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Evaluation of the efficacy of neoadjuvant therapy and direct surgical resection in patients with resectable liver cancer with portal vein thrombus

Evaluation of the efficacy of neoadjuvant therapy and direct surgical resection in patients with resectable liver cancer with portal vein thrombus

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108052
Enrollment
Unknown
Registered
2025-08-25
Start date
2025-08-25
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

Liver

Interventions

Treatment Group 1:First, neoadjuvant therapy was administered using transcatheter hepatic arterial infusion chemotherapy (HAIC) + sintilimab 200mg + bevacizumab 15mg/kg. After 1-2 cycles of treatment,
Treatment Group 2:Underwent direct surgical resection during initial presentation.

Sponsors

Department of Hepatobiliary Surgery, the First Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients who have undergone pathological examination or abdominal contrast-enhanced CT/MRI and meet the diagnostic criteria for hepatocellular carcinoma (HCC) as defined by China's 2022 Guidelines for the Diagnosis and Treatment of Primary Liver Cancer; 2. Patients with portal vein tumor thrombus (PVTT), classified as type I or II, and assessed by specialists as having resectable HCC; 3. Previously untreated patients; 4. Liver function classified as Child-Pugh grade A or B, and an Eastern Cooperative Oncology Group Performance Status (ECOG PS) score of <2; 5. Patients who have been fully informed about various treatment options, demonstrate good compliance with outpatient follow-up, and have complete follow-up data.

Exclusion criteria

Exclusion criteria: 1. Patients with organic diseases of major organs such as the heart, brain, or kidneys, or those with concurrent malignancies; 2. Patients who have previously undergone treatment for liver cancer; 3. Patients with decompensated liver disease (Child-Pugh grade C); 4. Patients with incomplete or missing clinical data; 5. Patients with poor medication compliance, or women who are pregnant or lactating.

Design outcomes

Primary

MeasureTime frame
Recurrence-Free Survival (RFS);Overall Survival (OS);

Countries

China

Contacts

Public ContactLan Xiang

Department of Hepatobiliary Surgery, the First Hospital of Chongqing Medical University

lanxiangkeyan@163.com+86 136 2978 0427

Outcome results

None listed

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