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Combine TACE and RFA Versus RFA Monotherapy in Unilobar HCC of 3.1 to 7 cm Patient

Primary Purpose

Hepatocellular Carcinoma

Status
Unknown status
Phase
Phase 2
Locations
Taiwan
Study Type
Interventional
Intervention
Transcatheter Arterial Chemoembolization
Radiofrequency ablation
Doxorubicin
Sponsored by
Shi-Ming Lin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatocellular Carcinoma focused on measuring HCC, hepatocellular carcinoma, liver cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age >18 years;
  • Unresectable HCC or patients with resectable HCC but not appropriate for resection;.
  • Tumor stage: single tumor with 3.1-7cm in diameter, or multiple (maximum 3) tumors with at least one over 3cm but only one of the multiple tumors larger than 5cm for concerning too prolonged time of RFA. All the target tumors are located in single lobe.
  • The lesion should be detected on ultrasonography;
  • The divergence of the hepatic artery was suitable for TACE;
  • Absence of portal and venous thrombosis, extrahepatic metastases, or uncontrollable ascites;
  • Patients in Child-Pugh grade A or B;
  • Eastern Cooperative Oncology Group performance status score of 2 or less;
  • Patient has signed consent form regarding participation in the study.

Exclusion Criteria:

  • Patients had previously received any treatment for HCC;
  • Patients with known renal or cardiovascular disease before TACE;
  • Child-Pugh grade C cirrhosis, prior decompensation and history of encephalopathy before TACE
  • Pregnancy or plan to pregnant in the subsequent study period (1 to 2 years)

Sites / Locations

  • Chang Gung Memorial Hospital, Lin-KuoRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

TACE+ RFA

RFA

Arm Description

This arm will be conventional TACE(Transcatheter Arterial Chemoembolization) plus RFA(radiofrequency ablation. use intra-injection of lipiodol mized with doxorubicin when the catheter was placed in the superselective location very close to the tumor.

Recent advances in local ablation are aimed to expand the ablation size (> 3cm in diameter) in a minimal session by utilizing the switching RF controller and simultaneous 2 or 3 RF electrodes placement. The procedure of RFA was according to manufacture algorithm. RFA was performed within 7 days after TACE because the embolization effect in reducing blood flow will be not evident afterwards.

Outcomes

Primary Outcome Measures

The rate of complete necrosis (CN)
The complete necrosis (or complete coagulation, complete necrosis, complete response) that is defined as persistent hypo-attenuation of the tumor on triphasic dynamic CT scan or MRI one month after the last ablation therapy. When no enhancing lesion was seen on CT after the initial ablation, primary technique effectiveness was considered to have been achieved. When lesion enhancement was still seen on CT, primary technique effectiveness was not considered as achieved. A course of treatment for each tumour was limited to three RF ablation sessions within 3 months

Secondary Outcome Measures

Primary technique effectiveness
i.e. achievement of complete necrosis after maximum of 3 treatment sessions. When no enhancing lesion was seen on CT after the initial ablation, primary technique effectiveness was considered to have been achieved. When lesion enhancement was still seen on CT, primary technique effectiveness was not considered as achieved. A course of treatment for each tumour was limited to three RF ablation sessions within 3 months.
local tumor progression of HCC
this was defined as the appearance of nodular enhancement contiguous with the ablated tumor on dynamic imaging or an increase in the size of the ablated area on follow-up imaging of a tumor that was previously completely ablated.
Survival
That was determined from the date of RF ablation to that of last follow-up or death.
Major complication
that was defined as those requiring treatment with hospitalization or involving permanent adverse sequelae.

Full Information

First Posted
May 11, 2013
Last Updated
May 22, 2013
Sponsor
Shi-Ming Lin
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1. Study Identification

Unique Protocol Identification Number
NCT01858207
Brief Title
Combine TACE and RFA Versus RFA Monotherapy in Unilobar HCC of 3.1 to 7 cm Patient
Official Title
Combine Chemoembolization and Radiofrequency Ablation Versus Radiofrequency Ablation Monotherapy for Patients With Unilobar Hepatocellular Carcinoma of 3.1 to 7 cm: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2013
Overall Recruitment Status
Unknown status
Study Start Date
January 2012 (undefined)
Primary Completion Date
July 2014 (Anticipated)
Study Completion Date
December 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Shi-Ming Lin

