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. 2020 Aug 28;26(4):411–429. doi: 10.3350/cmh.2020.0049

Table 4.

Comparison of treatment indicators for patients with liver cirrhosis

KASL AASLD EASL APASL
Compensated cirrhosis 1) Treat if HBV DNA level is ≥2,000 IU/mL, regardless of the ALT level 1) Treat if HBV DNA is >2,000 IU/mL, regardless of the ALT level 1) Treat for any detectable HBV DNA, regardless of the ALT levels, in patients with compensated or decompensated cirrhosis 1) Treat if HBV DNA is >2,000 IU/mL, even if the ALT levels are normal
1) Treat
2) Consider 2) Treatment can be considered if HBV DNA is detectable but low (<2,000 IU/mL), regardless of the ALT level 2) Treat patients with low level viremia (HBV DNA <2,000 IU/mL), regardless of the ALT level 2) Treatment can be considered irrespective of HBV DNA and ALT levels
Decompensated cirrhosis 1) Treat with a NA if serum HBV DNA is detected, regardless of the ALT level 1) Treat with antiviral therapy indefinitely, regardless of the HBV DNA level, HBeAg, or ALT level 1) Immediately treat with a NA with high barrier to resistance, irrespective of the HBV replication level 1) Immediately treat with a NA for patients with detectable HBV DNA
1) Treat 2) Consider liver transplantation 2) Consider liver transplantation 2) Assess for the possibility of liver transplantation 2) Consider treatment for all patients with hepatic decompensation, irrespective of HBV DNA levels
2), 3) Consider 3) Consider liver transplantation
First-line agents* Entecavir, tenofovir DF, tenofovir AF, besifovir Entecavir, tenofovir DF, tenofovir AF Entecavir, tenofovir DF, tenofovir AF Entecavir, tenofovir DF

KASL, Korean Association for the Study of the Liver; APASL, Asian-Pacific Association for the Study of the Liver; HBV, hepatitis B virus; ALT, alanine aminotransferase; NA, nucleos(t)ide analog; HBeAg, hepatitis B e antigen; tenofovir DF, tenofovir disoproxil fumarate; tenofovir AF, tenofovir alafenamide fumarate.

*

Peg-interferon can only be used, with caution, for compensated cirrhosis, but may not be preferred owing to safety concerns.

Insufficient data for decompensated cirrhosis.