Published online Jan 27, 2021. doi: 10.4254/wjh.v13.i1.144
Peer-review started: August 31, 2020
First decision: November 3, 2020
Revised: November 16, 2020
Accepted: November 28, 2020
Article in press: November 28, 2020
Published online: January 27, 2021
Processing time: 148 Days and 9 Hours
The oral nucleos(t)ide analogue, entecavir (ETV) was demonstrated to reduce the rate of hepatocellular carcinoma (HCC) in patients with hepatitis B virus (HBV)-associated liver cirrhosis. However, the reduction of HCC differs in various regions of the world.
To investigate the reduction of HCC development due to ETV therapy by meta-analysis.
We surveyed the differences in HCC development following ETV treatment based on published articles using PubMed (2004-2019).
The regions with the most marked reduction in HCC development due to ETV therapy were Spain (1.0%/year) and Canada (Southern part, 1.3%/year), and the most ineffective areas were South Korea (3.6%-3.8%/year), China (3.3%/year), Taiwan (2.4%-3.1%/year), and Hong Kong (2.8%/year). Following ETV administration, the incidence of HCC in genotype D regions (1.89% ± 0.28%/year, mean ± SE) was significantly lower than that in genotype C regions (2.91% ± 0.24%/year, P < 0.01). With regard to the initial HBV-DNA level, in genotype C patients (average: 5.61 Log10IU/mL) this was almost the same as that in genotype D patients (average: 5.46 Log10IU/mL). Moreover, there was no association between the prevalence ratio of HBV and the incidence of HCC on ETV treatment.
The effectiveness of ETV in preventing HCC development in HBV-associated liver cirrhosis is genotype-dependent.
Core Tip: Entecavir was demonstrated to reduce the rate of hepatocellular carcinoma (HCC) in patients with hepatitis B virus (HBV)-associated liver cirrhosis. The reduction of HCC differs in various regions of the world. We surveyed these differences based on published articles using PubMed (2004-2019). Following entecavir administration, the incidence of HCC in genotype D regions (1.89% ± 0.28%/year, mean ± SE) was significantly lower than that in genotype C regions (2.91% ± 0.24%/year, P < 0.01). The initial HBV-DNA level in genotype C patients was almost the same as that in genotype D patients. The effectiveness of entecavir in preventing HCC development in patients with HBV-associated liver cirrhosis is genotype-dependent.