofovir Alafenamide vs. Tenofovir Disoproxil Fumarate in Lowering the Risk of HCC Development in Patients With CHB
Seong Hee Kang1, Hyung Joon Yim1, Seul Ki Han2
1Department of Internal Medicine, Korea University College of Medicine, Seoul, Republic of Korea.
Insights
Tenofovir alafenamide (TAF) significantly reduced hepatocellular carcinoma (HCC) risk compared to tenofovir disoproxil fumarate (TDF) in chronic hepatitis B (CHB) patients. This antiviral therapy comparison highlights TAF as a potentially safer option for preventing liver cancer.
Area of Science:
- Hepatology
- Virology
- Oncology
Background:
- Chronic hepatitis B (CHB) is a global health concern.
- Tenofovir alafenamide (TAF) and tenofovir disoproxil fumarate (TDF) are first-line antiviral treatments for CHB.
- Understanding their comparative risks for hepatocellular carcinoma (HCC) is crucial.
Purpose of the Study:
- To compare the association of TAF versus TDF with the occurrence of HCC in treatment-naive CHB patients.
- To evaluate the long-term safety and efficacy of these antiviral agents regarding HCC development.
Main Methods:
- A multicenter cohort of 1364 treatment-naive CHB patients initiating TAF or TDF was analyzed.
- Propensity score matching and inverse probability of treatment weighting were used to control for confounding factors.
- HCC occurrence was monitored over a median follow-up period of 60 months.
Main Results:
- In the propensity score-matched cohort (n=966), TAF use was associated with a significantly lower risk of HCC compared to TDF.
- Crude incidence rates and 5-year cumulative risks for HCC were lower in the TAF group.
- Multivariable and IPTW analyses consistently showed TAF was protective against HCC (aHR ~0.30).
Conclusions:
- TAF use was associated with a substantial reduction in HCC hazard (approximately 71%) compared to TDF.
- These findings suggest TAF may be a safer alternative for CHB management concerning HCC prevention.
- Further research with larger cohorts and longer follow-up is recommended.
Background:
Tenofovir alafenamide (TAF) and tenofovir disoproxil fumarate (TDF) are guideline-endorsed first-line options for antiviral-naive chronic hepatitis B (CHB). We compared their associations with hepatocellular carcinoma (HCC) occurrence.
Methods:
We assembled a multicenter cohort of 1364 treatment-naive CHB patients initiating either TAF (n = 322) or TDF (n = 1042) between 2012 and 2019. Confounding was addressed using 1:2 propensity score (PS) matching and inverse probability of treatment weighting (IPTW).
Results:
The PS-matched analytic set comprised 966 patients (TAF 322; TDF 644). Over 60 months, nine HCC events occurred (two TAF and seven TDF events). Crude incidence rates were 0.17 and 0.27 per 100 person-years for TAF and TDF, respectively. Five-year cumulative risks were 0.6% (TAF) versus 1.0% (TDF). In multivariable models, TAF remained protective (adjusted hazard ratio [aHR]: 0.29, 95% confidence interval [CI]: 0.13-0.66; p < 0.01). Findings were directionally consistent across subgroups, with the strongest associations observed among patients without diabetes, those who were hepatitis B e antigen-positive, and those with baseline HBV DNA in the 5-8 log10 IU/mL range. In IPTW analyses, TAF was likewise associated with lower HCC risk (aHR: 0.31, 95% CI: 0.14-0.68; p < 0.01).
Conclusions:
Compared with TDF, TAF use was associated with an approximately 71% reduction in HCC hazard. Larger cohorts with longer follow-up are warranted to corroborate these observations.
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