Noninferiority Outcomes of Besifovir Compared to Tenofovir Alafenamide in Treatment-Naïve Patients with Chronic Hepatitis B

Gut Liver. 2024 Mar 15;18(2):305-315. doi: 10.5009/gnl220390. Epub 2024 Jan 12.

Abstract

Background/aims: : Besifovir dipivoxil maleate (BSV) and tenofovir alafenamide fumarate (TAF) have been recently approved in Korea as the initial antiviral agents for chronic hepatitis B (CHB). However, the real-world outcome data for these drugs remain limited. Therefore, we conducted a noninferiority analysis using real-world data to compare the clinical outcomes of the two nucleotide analogs in treatment-naïve patients with CHB.

Methods: : We retrospectively investigated a cohort of patients with CHB who received BSV or TAF as first-line antiviral agents. The endpoints were virological response (VR) and liver-related clinical outcomes.

Results: : A total of 537 patients, consisting of 202 and 335 patients administered BSV and TAF, respectively, were followed up for 42 months. No significant difference was observed between the VRs of the patients from the two groups. The rates of biochemical response, virologic breakthrough, and incidence rates of hepatocellular carcinoma did not differ between the groups. However, the hepatitis B e antigen seroclearance rate was higher and the renal function declined less in the BSV group. Multivariable analysis indicated older age, alcohol abuse, cirrhosis and ascites, and lower serum HBV DNA level to be independently associated with increased hepatocellular carcinoma risk. The 1:1 propensity score-matched analysis with 400 patients showed VR rates of 85.0% and 88.7% in the BSV and TAF group patients, respectively, at 2 years. The absolute value of the 95% confidence interval for the difference (-0.04 to 0.12) satisfied the a priori limit of a noninferiority of 0.15.

Conclusions: : BSV is noninferior to TAF in terms of VR, and their clinical outcomes are comparable to CHB.

Keywords: Besifovir; Carcinoma, hepatocellular; Hepatitis B, chronic; Prognosis; Tenofovir alafenamide.

MeSH terms

  • Adenine
  • Alanine
  • Antiviral Agents / therapeutic use
  • Carcinoma, Hepatocellular* / drug therapy
  • Guanine / analogs & derivatives*
  • Hepatitis B, Chronic*
  • Humans
  • Liver Neoplasms* / drug therapy
  • Organophosphonates*
  • Retrospective Studies
  • Tenofovir / therapeutic use
  • Treatment Outcome

Substances

  • Tenofovir
  • ((1-((2-amino-9H-purin-9-yl)methyl)cyclopropyl)oxy)methylphosphonic acid dipivoxyl
  • Antiviral Agents
  • Adenine
  • Alanine
  • Guanine
  • Organophosphonates

Grants and funding

ACKNOWLEDGEMENTS This work was supported by Korea University Research Grant.