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Aspirin Use and Risk of HCC and Gastrointestinal Bleeding in Patients With HBV-Related Cirrhosis: A Landmark Analysis
Mi Na Kim1,2,3, Geun U Park4, Seng Chan You5
1Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.
Insights
Aspirin use in patients with hepatitis B virus (HBV)-related cirrhosis was associated with a reduced risk of hepatocellular carcinoma (HCC). However, aspirin use also significantly increased the risk of gastrointestinal (GI) bleeding in this patient group.
Area of Science:
- Hepatology
- Gastroenterology
- Oncology
Background:
- Hepatitis B virus (HBV)-related cirrhosis poses a significant risk for hepatocellular carcinoma (HCC).
- The role of aspirin in HCC prevention and its associated risks, particularly gastrointestinal (GI) bleeding, remains unclear in HBV-related cirrhosis patients.
Purpose of the Study:
- To investigate the association between aspirin use and the risks of HCC and GI bleeding.
- To evaluate the safety and efficacy of aspirin for HCC prevention in patients with HBV-related cirrhosis.
Main Methods:
- A 3-year landmark analysis was conducted using nationwide cohort data from South Korea's National Health Insurance Service.
- Patients with compensated HBV-related cirrhosis (2005-2017) were included, with aspirin users defined as those prescribed aspirin for ≥90 days.
- Propensity score matching was used to compare the risks of HCC and GI bleeding between aspirin users and nonusers.
Main Results:
- Over a median follow-up of 7.6 years, aspirin users showed a significantly lower 10-year cumulative incidence of HCC (41.8% vs. 46.5%, p=0.033).
- The adjusted hazard ratio (aHR) for HCC was 0.84 (95% CI=0.73-0.96; p=0.013) in the aspirin-treated group.
- Conversely, the 10-year cumulative incidence of GI bleeding was higher in aspirin users (29.5% vs. 24.0%, p=0.016), with an aHR of 1.20 (95% CI=1.02-1.42; p=0.029).
Conclusions:
- Aspirin use in patients with HBV-related cirrhosis is associated with a significantly reduced risk of developing HCC.
- However, aspirin treatment in this population also leads to a significantly increased risk of GI bleeding.
- These findings highlight a critical trade-off between HCC prevention and bleeding risk when considering aspirin for patients with HBV-related cirrhosis.
Background And Aims:
The use of aspirin in hepatocellular carcinoma (HCC) prevention and the risk of gastrointestinal (GI) bleeding is still uncertain in patients with hepatitis B virus (HBV)-related cirrhosis. We investigated the association between aspirin use and the risks of HCC and GI bleeding in patients with HBV-related cirrhosis.
Methods:
We conducted a 3-year landmark analysis using nationwide cohort data from the National Health Insurance Service of South Korea. Patients diagnosed with compensated HBV-related cirrhosis in 2005-2017 were included. Patients who were prescribed aspirin for at least 90 days consecutively during the 3-year exposure period were classified as the aspirin-treated group. The risks of HCC and GI bleeding were estimated in a cohort matched by propensity scores.
Results:
During a median of 7.6 years of follow-up, the 10-year cumulative incidence of HCC was 41.8% among aspirin users (n = 608) and 46.5% among nonusers (n = 2432) (p = 0.033). The aspirin-treated group showed a significantly lower risk of HCC than the untreated group (adjusted hazard ratio [aHR] = 0.84, 95% confidence interval [CI] = 0.73-0.96; p = 0.013). The 10-year cumulative incidence of GI bleeding was 29.5% among aspirin users and 24.0% among nonusers (p = 0.016). The aspirin-treated group showed a significantly higher risk of GI bleeding than the untreated group (aHR = 1.20, 95% CI = 1.02-1.42; p = 0.029).
Conclusions:
In patients with HBV-related cirrhosis, the aspirin-treated group showed a significantly lower risk of HCC than the untreated group, whereas the risk of GI bleeding was significantly higher in the aspirin-treated group.
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