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RCT of TAE Simultaneously Combined Thermal Ablation for Large Hepatocellular Carcinoma

Randomized Controlled Trial of Transarterial Embolization Simultaneously Combined Thermal Ablation for Large Hepatocellular Carcinoma

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02964260
Enrollment
410
Registered
2016-11-16
Start date
2016-05-31
Completion date
2022-12-31
Last updated
2021-05-14

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

Conditions

Hepatocellular Carcinoma, Adult

Keywords

HCC; Embolization; Ablation; simultaneously; sequentially

Brief summary

This study intends to evaluate the efficacy and safety of Transarterial embolization (TAE) simultaneously combined with thermal ablation for large hepatocellular carcinoma (HCC). Half participants will receive TAE simultaneously combined with thermal ablation and the other half receive TACE sequentially combined with thermal ablation, which is a conventional treatment for HCC patients.

Detailed description

The treatment method Transarterial chemoembolization (TACE) sequentially combined with thermal ablation is recommend for large HCC patients from NCCN Guideline and Chinese guideline Diagnosis and Treatment of Primary Liver Cancer. The details of this sequential method consist one or more times of TACE followed by thermal ablation at least one month later to make the tumor completely inactivate. The thermal ablations include multiple applicators radiofrequency or microwave ablations. However, this method includes such disadvantages. 1) The limitation of lipiodol dosage in one TACE session is 30ml so that many patients needs more sessions of TACE; (2) Lipiodol and chemical drugs is easy to leak when patients have hepatic arteriovenous fistula. (3) Repeated TACE could cause more serious side effects. (4) Tumors of many patients are still not controlled or grow too large to ablate after TACEs which increases the metastasis risk and affects the efficacy and survival time. However, TAE simultaneously combined with thermal ablation is another combination type which reduce the interval time between two procedures from one month to 1-3 days. TAE removes the chemical drugs and uses embolic agents such as Embosphere to obstruct vessels to enhance the effect of followed ablations. The main aim of reducing interval and remove chemical drugs is to make the tumor completely inactivate in one hospitalization like surgical operation, hoping bringing less side effects, better efficacy and longer survival time. Thus the investigators will launch a prospective, multicenter randomized controlled clinical trial to compare the 3-years overall survival, safety, social and economic benefit of TAE simultaneously combined with ablation and TACE sequentially combined with ablation. The investigators expect to acquire Ia-level evidence-based medical evidence which can be accepted by the clinical guideline, popularizing, demonstrating our therapy.

Interventions

DRUGChemotherapy drug

Doxorubicin/Platinum agents

DRUGEmbolic agents

Lipiodol/Gelatin sponge/PVA/Blank microspheres

PROCEDURESimultaneously

1-3 days

PROCEDURESequentially

1 month

DEVICEAblation

Radiofrequency ablation/Microwave ablation

Sponsors

First Affiliated Hospital, Sun Yat-Sen University
CollaboratorOTHER
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
CollaboratorOTHER
Third Affiliated Hospital, Sun Yat-Sen University
CollaboratorOTHER
Sixth Affiliated Hospital, Sun Yat-sen University
CollaboratorOTHER
Guangdong Provincial People's Hospital
CollaboratorOTHER
Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Age between 18 to 70 years with estimated survival over 3 months * Number of tumors \< 3 * Diameter of tumor between 5cm to 15cm * No portal vein trunk tumoral thrombus or inferior vena cava tumoral thrombus * With arteriovenous fistula or arterioportal shunt fistula that can be completely embolized * Child-Pugh class A or B/Child score \> 7;ECOG score \< 2 * Tolerable coagulation function or reversible coagulation disorders * Laboratory examination test: WBC≥3.0×10E9/L; Hb≥3.0×10E9/L; PLT ≥50×10E9/L; INR \< 2.3 or PT\< 16.5s; Cr ≤ 145.5 umul/L * Signed informed consent before recruiting

Exclusion criteria

* Diffused HCC * With portal vein trunk tumoral thrombus * With inferior vena cava tumoral thrombus or hepatic vein tumor thrombus * With lymphatic metastasis or extra hepatic metastasis * Child-Pugh class C and can't be improved by expectant treatment * Untreatable coagulation disorders, severe hemogram abnormal and bleeding tendency * Massive intractable ascites * ECOG score \> 2

Design outcomes

Primary

MeasureTime frameDescription
Overall survival3 yearsFrom complete remission of the index large tumor to patient death or the completion of this trial

Secondary

MeasureTime frameDescription
Recurrence free survival3 yearsFrom complete remission of the index large tumor to tumor recurrence either in- or extra- hepatic or the completion of this trial
liver and renal function3 yearsAlanine aminotransferase,Ast,total bilirubin,albumin,creatinine,Urea nitrogen
Complications3 yearsnumber of participants with Complications
Times of interventional procedures3 yearsThe number of procedures for each patient, either TACE/TAE or ablation

Countries

China

Contacts

Primary ContactJinhua Huang, Ph.D
huangjh@sysucc.org.cn0086-20-87343272

Outcome results

None listed

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