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Analysis of the efficacy of preoperative interventional therapy combined with systemic therapy in resectable hepatocellular carcinoma patients with high-risk recurrence

Analysis of the efficacy of preoperative interventional therapy combined with systemic therapy in resectable hepatocellular carcinoma patients with high-risk recurrence

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500104502
Enrollment
Unknown
Registered
2025-06-18
Start date
2024-06-15
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Hepatocellular carcinoma

Interventions

Direct surgery group:None

Sponsors

The First Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Clinically diagnosed or postoperative pathological diagnosis of hepatocellular carcinoma; 2) Resectable primary liver cancer at CNLC stage Ib and IIa; no liver cirrhosis with residual liver volume > 30% or with liver cirrhosis and residual liver volume > 40%; 3) Aged 18-75 years old, good surgical tolerance; Eastern Cooperative Oncology Group performance status score (ECOG PS) 0-1; Child-Pugh A grade, or grade B during the first hospitalization and converted to grade A after treatment; 4) With one or more of the following high-risk recurrence factors: a. Single large HCC (tumor size >= 10 cm); b. Unifocal multifocal disease (2-3 tumors, 1 tumor >= 5 cm); c. AFP >= 400 ng/ml; d. Tumor adjacent to major vascular structures (including the main portal vein, main hepatic vein and inferior vena cava), resulting in a resection margin < 1 cm; 5) The neoadjuvant treatment group underwent at least one interventional treatment and regular anti-angiogenic targeted therapy or immune checkpoint inhibitor therapy before surgical R0 resection.

Exclusion criteria

Exclusion criteria: 1) HCC combined with intrahepatic cholangiocarcinoma; having other malignant tumors except liver cancer within the past 5 years; 2) preoperative tumor rupture and bleeding; 3) having received other anti-tumor treatments before treatment, such as radiofrequency ablation, radiotherapy, systemic treatment, chemotherapy, etc.; 4) the surgery did not achieve R0 resection or ablation treatment was performed on small lesions during the operation; 5) the tumor is operable, but the family refuses the surgery or the data is incomplete.

Design outcomes

Primary

MeasureTime frame
Disease free survival;

Secondary

MeasureTime frame
Overall survival;Objective response rate;

Countries

China

Contacts

Public ContactJianfeng Li

The First Affiliated Hospital of Nanchang University

ndyfy01989@ncu.edu.cn+86 138 7008 8192

Outcome results

None listed

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