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TAE and MWA Combination Therapy in Early-stage Hepatocellular Carcinoma

Primary Purpose

Hepatocellular Carcinoma, Hepatoma, Liver Cancer, Adult

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Transarterial embolization
Microwave Ablation
Sponsored by
Wake Forest University Health Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatocellular Carcinoma focused on measuring Therapeutic Embolization, Ablation Techniques, Transarterial Embolization, TAE, Microwave Ablation, MWA

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Primary diagnosis of hepatocellular carcinoma (HCC)
  • HCC classification of stage 0 (very early) or stage A (early) according to Barcelona Clinic Liver Cancer (BCLC) staging system criteria
  • Adequate clinical condition to undergo laparoscopic or robot-assisted laparoscopic transarterial embolization (TAE) and/or microwave ablation (MWA) as treatment for HCC
  • Willing and able to give informed consent

Exclusion Criteria:

  • Radiologic (computed tomography or magnetic resonance imaging) evidence of invasion into major portal/hepatic venous branches and no extrahepatic metastases
  • Evidence of residual disease at first post-MWA computed tomography examination
  • Body Mass Index (BMI) > 35
  • Previous history of hepatic resections
  • Severe renal dysfunction (creatinine clearance of <40 mL/min)
  • Pregnant or nursing women

Sites / Locations

  • Carolinas Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

TAE + MWA combination therapy

MWA monotherapy

Arm Description

In patients randomized to receive the experimental therapy, transarterial embolization (TAE) treatments will be initiated within one week of randomization. Blunt embolization will be performed with LC beads with a maximum size of 700 µm. Microwave ablation (MWA) will be performed up to one month following randomization. The LC beads will be admixed with 8-15 mL of contrast and injected into the arterial branch at a rate of 1-2 mL/min. Treatment may be discontinued if any exclusion criteria develop in the patient or at the patient's request.

Microwave ablation (MWA) will be performed up to one month following randomization. Treatment may be discontinued if any exclusion criteria develop in the patient or at the patient's request. All operative MWAs will be performed in a laparoscopic or robot-assisted laparoscopic setting. All ablations will be guided by intraoperative ultrasound. Ablations will be performed with a 2.45-GHz generator with a 1.8-mm-diameter transcutaneous antenna.

Outcomes

Primary Outcome Measures

Intrahepatic Disease-free Survival
Defined as the absence of local or regional recurrence of hepatocellular carcinoma (HCC) as determined by diagnostic imaging

Secondary Outcome Measures

Overall Survival
Intrahepatic Disease-free Survival - 1 Year
Postoperative Morbidity
Postoperative Mortality
Overall Survival
Overall Survival - 3 Years
Overall Survival - 5 Year
Intrahepatic Disease-free Survival - 2 Year
Defined as the absence of local or regional recurrence of hepatocellular carcinoma (HCC) from date of treatment until 2 years after that date as determined by diagnostic imaging
Intrahepatic Disease-free Survival - 3 Year
Intrahepatic Disease-free Survival - 5 Year
Postoperative Morbidity

Full Information

First Posted
March 3, 2016
Last Updated
April 20, 2022
Sponsor
Wake Forest University Health Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT02704130
Brief Title
TAE and MWA Combination Therapy in Early-stage Hepatocellular Carcinoma
Official Title
Transarterial Embolization and Microwave Ablation Combination Therapy in Early-stage Hepatocellular Carcinoma: A Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Terminated
Why Stopped
Lack of funding
Study Start Date
March 2016 (Actual)
Primary Completion Date
January 2018 (Actual)
Study Completion Date
January 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Wake Forest University Health Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a single-center, prospective RCT to study the effectiveness of TACE and MWA combination therapy with MWA monotherapy for the treatment of early HCC. Primary outcome is 2-year intrahepatic disease-free survival.
Detailed Description
This single-center, prospective randomized controlled trial (RCT) is designed to compare the outcomes and clinicopathologic results of trans arterial embolization (TAE) and microwave ablation (MWA) combination therapy with MWA monotherapy for the treatment of early (stages 0 and A) hepatocellular carcinoma (HCC). The primary aim of this study is to test the following hypothesis: 2-year intrahepatic disease-free survival does not differ between patients receiving the experimental therapy (MWA + TAE) and patients receiving the standard therapy (MWA alone) as treatment for early stage HCC. Secondary aims are: 1) to determine the clinical feasibility of TAE + MWA in HCC patients with a small tumor burden using patient demographics and disease characteristic data and 2) to determine the effect of TAE on radiographic tumor characteristics in this patient cohort. The primary outcome is 2-year intrahepatic disease-free survival, which is measured from time of randomization and is defined as the absence of local or regional recurrence of HCC as determined by diagnostic imaging. Local recurrence is defined as an enhancing lesion contiguous with the ablation zone that is present on subsequent imaging but was not present on the initial post-ablation scan. Regional recurrence is defined as hepatic recurrence that is not adjacent to the ablation site.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma, Hepatoma, Liver Cancer, Adult, Liver Cell Carcinoma, Liver Cell Carcinoma, Adult
Keywords
Therapeutic Embolization, Ablation Techniques, Transarterial Embolization, TAE, Microwave Ablation, MWA

