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Efficacy and Safety Analysis of Temperature-Sensitive Liquid Embolic Agent-TACE Versus Drug-Eluting Bead-TACE in the Treatment of Unresectable Hepatocellular Carcinoma: A Multicenter, Retrospective Cohort Study

Efficacy and Safety Analysis of Temperature-Sensitive Liquid Embolic Agent-TACE Versus Drug-Eluting Bead-TACE in the Treatment of Unresectable Hepatocellular Carcinoma: A Multicenter, Retrospective Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113198
Enrollment
Unknown
Registered
2025-11-26
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Unresectable hepatocellular carcinoma (HCC)

Interventions

Observation group:None

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Pathologically or clinically diagnosed with hepatocellular carcinoma (HCC) and unresectable; (2) Aged 18–75 years; (3) At least one measurable lesion per mRECIST 1.1 criteria; (4) Liver function classified as Child-Pugh Grade A or B [see Child-Pugh Classification Criteria (Table 1)]; (5) Complete clinical and follow-up data.

Exclusion criteria

Exclusion criteria: (1) No CT or MRI imaging data available before TACE treatment or 1 month after surgery; (2) Cases lost to follow-up within 1 month after TACE treatment; (3) Patients with extrahepatic metastasis or concurrent other tumors; (4) Severe liver dysfunction, uncorrectable coagulation disorders, complete obstruction of the main portal vein by tumor thrombus, or significant reduction in peripheral blood leukocytes and platelets (WBC < 3.0×10^9/L, PLT < 50×10^9/L) at the time of treatment; (5) Concurrent severe cardiorenal insufficiency, etc.

Design outcomes

Secondary

MeasureTime frame
Overall survival (OS);Progression-free survival (PFS);Duration of ongoing remission (DOR);Disease Control Rate (DCR);Safety;

Primary

MeasureTime frame
Overall survival (OS);

Countries

China

Contacts

Public ContactChang Liu

West China Hospital of Sichuan University

westchina_lc@foxmail.com+86 189 8060 6382

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 13, 2026