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Prognosis Comparison Between Chronic Hepatitis B Patients Receiving a Finite Course of Tenofovir and Entecavir Treatment: A Nationwide Cohort Study in Taiwan

  • Chih Lang Lin
  • , Yi Lan Lin
  • , Kung Hao Liang
  • , Li Wei Chen
  • , Cheng Hung Chien
  • , Ching Chih Hu
  • , Ting Shuo Huang
  • , Yu Chiau Shyu
  • , Chau Ting Yeh*
  • , Rong Nan Chien
  • *Corresponding author for this work
  • Chang Gung Memorial Hospital
  • Chang Gung University
  • Mackay Memorial Hospital Taiwan
  • Veterans General Hospital-Taipei
  • National Yang Ming Chiao Tung University
  • Chang Gung University of Science and Technology
  • Academia Sinica - Institute of Molecular Biology

Research output: Contribution to journalJournal Article peer-review

4 Scopus citations

Abstract

Purpose: Entecavir (ETV) and tenofovir disoproxil fumarate (TDF) are both recommended as first-line treatments for patients with chronic hepatitis B virus (CHB) infection according to international HBV treatment guidelines. However, recent studies reported conflicting results regarding the preferred antiviral in the prevention of hepatocellular carcinoma (HCC). This cohort study aimed to investigate this issue by using Taiwan's National Health Insurance Research Database, wherein a “finite” but not life-long treatment policy was applied. Methods: From January 2008 to December 2013, a total of 12,388 consecutive adult patients with CHB who received a finite course of TDF treatment (n = 1250) or ETV treatment (n = 11,138) were analyzed through screening for study eligibility followed by the 1:4 propensity score matching method. Findings: In the entire cohort, the annual incidence and survival between the ETV and TDF groups were not significantly different regarding HCC occurrence (2.05 vs 2.74 per 100 patient-years [PY]; P = 0.055; hazard ratio [HR], 0.975; log-rank, P = 0.966), cirrhosis-related complications (1.9 vs 2.4 per 100 PY; P = 0.149; HR, 0.869; log-rank, P = 0.388), or all-cause mortality (2.16 vs 1.6 per 100 PY; P = 0.119; HR, 0.831; log-rank, P = 0.342), respectively. Propensity score matching analyses yielded similar results regarding HCC occurrence, cirrhosis-related complications, and all-cause mortality. In addition, these findings were consistently reproduced in the subgroups of patients with chronic hepatitis and cirrhosis that developed before antiviral treatment. Implications: ETV and TDF did not significantly differ in prevention of HCC occurrence or reduction of cirrhosis-related complications and all-cause mortality in patients with CHB receiving a finite period of treatment.

Original languageEnglish
Pages (from-to)403-423
Number of pages21
JournalClinical Therapeutics
Volume44
Issue number3
DOIs
StatePublished - 03 2022

Bibliographical note

Publisher Copyright:
© 2022 Elsevier Inc.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 1 - No Poverty
    SDG 1 No Poverty
  2. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • ETV
  • HCC
  • TDF
  • chronic hepatitis B
  • entecavir
  • hepatocellular carcinoma
  • tenofovir disoproxil fumarate

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