RCT of TAE Simultaneously Combined Thermal Ablation for Large Hepatocellular Carcinoma
Primary Purpose
Hepatocellular Carcinoma, Adult
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Chemotherapy drug
Embolic agents
Simultaneously
Sequentially
Ablation
Sponsored by

About this trial
This is an interventional treatment trial for Hepatocellular Carcinoma, Adult focused on measuring HCC; Embolization; Ablation; simultaneously; sequentially
Eligibility Criteria
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
Sites / Locations
- Sun Yat-sen University Cancer CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
TAE combined ablation simultaneously
TACE combined ablation sequentially
Arm Description
TAE simultaneously combined with ablation.The treatment interval is 1-3 days between two procedures. TAE using embolic agents(Lipiodol/Gelatin sponge/PVA particles(300~500μm)/Blank microspheres).
TACE sequentially combined thermal ablation.The treatment interval is 1 month between two procedures. TACE using chemotherapy drug(Doxorubicin/platinum agents) and embolic agents(Lipiodol/Gelatin sponge/PVA particles(300~500μm)/Blank microspheres).
Outcomes
Primary Outcome Measures
Overall survival
From complete remission of the index large tumor to patient death or the completion of this trial
Secondary Outcome Measures
Recurrence free survival
From complete remission of the index large tumor to tumor recurrence either in- or extra- hepatic or the completion of this trial
liver and renal function
Alanine aminotransferase,Ast,total bilirubin,albumin,creatinine,Urea nitrogen
Complications
number of participants with Complications
Times of interventional procedures
The number of procedures for each patient, either TACE/TAE or ablation
Full Information
NCT ID
NCT02964260
First Posted
November 9, 2016
Last Updated
May 13, 2021
Sponsor
Sun Yat-sen University
Collaborators
First Affiliated Hospital, Sun Yat-Sen University, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, Third Affiliated Hospital, Sun Yat-Sen University, Sixth Affiliated Hospital, Sun Yat-sen University, Guangdong Provincial People's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02964260
Brief Title
RCT of TAE Simultaneously Combined Thermal Ablation for Large Hepatocellular Carcinoma
Official Title
Randomized Controlled Trial of Transarterial Embolization Simultaneously Combined Thermal Ablation for Large Hepatocellular Carcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
May 2021
Overall Recruitment Status
Unknown status
Study Start Date
May 2016 (Actual)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
December 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sun Yat-sen University
Collaborators
First Affiliated Hospital, Sun Yat-Sen University, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University, Third Affiliated Hospital, Sun Yat-Sen University, Sixth Affiliated Hospital, Sun Yat-sen University, Guangdong Provincial People's Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma, Adult
Keywords
HCC; Embolization; Ablation; simultaneously; sequentially
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
410 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
TAE combined ablation simultaneously
Arm Type
Experimental
Arm Description
TAE simultaneously combined with ablation.The treatment interval is 1-3 days between two procedures. TAE using embolic agents(Lipiodol/Gelatin sponge/PVA particles(300~500μm)/Blank microspheres).
Arm Title
TACE combined ablation sequentially
Arm Type
Other
Arm Description
TACE sequentially combined thermal ablation.The treatment interval is 1 month between two procedures. TACE using chemotherapy drug(Doxorubicin/platinum agents) and embolic agents(Lipiodol/Gelatin sponge/PVA particles(300~500μm)/Blank microspheres).
Intervention Type
Drug
Intervention Name(s)
Chemotherapy drug
Other Intervention Name(s)
Chemotherapy
Intervention Description
Doxorubicin/Platinum agents
Intervention Type
Drug
Intervention Name(s)
Embolic agents
Other Intervention Name(s)
Embolization
Intervention Description
Lipiodol/Gelatin sponge/PVA/Blank microspheres
Intervention Type
Procedure
Intervention Name(s)
Simultaneously
Other Intervention Name(s)
Treatment interval
Intervention Description
1-3 days
Intervention Type
Procedure
Intervention Name(s)
Sequentially
Other Intervention Name(s)
Treatment interval
Intervention Description
1 month
Intervention Type
Device
Intervention Name(s)
Ablation
Other Intervention Name(s)
RFA/MWA
Intervention Description
Radiofrequency ablation/Microwave ablation
Primary Outcome Measure Information:
Title
Overall survival
Description
From complete remission of the index large tumor to patient death or the completion of this trial
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Recurrence free survival
Description
From complete remission of the index large tumor to tumor recurrence either in- or extra- hepatic or the completion of this trial
Time Frame
3 years
Title
liver and renal function
Description
Alanine aminotransferase,Ast,total bilirubin,albumin,creatinine,Urea nitrogen
Time Frame
3 years
Title
Complications
Description
number of participants with Complications
Time Frame
3 years
Title
Times of interventional procedures
Description
The number of procedures for each patient, either TACE/TAE or ablation
Time Frame
3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jinhua Huang, Ph.D
Phone
0086-20-87343272
Email
huangjh@sysucc.org.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jinhua Huang, Ph.D
Organizational Affiliation
Sun Yat-sen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sun Yat-sen University Cancer Center
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510060
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jinhua Huang, Ph.D
Phone
0086-20-87343447
First Name & Middle Initial & Last Name & Degree
Jinhua Huang, Ph.D
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
RCT of TAE Simultaneously Combined Thermal Ablation for Large Hepatocellular Carcinoma
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