Long-term follow-up of treatment-naïve HBeAg-negative patients with chronic hepatitis B

Ir J Med Sci. 2023 Apr;192(2):633-639. doi: 10.1007/s11845-022-03066-y. Epub 2022 Jun 18.

Abstract

Background/aims: We aimed to explore long-term results of oral antiviral agents in treatment-naïve "HBeAg negative chronic hepatitis B (CHB)" and determine the factors affecting the complete virological response.

Method: Patients with HBeAg-negative CHB who used oral antiviral agents for at least 3 years were evaluated retrospectively.

Results: A total of 173 patients were recorded. The mean duration of treatment was 62.2 ± 28.9 months. Complete virological responses (CVR) were 82.8% (n = 53/64) in tenofovir disoproxil fumarate (TDF), 84.4% (n = 49/58) in lamivudine (LAM), 83.9% (n = 26/31) in entecavir (ETV), 95% in telbivudine (LdT) (n = 19/20) (p = 0.290). Multivariate analysis revealed age ≤ 40 (p = 0.012, 95%CI = 1.38-13.76, OR = 4.36) and baseline HBV DNA value (p = 0.003, 95%CI = 1.23-2.63, OR = 1.78) as independent factors for CVR. Virological breakthrough was detected in 29 (50%) patients on LAM therapy, two (6.4%) patients on ETV therapy, and two (10%) patients on LdT therapy. Treatment was switched to another antiviral agent due to osteoporosis in four patients in the TDF group, muscle pain in nine patients in the LDT group, and headache in one patient in the ETV group. Hepatocelluler cancer was detected in five patients. HBsAg seroclearance developed in two patients. Anti-HBs seroconversion was not detected.

Conclusion: CVR was achieved at similar rates with all four antiviral agents, while younger age (≤ 40) and low baseline viral load were the main factors for virological response. However, drug resistance and virological breakthrough in the LAM group and side effects in the LdT group were detected during the long-term follow-up. Moreover, HBsAg seroclearance was achieved at very low rates with oral antiviral agents.

Keywords: Antiviral agents; Chronic hepatitis B; Entecavir; Lamivudine; Tenofovir disoproxil fumarate; Virological response.

MeSH terms

  • Antiviral Agents / adverse effects
  • Antiviral Agents / therapeutic use
  • DNA, Viral / pharmacology
  • DNA, Viral / therapeutic use
  • Follow-Up Studies
  • Hepatitis B Surface Antigens / pharmacology
  • Hepatitis B Surface Antigens / therapeutic use
  • Hepatitis B e Antigens / pharmacology
  • Hepatitis B e Antigens / therapeutic use
  • Hepatitis B virus / genetics
  • Hepatitis B, Chronic* / drug therapy
  • Humans
  • Retrospective Studies
  • Tenofovir / pharmacology
  • Tenofovir / therapeutic use
  • Treatment Outcome
  • Viral Load

Substances

  • Hepatitis B e Antigens
  • Hepatitis B Surface Antigens
  • Tenofovir
  • Antiviral Agents
  • DNA, Viral