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Hepatocellular carcinoma, decompensation, and mortality based on hepatitis C treatment: A prospective cohort study

  • Gwang Hyeon Choi
  • , Eun Sun Jang
  • , Young Seok Kim
  • , Youn Jae Lee
  • , In Hee Kim
  • , Sung Bum Cho
  • , Han Chu Lee
  • , Jeong Won Jang
  • , Moran Ki
  • , Hwa Young Choi
  • , Dahye Baik
  • , Sook Hyang Jeong*
  • *Corresponding author for this work
  • Seoul National University
  • Soonchunhyang University
  • Inje University
  • Chonnam National University
  • University of Ulsan
  • The Catholic University of Korea
  • National Cancer Center Korea

Research output: Contribution to journalJournal articlepeer-review

Abstract

BACKGROUND Prospective studies of the long-term outcomes of patients with hepatitis C virus (HCV) infection after treatment with interferon-based therapy (IBT) or direct-acting antivirals (DAA) are limited in many Asian countries. AIM To elucidate the incidences of hepatocellular carcinoma (HCC) and death/transplantation based on treatment with IBT or DAA, to compare the outcomes of the sustained virologic response (SVR) to IBT and DAA, and to investigate outcome-determining factors after SVR. METHODS This cohort included 2054 viremic patients (mean age, 57 years; 46.5% male; 27.4% with cirrhosis) prospectively enrolled at seven hospitals between 2007 and 2019. They were classified as the untreated group (n = 619), IBT group (n = 578), and DAA group (n = 857). Outcomes included the incidences of HCC and death/transplantation. The incidences of the outcomes for each group according to treatment were calculated using an exact method based on the Poisson distribution. A multivariate Cox regression analysis was performed to determine the factors associated with HCC or death/transplantation, followed by propensity score matching to confirm the results. RESULTS During a median of 4.1 years of follow-up, HCC and death/transplantation occurred in 113 and 206 patients, respectively, in the entire cohort. Compared with the untreated group, the incidences of HCC and death/transplantation were significantly lower in the IBT group [adjusted hazard ratio (aHR) 0.47, 95%CI: 0.28-0.80 and aHR 0.28, 95%CI: 0.18-0.43, respectively] and the DAA group (aHR 0.58, 95%CI: 0.35-0.96, and aHR 0.19, 95%CI: 0.20-0.68, respectively). Among 1268 patients who attained SVR with IBT (n = 451) or DAA (n = 816), the multivariable-adjusted analysis showed no differences in the risks of HCC (HR 2.03; 95%CI: 0.76-5.43) and death/transplantation (HR 1.38; 95%CI: 0.55-3.49) between the two groups. This was confirmed by a propensity score-matching analysis. Independent factors for HCC after SVR were age, genotype 1, and the presence of cirrhosis. CONCLUSION Treatment and achieving SVR with either IBT or DAA significantly reduced the incidences of HCC and mortality in the Asian patients with HCV infection. The risks of HCC and mortality were not significantly different regardless of whether SVR was induced by IBT or DAA.

Original languageEnglish
Pages (from-to)4019-4234
Number of pages216
JournalWorld Journal of Gastroenterology
Volume28
Issue number30
DOIs
StatePublished - 2022.08.14

UN SDGs

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

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Direct-acting antiviral
  • Hepatitis C virus
  • Hepatocellular carcinoma
  • Mortality
  • Sustained virologic response

Quacquarelli Symonds(QS) Subject Topics

  • Medicine

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