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Abstract of Research Proposal Radiofrequency ablation (RFA) has been proved to be a curative treatment with minimal invasiveness and high efficacy for small hepatocellular carcinoma (HCC) that is generally defined as maximal diameter no larger than 3cm. RFA can achieve a rate of complete necrosis as 80-100% in small HCC. However, the rate will drop to 71% in HCC of 3.1-5cm and 25% for HCC larger than 5cm。This is due to the relative hypervascularity for the bigger tumor and it will induce heat sink that leading to less effect of ablation. Therefore, transcatheter chemoembolization (TACE) before RFA may reduce the vascularity and enhance the effect of subsequent RFA. Moreover, pre-RF TACE will reduce the tumor size and the subsequent RFA will be more effective than RFA alone. In retrospective studies, Kitamoto M et al showed that tumor necrosis diameter was larger in TACE and RFA combination therapies compared to RFA mono-therapy; Yamakado K et al showed that TACE and RFA combination therapies in HCC (maximal diameter up to 12 cm) achieved 100% complete necrosis, 0% local recurrence rate and 93% of 2-year survival rate. Nevertheless, only one randomized trial in intermediate size HCC (3-5cm in diameter) showed that TACE and RFA combination therapies achieved a significant higher rate of complete necrosis, technique success, fewer treatment sessions to achieve complete necrosis and lower local recurrence but non-significant difference in 3-year survival rate. Therefore, based on the limited studies, combine TACE and RFA may achieve better effects than RFA mono-therapy in HCC larger than 3cm. However, repeat TACE may induce some complications such as HBV reactivation, hepatitis or even liver decompensation. Moreover, novel RFA using simultaneous multiple RFA probes with switching RF controller may achieve a better effects and shorter ablation time than sequential RFA with single electrode. Thus, is it still necessary using TACE and RFA combination therapies for HCC >3cm when application of novel switching RF controller? The aim of the current study is to conduct a RCT comparing combine TACE and RFA compared to RFA mono-therapy by using simultaneous multiple electrodes and switching RF controller in uni-lobar HCC of 3.1-7cm. The rate of complete necrosis, technique success, sessions to achieve CN, local tumor progression, survival rate and major complications will be analyzed. Investigators cannot expect which one is better, safer before the achievement of the study.
Detailed Description
Specific Aims: The aim of the current study is to compare TACE and RFA combination therapies with RFA mono-therapy by using simultaneous multiple electrodes and switching RF controller in the treatment of uni-lobar HCC of 3.1 to 7cm. The rate of complete necrosis (CN), technique success, sessions to achieve CN, local tumor progression, survival rate and major complications will be analyzed. Background: HCC is 4th mostly common malignancy worldwide and the leading cause of cancer-death in Taiwan. Surveillance programs can detect HCC at early stage. Surgical resection, liver transplantation and local ablation are currently considered as curative treatment modalities for early stage HCC. However, only 10-30% of early stage HCC is suitable for resection due to poor liver reserve, co-morbidity and shortage of liver donor. Therefore, local ablation plays an important role in the treatment of unresectable or resectable early-stage HCC. Among the various local ablative modalities, radiofrequency ablation (RFA) has been proved to be a curative treatment with minimal invasiveness and high efficacy for small HCC that is generally defined as maximal diameter no larger than 3cm. RFA can achieve a rate of complete necrosis as 80-100% in small HCC. However, the rate will drop to 71% in HCC of 3.1-5cm and 25% for HCC > 5cm。 The difference is due to the relative hypervascularity for the bigger tumor and it will induce heat sink that leading to less effect of ablation. Therefore, transcatheter chemoembolization (TACE) before RFA may reduce the vascularity and enhance the effect of subsequent RFA. Moreover, pre-RF TACE will reduce the tumor size and the subsequent RFA to unembolized viable tumor will be more effective than RFA alone. In retrospective studies, Kitamoto M et al showed that tumor necrosis diameter was larger in combine TACE and RFA compared to RFA monotherapy; Yamakado K et al showed that combine TACE and RFA in HCC (maximal diameter up to 12 cm) achieved 100% complete necrosis, 0% local recurrence rate and 93% of 2-year survival rate. Nevertheless, only one randomized trial in intermediate size HCC (3-5cm in diameter) showed that combine TACE and RFA achieved a significant higher rate of technique success, fewer treatment sessions and lower local recurrence but non-significant in 3-year survival rate. Therefore, based on the limited studies, combine TACE and RFA may achieve better effects than RFA mono-therapy in HCC larger than 3cm. However, repeat TACE may induce some complications such as HBV reactivation, hepatitis or even liver decompensation. Moreover, novel RFA using simultaneous multiple RFA probes with switching RF controller may achieve a better effects and shorter ablation time than sequential RFA with single electrode. Thus, is it still necessary using TACE and RFA combination therapies for HCC > 3cm when application of novel switching RF controller? aim of the current study is to conduct a RCT comparing combine TACE and RFA compared to RFA mono-therapy by using simultaneous multiple electrodes and switching RF controller in uni-lobar HCC of 3.1-7cm. The rate of complete necrosis, sessions to achieve CN, primary technique effectiveness (i.e. achievement of complete necrosis after maximum of 3 treatment sessions), local tumor progression, survival rate and major complications will be analyzed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma