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
8 (Actual)

8. Arms, Groups, and Interventions

Arm Title
TAE + MWA combination therapy
Arm Type
Experimental
Arm Description
In patients randomized to receive the experimental therapy, transarterial embolization (TAE) treatments will be initiated within one week of randomization. Blunt embolization will be performed with LC beads with a maximum size of 700 µm. Microwave ablation (MWA) will be performed up to one month following randomization. The LC beads will be admixed with 8-15 mL of contrast and injected into the arterial branch at a rate of 1-2 mL/min. Treatment may be discontinued if any exclusion criteria develop in the patient or at the patient's request.
Arm Title
MWA monotherapy
Arm Type
Active Comparator
Arm Description
Microwave ablation (MWA) will be performed up to one month following randomization. Treatment may be discontinued if any exclusion criteria develop in the patient or at the patient's request. All operative MWAs will be performed in a laparoscopic or robot-assisted laparoscopic setting. All ablations will be guided by intraoperative ultrasound. Ablations will be performed with a 2.45-GHz generator with a 1.8-mm-diameter transcutaneous antenna.
Intervention Type
Device
Intervention Name(s)
Transarterial embolization
Other Intervention Name(s)
TAE
Intervention Description
In transarterial bland embolization, beads are delivered directly into the arterial vessels feeding the tumor, usually by a percutaneous coaxial catheter system guided by ultrasound or fluoroscopy through the common femoral artery.
Intervention Type
Procedure
Intervention Name(s)
Microwave Ablation
Intervention Description
Microwave ablation is a form of thermal ablation used to treat cancer. In this procedure, electromagnetic waves in the microwave energy spectrum (300 MHz to 300 GHz) are applied to tumor tissue. The oscillation of polar molecules produces frictional heating, ultimately generating tissue necrosis within solid tumors.
Primary Outcome Measure Information:
Title
Intrahepatic Disease-free Survival
Description
Defined as the absence of local or regional recurrence of hepatocellular carcinoma (HCC) as determined by diagnostic imaging
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Overall Survival
Time Frame
1 year
Title
Intrahepatic Disease-free Survival - 1 Year
Time Frame
1 year
Title
Postoperative Morbidity
Time Frame
1 month
Title
Postoperative Mortality
Time Frame
Assessed at 1 month and 3 months, total number up to 3 months reported
Title
Overall Survival
Time Frame
2 Years
Title
Overall Survival - 3 Years
Time Frame
3 Years
Title
Overall Survival - 5 Year
Time Frame
5 Years
Title
Intrahepatic Disease-free Survival - 2 Year
Description
Defined as the absence of local or regional recurrence of hepatocellular carcinoma (HCC) from date of treatment until 2 years after that date as determined by diagnostic imaging
Time Frame
2 Year
Title
Intrahepatic Disease-free Survival - 3 Year
Time Frame
3 Year
Title
Intrahepatic Disease-free Survival - 5 Year
Time Frame
5 Year
Title
Postoperative Morbidity
Time Frame
3 Month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Primary diagnosis of hepatocellular carcinoma (HCC) HCC classification of stage 0 (very early) or stage A (early) according to Barcelona Clinic Liver Cancer (BCLC) staging system criteria Adequate clinical condition to undergo laparoscopic or robot-assisted laparoscopic transarterial embolization (TAE) and/or microwave ablation (MWA) as treatment for HCC Willing and able to give informed consent Exclusion Criteria: Radiologic (computed tomography or magnetic resonance imaging) evidence of invasion into major portal/hepatic venous branches and no extrahepatic metastases Evidence of residual disease at first post-MWA computed tomography examination Body Mass Index (BMI) > 35 Previous history of hepatic resections Severe renal dysfunction (creatinine clearance of <40 mL/min) Pregnant or nursing women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dionisios Vrochides, MD PhD
Organizational Affiliation
Carolinas Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Carolinas Medical Center
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
28204
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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TAE and MWA Combination Therapy in Early-stage Hepatocellular Carcinoma

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