Skip to content

Clinical application of transcatheter arterial chemoembolization (TACE) before liver transplantation for hepatocellular carcinoma

Clinical application of transcatheter arterial chemoembolization (TACE) before liver transplantation for hepatocellular carcinoma

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900023965
Enrollment
Unknown
Registered
2019-06-19
Start date
2019-06-10
Completion date
Unknown
Last updated
2019-06-26

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

Conditions

Hepatocellular Carcinoma

Interventions

Group 1:Liver transplantation after DEB-TACE

Sponsors

Shulan (Hangzhou) Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Meet the Hangzhou Standard: (1) No portal vein cancer thrombus; (2) The cumulative diameter of tumors is less than 8 cm or the cumulative diameter of tumor, or the cumulative diameter is 8 cm, the preoperative alpha-fetoprotein (AFP) 400 ng/ml, and the histological graded be high or moderately differentiated primary hepatocellular carcinoma; 2. Complete preoperative laboratory examinations, enhanced CT and/or MRI imaging of the liver were available. 3. Child Pugh liver function rating: A or better B (< 7 points); 4. ECOG PS score: 0.2; 5. Subjects volunteered to join the study, signed informed consent, good compliance, with follow-up.

Exclusion criteria

Exclusion criteria: 1. Patients with hepatobiliary cell carcinoma and metastatic hepatocellular carcinoma; 2. Those who have received surgery and RFA before; 3. BCLC stage 0 and A; 4. Child-Pugh liver function rating C or worse B (7 points); 5. Imaging findings such as CT or MRI suggest significant distant metastasis; 6. Complicated with severe infections such as liver abscess; 7. Patients with other malignant tumors that have not been effectively controlled; 8. patients with HIV infection; 9. Researchers judge other situations that may affect the conduct of clinical research and the outcome of research.

Design outcomes

Primary

MeasureTime frame
disease-free survival rate;

Secondary

MeasureTime frame
Overall survival;disease control rate;objective response rate;

Countries

China

Contacts

Public ContactCao Guohong

Shulan (Hangzhou) Hospital

caoguohong@163.com+86 13958141275

Outcome results

None listed

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