Keywords
HCC, hepatocellular carcinoma, liver cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
TACE+ RFA
Arm Type
Active Comparator
Arm Description
This arm will be conventional TACE(Transcatheter Arterial Chemoembolization) plus RFA(radiofrequency ablation. use intra-injection of lipiodol mized with doxorubicin when the catheter was placed in the superselective location very close to the tumor.
Arm Title
RFA
Arm Type
Active Comparator
Arm Description
Recent advances in local ablation are aimed to expand the ablation size (> 3cm in diameter) in a minimal session by utilizing the switching RF controller and simultaneous 2 or 3 RF electrodes placement. The procedure of RFA was according to manufacture algorithm. RFA was performed within 7 days after TACE because the embolization effect in reducing blood flow will be not evident afterwards.
Intervention Type
Procedure
Intervention Name(s)
Transcatheter Arterial Chemoembolization
Other Intervention Name(s)
TACE, Chemoembolization
Intervention Description
traditional TACE, conventional TACE
Intervention Type
Procedure
Intervention Name(s)
Radiofrequency ablation
Other Intervention Name(s)
RFA
Intervention Description
simultaneous multiple electrodes and switching RF controller
Intervention Type
Drug
Intervention Name(s)
Doxorubicin
Intervention Description
TACE will be done according to the current method in our center. We use intra-injection of lipiodol mized with doxorubicin when the catheter was placed in the superselective location very close to the tumor. Gelfoam sponge was then injected to temporarily occlude the arterial blood flow.
Primary Outcome Measure Information:
Title
The rate of complete necrosis (CN)
Description
The complete necrosis (or complete coagulation, complete necrosis, complete response) that is defined as persistent hypo-attenuation of the tumor on triphasic dynamic CT scan or MRI one month after the last ablation therapy. When no enhancing lesion was seen on CT after the initial ablation, primary technique effectiveness was considered to have been achieved. When lesion enhancement was still seen on CT, primary technique effectiveness was not considered as achieved. A course of treatment for each tumour was limited to three RF ablation sessions within 3 months
Time Frame
2014 Dec (up to 3 years)
Secondary Outcome Measure Information:
Title
Primary technique effectiveness
Description
i.e. achievement of complete necrosis after maximum of 3 treatment sessions. When no enhancing lesion was seen on CT after the initial ablation, primary technique effectiveness was considered to have been achieved. When lesion enhancement was still seen on CT, primary technique effectiveness was not considered as achieved. A course of treatment for each tumour was limited to three RF ablation sessions within 3 months.
Time Frame
2014 Dec (up to 3 years)
Title
local tumor progression of HCC
Description
this was defined as the appearance of nodular enhancement contiguous with the ablated tumor on dynamic imaging or an increase in the size of the ablated area on follow-up imaging of a tumor that was previously completely ablated.
Time Frame
2014 Dec (up to 3 years)
Title
Survival
Description
That was determined from the date of RF ablation to that of last follow-up or death.
Time Frame
2014 dec (up to 3 years)
Title
Major complication
Description
that was defined as those requiring treatment with hospitalization or involving permanent adverse sequelae.
Time Frame
2014 Dec (up to 3 years)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age >18 years; Unresectable HCC or patients with resectable HCC but not appropriate for resection;. Tumor stage: single tumor with 3.1-7cm in diameter, or multiple (maximum 3) tumors with at least one over 3cm but only one of the multiple tumors larger than 5cm for concerning too prolonged time of RFA. All the target tumors are located in single lobe. The lesion should be detected on ultrasonography; The divergence of the hepatic artery was suitable for TACE; Absence of portal and venous thrombosis, extrahepatic metastases, or uncontrollable ascites; Patients in Child-Pugh grade A or B; Eastern Cooperative Oncology Group performance status score of 2 or less; Patient has signed consent form regarding participation in the study. Exclusion Criteria: Patients had previously received any treatment for HCC; Patients with known renal or cardiovascular disease before TACE; Child-Pugh grade C cirrhosis, prior decompensation and history of encephalopathy before TACE Pregnancy or plan to pregnant in the subsequent study period (1 to 2 years)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shi-Ming Lin, MD.
Phone
886-3-3281200
Ext
8107
Email
lsmpaicyto@cgmh.org.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shi-Ming Lin, MD
Organizational Affiliation
Chang Gung Medical Foundation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chang Gung Memorial Hospital, Lin-Kuo
City
Taoyuan
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yu-Ray Chen
Phone
+886-2-27135211
First Name & Middle Initial & Last Name & Degree
Shih-Ming Lin, MD.
First Name & Middle Initial & Last Name & Degree
Chen-Chun Lin, MD.
First Name & Middle Initial & Last Name & Degree
Kar-Wai Lu, MD

12. IPD Sharing Statement

Learn more about this trial

Combine TACE and RFA Versus RFA Monotherapy in Unilobar HCC of 3.1 to 7 cm Patient

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