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Drug-eluting Bead Transarterial Chemoembolisation (DEB-TACE) Versus (VS) Conventional Transarterial Chemoembolisation (cTACE) for Unresectable Hepatocellualr Carcinoma (HCC)

Primary Purpose

Hepatocellular Carcinoma

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
DEB-TACE
cTACE
Sponsored by
Air Force Military Medical University, China
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatocellular Carcinoma focused on measuring Hepatocellular Carcinoma, Drug-eluting bead transarterial chemoembolization, Conventional transarterial chemoembolization, Objective response

Eligibility Criteria

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

Inclusion Criteria:

  1. Prior informed consent
  2. Confirmed Diagnosis of HCC: a. Cirrhotic subjects: Clinical diagnosis by American Association for the Study of Liver Diseases (AASLD) criteria. HCC can be defined in cirrhotic subjects by one imaging technique (CT scan, MRI, or second generation contrast ultrasound) showing a nodule larger than 2 cm with contrast uptake in the arterial phase and washout in venous or late phases or two imaging techniques showing this radiological behavior for nodules of 1-2 cm in diameter. Cytohistological confirmation is required for subjects who do not fulfill these eligibility criteria. b. Non-cirrhotic subjects: For subjects without cirrhosis, histological or cytological confirmation is mandatory. Documentation of original biopsy for diagnosis is acceptable
  3. Patients with unresectable Barcelona Clinic Liver Cancer (BCLC) stage A and BCLC B, and all patients have a intermediate or high tumor burden (the diameter of largest tumor plus tumor number is more than 6)
  4. Child Pugh class A/B(7) class without decompensated liver cirrhosis.
  5. ECOG Performance Status 0 score
  6. At least one uni-dimensional lesion measurable by MRI or CT according to the RECIST 1.1 criteria
  7. Male or female subject larger than 18 years of age
  8. Life expectance of at least 12 weeks.
  9. Both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial and 4 weeks after the completion of trial
  10. Adequate bone marrow, liver and renal function as assessed by central lab by means of the following laboratory requirements from samples within 7 days prior to randomization:

    1. Hemoglobin > 9.0 g/dl
    2. Absolute neutrophil count (ANC) >1,500/mm3
    3. Platelet count≥50x109/L
    4. ALB≥28g/L
    5. Total bilirubin < 2 mg/dL
    6. Alanine aminotransferase(ALT) and aspartate aminotransferase(AST) < 5 x upper limit of normal
    7. Blood urea nitrogen(BUN) and creatinine < 1.5 x upper limit of normal
    8. International normalized ratio(INR) < 1.7, or prothrombin time(PT) < 4 seconds above control

Exclusion Criteria:

  1. Portal vein or any vascular invasion
  2. Presence of extra hepatic spread
  3. Presence of metastasis in biliary tract or obstruction of biliary tract
  4. Presence of metastasis in brain or presence of symptom of the brain metastasis but lack of further examination to exclude brain metastasis
  5. Poor blood supply for the liver tumor lesions; poor blood supply refers that the tumor lesions fail to show obvious contrast uptake in the arterial phase and washout in venous or late phases by CT scan or MRI
  6. Any contraindications for hepatic embolization procedures:

    1. Known hepatofugal blood flow
    2. Known porto-systemic shunt
    3. Renal failure / insufficiency requiring hemo-or peritoneal dialysis
  7. History of cardiac disease:

    1. Congestive heart failure >New York Heart Association (NYHA) class 2
    2. Uncontrolled hypertension
  8. Known history of HIV infection
  9. Patients who have previously been receiving any treatments against HCC
  10. Active clinically serious infections (> grade 2 NCI-CTCAE Version 4.0), except for hepatitis B virus (HBV) and hepatitis C virus (HCV) infection
  11. Contraindication of Anthracyclines administration, such as Doxorubicin
  12. Concurrent with other cancer
  13. Pregnant or breast-feeding subjects
  14. Women of childbearing age did not take any contraceptive measures
  15. Clinically significant gastrointestinal bleeding within 12 weeks prior to start of study
  16. Major surgery within 3 weeks prior to start of study drug (e.g. thoracolaparotomy is not allowed, but noninvasive surgery, e.g. biopsy, is allowed)

Sites / Locations

  • Xijing Hospital of Digestive Diseases, Fourth Military Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

DEB-TACE

cTACE

Arm Description

172 subjects in this study group will be receive the treatment of drug-eluting bead TACE

