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Transarterial Chemoembolization for Unresectable Hepatocellular Carcinoma With Portal Vein Tumor Thrombosis

Transarterial Chemoembolization Versus Best Support for Unresectable Hepatocellular Carcinoma With Portal Vein Tumor Thrombosis

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00646100
Acronym
TACEHCC
Enrollment
164
Registered
2008-03-28
Start date
2007-07-31
Completion date
2010-02-28
Last updated
2012-06-06

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

Conditions

Hepatocellular Carcinoma

Keywords

hepatocellular carcinoma, transcatheter arterial chemoembolization, prospective control study, best support care, survival

Brief summary

Transcatheter arterial chemoembolization (TACE) had been proved to improve the survivals for middle stage hepatocellular carcinoma (HCC), but for advanced stage HCC its' efficacy had not been proved. The investigators hypothesize that TACE also improve the survivals for advanced stage HCC. Thus, the investigators carried out this prospective control study to find out if the survivals for patients after TACE better than only best support or not.

Interventions

PROCEDUREtranscatheter arterial chemoembolization

chemo-lipiodolization with EADM 50mg, Lobaplatin 50mg, and MMC 6mg,plus particleembolization.

Sponsors

Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* The diagnosis of HCC was based on the diagnostic criteria for HCC used by the European Association for the Study of the Liver (EASL) * Tumor size \>7 cm with a portal vein invasion, and the tumor was considered to be unresectable * No previous HCC directed treatment * Eastern Co-operative Group performance status 0-1 * Liver function: Child's A

Exclusion criteria

* Avascular tumor * Evidence of hepatic decompensation including ascites, gastrointestinal bleeding or hepatic encephalopathy * underlying serve cardiac or renal diseases * Known or suspected allergy to the investigational agent or any agent given in association with this trial * Diffuse-type HCC * For patients with main portal vein occlusion, no adequate collateral circulation around the occluded portal vein

Design outcomes

Primary

MeasureTime frame
survival rates6, 12 months

Secondary

MeasureTime frame
quality of life6, 12 months

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026