Entecavir for Chronic Hepatitis B in Hepatocellular Carcinoma Patients Underwent Radiofrequency Ablation Therapy

• Status: Unknown status
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

Summary

Persistent replication of HBV (47-55%) is frequently found in patients with HCC, which in turn leads to deterioration of liver reserve. Moreover, a large proportion of HCC patients who underwent curative therapy died from progressive liver decompensation rather than recurrence of cancer. It had been proved that anti-viral therapy for hepatitis C virus (HCV)-related HCC patients could reduce the rate of tumor recurrence after surgical resection.

This is a prospective study to evaluate the efficacy of ETV therapy in chronic hepatitis B patients after receiving RFA therapy for HCC.

• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Taipei Veterans General Hospital, Taiwan
• Treatments: Entecavir

Criteria

Inclusion Criteria:

• HCC diagnosed by pathology verification or in accordance with the guidelines of American Association for the Study of Liver Diseases published in 2010 (typical vascular pattern in computed tomography scan or magnetic resonance imaging study) ,

• Solitary tumor less than 5 cm in diameter or 2-3 tumors with the largest one no more than 3 cm in diameter,

• No extrahepatic metastasis,

• No radiological evidence of invasion into major portal vein or hepatic vein branches,

• Good liver reserve with Child-Pugh Class A or B,

• A platelet count of more than 50,000/mm3,

• Serum creatinine level ≤ 2 mg/dL,

• No previous treatment for HCC,

• Positive for serum hepatitis B surface antigen (HBsAg) for more than 6 months

• Positive serum HBV DNA using a Cobas Amplicor HBV monitor (Roche Diagnostic System, Basel, Switzerland).

Exclusion Criteria:

• Dual or multiple infections with hepatitis C virus, hepatitis D virus, or the human immunodeficiency virus,

• Other forms of liver disease such as alcoholic hepatitis, autoimmune hepatitis, Wilson's disease, hemochromatosis,

• Use of interferon alpha, thymosin or antiviral agents within 6 months preceding entry into the study,

• Women who are pregnant or nursing.