Skip to content

Adjuvant InterFeron After Curative Resection of HCV-related Hepatocellular Carcinoma in Elderly Patients: a Multicenter Randomized Controlled Trial

Adjuvant InterFeron After Curative Resection of HCV-related Hepatocellular Carcinoma in Elderly Patients: a Multicenter Randomized Controlled Trial - iFACT trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005455
Enrollment
300
Registered
2011-04-20
Start date
2011-04-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HCV-related hepato cellular carcinoma

Interventions

Adjuvant interferon alpha therapy. Three times of 3,000,000 units / a week. Close follow-up

Sponsors

Tokyo University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Ages between 61 and 77 years old 2) Primary HCC or recurrent HCC more than two years after previous therapy 3) Classical HCC 4) HCV chronic hepatitis or cirrhosis 5) No extrahepatic lesions 6) Fine or moderate organ function fulfilling the following criteria. 7) Child-Pugh score < 8 8) ECOG performance status 0-2 9) CES-D score <16 10) Written informed consent

Exclusion criteria

Exclusion criteria: 1) Positive HBs-Ag 2) Other anticancer treatment or interferon therapy within 3 months before surgery. 3) Specific drug which is forbidden in this trial is needed. 4) Participating in other clinical trial regarding HCC 5) Autoimmune hepatitis, alcoholic hepatitis, etc. 6) Allergy for specific biologics 7) Severe postoperative complications 8) Asthma 9) Diabetes requiring insulin therapy 10) Severe hypertension 11) Heart disease that complicates perioperative treatments 12) Interstitial pneumonia 13) Psychiatric disorder 14) Malignant disease in other organ within 5 years 15) Moderate or severe renal dysfunction (estimated Ccr < 30ml/min) 16) Other reason that an attending doctor considers

Design outcomes

Primary

MeasureTime frame
Recurence free survival

Countries

Japan

Contacts

Public ContactTakeaki Ishizawa

Tokyo University Hospital Hepato-Biliary-Pancreatic Surgery Division

kihase-tky@umin.ac.jp03-3815-5411

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026