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Optimization of Sequential Surgical Treatment Strategies After Conversion Therapy for Initially Unresectable Hepatocellular Carcinoma and Assessment of Clinical Outcomes

Optimization of Sequential Surgical Treatment Strategies After Conversion Therapy for Initially Unresectable Hepatocellular Carcinoma and Assessment of Clinical Outcomes

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129178
Enrollment
Unknown
Registered
2026-07-31
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Hepatocellular carcinoma

Interventions

Sponsors

The First Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age between 18 and 80 years; 2.Patients diagnosed with initially unresectable hepatocellular carcinoma (uHCC) who received conversion therapy, including but not limited to oral or intravenous chemotherapy, transarterial chemoembolization (TACE), radiofrequency ablation (RFA), and yttrium-90 selective internal radiation therapy (Y-90 SIRT). 3.Evidence of tumor shrinkage and downstaging on preoperative imaging after conversion therapy. 4.Undergone hepatic resection. 5.Completed preoperative assessment and three-dimensional reconstruction, with estimated future liver remnant volume meeting the criteria for anatomical liver resection. 6.Complete clinical data available.

Exclusion criteria

Exclusion criteria: 1.Failure to meet the above inclusion criteria. 2.Severe cardiac, hepatic, or renal insufficiency, or severe malnutrition not correctable by medical therapy. 3.Tumor with complete invasion or encasement of major vessels, or presence of tumor thrombus. 4.Evidence of intra-abdominal or distant metastasis. 5.Pregnancy, lactation, or planned pregnancy in women of childbearing age. 6.Other conditions deemed unsuitable for enrollment by the investigators.

Design outcomes

Primary

MeasureTime frame
Survival and Recurrence Endpoints;

Secondary

MeasureTime frame
Perioperative Complications;Intraoperative Variables;

Countries

China

Contacts

Public ContactShuguo Zheng

The First Affiliated Hospital of Army Medical University

shuguozh@163.com+86 23 68765706

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026