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The comparison between Entecavir and Tenofovir on overall survial of patients with HBV-related hepatocellular carcinoma after curative resection-- a retrospective cohort research

The comparison between Entecavir and Tenofovir on overall survial of patients with HBV-related hepatocellular carcinoma after curative resection-- a retrospective cohort research

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300070485
Enrollment
Unknown
Registered
2023-04-13
Start date
2022-05-04
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

HBV-related hepatocellular carcinoma

Interventions

TDF Group:None

Sponsors

The Third Affiliated Hospital of Naval Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Histopathologically confirmed hepatitis B associated hepatocellular carcinoma in patients aged 18-80 years with hepatitis B associated hepatocellular carcinoma; 2. Radical surgical resection was performed (no tumor residue was found in the remaining liver and other parts, and no tumor cells were found in the pathological margin); 3. Start receiving ETV or TDF as antiviral therapy before surgery or within 1 month after surgery; 4. Continuous antiviral therapy after surgery.

Exclusion criteria

Exclusion criteria: 1. There are other histopathological tumors other than hepatocellular carcinoma; 2. History of antiviral therapy other than TDF and ETV; 3. Other types of hepatitis B virus infection; 4. Patients with portal vein cancer thrombus or hepatic vein cancer thrombus or extrahepatic metastasis; 5. Follow-up time was less than 3 months; 6. Patients who have received antiviral therapy for more than 3 months before the diagnosis of HBV-associated HCC or started antiviral therapy for more than 1 month after surgery; 7. Patients with hepatectomy and tumor ablation.

Design outcomes

Primary

MeasureTime frame
date of recurrence;date of death;anti-viral drugs for HBV;

Secondary

MeasureTime frame
age;sex;HbsAg;HbsAb;HbeAg;HbeAb;HbcAb;HBV-DNA;alpha-fetoprotein;platelets;total bilirubin;alanine aminotransferase;albumin;prothrombin time;tumor diameter;multiple tumors;tumor capsule;cirrhosis degrees;resection margin;microvascular invasion;date of operation;intraoperative blood loss volume;intraoperative blood transfusion volume;

Countries

China

Contacts

Public ContactHuang Gang

The Third Affiliated Hospital of Naval Medical University

squaror@163.com+86 139 1866 3457

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026