4.7 Article

Inhibition of hepatocellular carcinoma by PegIFNα-2a in patients with chronic hepatitis C: a nationwide multicenter cooperative study

Journal

JOURNAL OF GASTROENTEROLOGY
Volume 48, Issue 3, Pages 382-390

Publisher

SPRINGER JAPAN KK
DOI: 10.1007/s00535-012-0641-9

Keywords

Chronic hepatitis C; Hepatocellular carcinoma; Peginterferon

Funding

  1. Japanese Ministry of Health, Welfare, and Labor
  2. Chugai Co.
  3. MSD Co.
  4. Grants-in-Aid for Scientific Research [25670366, 21590831, 24890058, 24590960, 24659368, 24590980] Funding Source: KAKEN

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We investigated whether the administration of maintenance doses of interferon prevented hepatocellular carcinoma (HCC) in patients with chronic hepatitis C. Study 1: A multicenter, retrospective, cooperative study was carried out to determine whether long-term administration of low-dose peginterferon alpha-2a (PegIFN alpha-2a) prevented HCC development in patients with chronic hepatitis C. In total, 594 chronic hepatitis C patients without a history of HCC were enrolled and treated with 90 mu g PegIFN alpha-2a administered weekly or bi-weekly for at least 1 year. Study 2: HCC developed in 16 of 99 additional patients without PegIFN alpha-2a treatment during 3.8 years of observation. A propensity-matched control study was then carried out to compare the incidence of HCC between the 59 patients who received low-dose PegIFN alpha-2a (PegIFN alpha-2a group) and 59 patients who did not receive PegIFN alpha-2a treatment (control group), matched for sex, age, platelet count, and total bilirubin levels. Study 1: HCC developed in 49 patients. The risk of HCC was lower in patients with undetectable hepatitis C virus RNA, a parts per thousand currency sign40 IU/L alanine aminotransferase (ALT), or a parts per thousand currency sign10 ng/L alpha-fetoprotein (AFP) 24 weeks after the start of therapy. Study 2: The incidence of HCC was significantly lower in the PegIFN alpha-2a group than in the control group. Low-dose and long-term maintenance administration of PegIFN alpha-2a decreased the incidence of HCC in patients with normalized ALT and AFP levels at 24 weeks compared with patients without normal ALT and AFP levels.

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