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Published on: September 30, 2021
A cohort study to investigate hepatocellular carcinoma risk in hepatitis C patients
Chun-Hsiang Wang1, Lein-Ray Mo, Kuo-Kwan Chang
1Department of Hepato-gastroenterology, Tainan Municipal Hospital, Tainan, Taiwan. chunhsiang@gmail.com
Insights
Male gender, older age, and hepatitis C virus genotype 1b are key factors in developing liver cancer (HCC) in patients with chronic hepatitis C (HCV). These risk factors are crucial for understanding HCC progression in endemic areas.
Area of Science:
- Hepatology
- Viral Hepatitis
- Oncology
Background:
- Hepatocellular carcinoma (HCC) is a common complication of chronic hepatitis C (HCV) infection.
- Identifying risk factors for HCC development in HCV patients is crucial for proactive management.
Purpose of the Study:
- To identify clinical and laboratory factors associated with HCC development.
- To analyze risk factors in a longitudinal follow-up of chronic HCV patients.
Main Methods:
- Prospective follow-up of 164 chronic HCV patients from 2000-2008.
- Regular monitoring included liver function tests, alpha-fetoprotein levels, and abdominal ultrasounds.
Main Results:
- HCC developed in 11.6% of patients over the follow-up period.
- Significant risk factors for HCC included male gender, HCV genotype 1b, cirrhosis, and age over 65.
- Patients with HCV RNA levels >= 1 million copies/mL had a 2.7-fold increased risk of HCC.
Conclusions:
- Male gender, older age, and HCV genotype 1b are significant predictors of HCC development.
- These factors are important for risk stratification in chronic HCV patients.
- Understanding these risk factors aids in managing HCC progression, particularly in hepatitis B-endemic regions.
Background/Aims:
Hepatocellular carcinoma (HCC) frequently occurs with chronic hepatitis C (HCV) infection. This study tried to identify clinical and laboratory factors affecting development of HCC in a longitudinal follow-up of chronic HCV patients.
Methodology:
A total of 373 patients with CHC who were HCV RNA-seropositive were recruited during 2000-2003. The remaining 164 patients after application of exclusion criteria (90 males; 74 females; mean age: 58.2 +/- 14y/o) were prospectively recruited and followed-up with periodic liver function tests, alfa-fetoprotein and abdominal ultrasound examinations.
Results:
During follow-up between January 2000 and May 2008, HCC was identified in 19 (11.6%) patients. The incidence rate of HCC was 14.5/1,000 person-years. Fifteen patients (9.1%) developed a cirrhotic liver. Male gender (p=0.018), genotype 1b (p=0.034), cirrhosis (p<0.001) and older age (> or = 65y/o) (p=0.02) are significant risk factors for HCC. Overall, there was 2.7-fold increased risk in patients with HCV RNA > or = 1 million copies/mL to develop HCC. The incidence rate of HCC was 8.8% for pegIFNa/RBV-treated patients with sustained viral response and 14.3% for untreated patients (p=0.352).
Conclusions:
This cohort study highlights the roles of male gender, older age and genotype 1b in the progression from chronic HCV to HCC in an area endemic for hepatitis B.
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