» Articles » PMID: 10207807

Interferon Therapy Lowers the Rate of Progression to Hepatocellular Carcinoma in Chronic Hepatitis C but Not Significantly in an Advanced Stage: a Retrospective Study in 1148 Patients. Viral Hepatitis Therapy Study Group

Overview
Journal J Hepatol
Publisher Elsevier
Specialty Gastroenterology
Date 1999 Apr 20
PMID 10207807
Citations 48
Authors
Affiliations
Soon will be listed here.
Abstract

Background/aim: Hepatocellular carcinoma frequently develops during the advanced stages of chronic hepatitis C. We examined whether interferon prevents the development of hepatocellular carcinoma in chronic hepatitis C patients.

Methods: Japanese patients with chronic hepatitis C (n = 1.148; 117 with portal fibrous expansion (F1), 636 with bridging fibrosis (F2), 355 with bridging fibrosis and architectural distortion (F3)) and 40 cirrhotic (F4) patients were treated with interferon. These patients were followed from 1 to 7 years after interferon therapy. Blood tests and image analysis were serially performed to assess response to interferon and to detect hepatocellular carcinoma. Fifty-five cirrhotic type C patients (control F4) not receiving interferon were enrolled in this study.

Results: Sustained (SR: 27.5%) and transient (TR: 23.0%) responders totaled 50.5%, while 49.5% did not respond to interferon. SR showed an improvement in disease stage reflected by increased platelet counts. Fifty-two patients (9 F2, 36 F3, and 7 F4) developed hepatocellular carcinoma in the follow-up period; 3 SR, 8 TR, and 41 non-responders (NR). The cumulative incidence of hepatocellular carcinoma in F2 was significantly lower (p = 0.019) in SR compared with NR, but not in SR in F3 and F4 patients. However, the cumulative incidence of hepatocellular carcinoma was significantly decreased in all SR (p = 0.0001) and TR (p = 0.0397) compared with all NR.

Conclusion: These results indicate that interferon therapy in chronic hepatitis C patients lowered the rate of progression of hepatocellular carcinoma in sensitive cases but not in patients in an advanced stage.

Citing Articles

Histological improvement of fibrosis in patients with hepatitis C who achieved a 5-year sustained virological response to treatment with direct-acting antivirals.

Iwamoto T, Nozaki Y, Inoue T, Suda T, Mizumoto R, Arimoto Y J Gastroenterol. 2024; 60(2):197-209.

PMID: 39585387 PMC: 11794422. DOI: 10.1007/s00535-024-02165-0.


Impact of eradication of hepatitis C virus on liver-related and -unrelated diseases: morbidity and mortality of chronic hepatitis C after SVR.

Nakagawa M, Asahina Y, Kakinuma S, Okamoto R J Gastroenterol. 2022; 58(4):299-310.

PMID: 36585501 DOI: 10.1007/s00535-022-01940-1.


Characteristics of hepatocellular carcinoma in patients with hepatitis C virus who received direct-acting antiviral therapy and achieved sustained virological response: The impact of a hepatologist on surveillance.

Tada T, Kumada T, Matono T, Nakamura S, Sue M, Matsuo Y JGH Open. 2022; 6(7):462-469.

PMID: 35822120 PMC: 9260217. DOI: 10.1002/jgh3.12774.


General evaluation score for predicting the development of hepatocellular carcinoma in patients with advanced liver fibrosis associated with hepatitis C virus genotype 1 or 2 after direct-acting antiviral therapy.

Tada T, Kurosaki M, Tamaki N, Yasui Y, Mori N, Tsuji K JGH Open. 2022; 6(7):487-495.

PMID: 35822118 PMC: 9260214. DOI: 10.1002/jgh3.12778.


Real-world long-term analysis of daclatasvir plus asunaprevir in patients with hepatitis C virus infection.

Fujii H, Kimura H, Hasebe C, Akahane T, Satou T, Kusakabe A JGH Open. 2022; 6(5):344-352.

PMID: 35601120 PMC: 9120887. DOI: 10.1002/jgh3.12749.