172 subjects in this study group will be receive the treatment of conventional TACE

Outcomes

Primary Outcome Measures

Objective response rate
the percentage of patients who achieved complete response (CR) and partial response (PR) as the best response, according to the modified Response Evaluation Criteria In Solid Tumours (mRECIST) criteria

Secondary Outcome Measures

Overall survival
Overall survival (OS) is measured from the treatment start until all-cause death or the last follow-up date
Time to progression
Time to progression is measured from the treatment start to the radiologically confirmed progression
Adverse event
The terms and grade of adverse event will be present according to the Common Terminology Criteria for Adverse Event (CTCAE version 4.0)
Progression-free survival
Progression-free survival (PFS) is measured from the treatment start until all-cause death or untreatable progression (vascular invasion, extra hepatic spread, the Eastern Cooperative Oncology Group (ECOG) performance status >2, and Child-Pugh grade over C, but except hepatic new nodule)
Time to response
Time to response (TTR) is measured from the treatment start to the firstly radiologically confirmed complete response or partial response.
Duration of response
Duration of response (DOR) is measured from the first-time confirmed complete response or partial response to the date of radiological progression

Full Information

First Posted
May 29, 2019
Last Updated
February 4, 2020
Sponsor
Air Force Military Medical University, China
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1. Study Identification

Unique Protocol Identification Number
NCT03969576
Brief Title
Drug-eluting Bead Transarterial Chemoembolisation (DEB-TACE) Versus (VS) Conventional Transarterial Chemoembolisation (cTACE) for Unresectable Hepatocellualr Carcinoma (HCC)
Official Title
Efficacy and Safety of Drug-eluting Bead TACE VS Conventional TACE for Unresectable Hepatocellular Carcinoma: a Multicenter, Prospective Cohort Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
September 15, 2020 (Anticipated)
Primary Completion Date
June 15, 2022 (Anticipated)
Study Completion Date
June 15, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Air Force Military Medical University, China

4. Oversight

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

5. Study Description

Brief Summary
this multi-center prospective cohort study is to evaluate the efficacy and the safety of drug-eluting bead TACE compared with conventional TACE in terms of objective response in unresectable HCC

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma
Keywords
Hepatocellular Carcinoma, Drug-eluting bead transarterial chemoembolization, Conventional transarterial chemoembolization, Objective response

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Non-Randomized
Enrollment
344 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
DEB-TACE
Arm Type
Experimental
Arm Description
172 subjects in this study group will be receive the treatment of drug-eluting bead TACE
Arm Title
cTACE
Arm Type
Active Comparator
Arm Description
172 subjects in this study group will be receive the treatment of conventional TACE
Intervention Type
Procedure
Intervention Name(s)
DEB-TACE
Other Intervention Name(s)
drug-eluting bead transarterial chemoembolisation
Intervention Description
Patients in the DEB-TACE group received a maximum dose of 4 ml of DC bead (diameter 75-500 um) loaded with a maximum dose of 150 mg of anthracyclines drugs, such as doxorubicin. The anticancer agents and the diameter of DC Bead for individual patient will be selected according to the common clinical practice of each center. Treatment endpoint consisted of stasis of flow within feeding vessel(s) or completed delivery of maximum single-session dose of 150 mg doxorubicin. TACE will be repeated "on demand" according to the radiological response.
Intervention Type
Procedure
Intervention Name(s)
cTACE
Other Intervention Name(s)
conventional transarterial chemoembolisation
Intervention Description
Patients in the cTACE group were treated with anthracyclines, such as doxorubicin, in a mixture of lipiodol. Administration of the anticancer in oil emulsion was followed by injection of embolic materials such as gelfoam or PVA particles until complete stasis in segmental or subsegmental arterial branches. the tumor-feeding vessels should be superselected whenever possible. The anticancer agents for individual patient will be selected according to the common clinical practice of each center. TACE will be repeated "on demand" according to the radiological response.
Primary Outcome Measure Information:
Title
Objective response rate
Description
the percentage of patients who achieved complete response (CR) and partial response (PR) as the best response, according to the modified Response Evaluation Criteria In Solid Tumours (mRECIST) criteria
Time Frame
Tumor response will be assessed at week 4 and week 12 after initiation of treatment and thereafter every 8 weeks, up to 1 year
Secondary Outcome Measure Information:
Title
Overall survival
Description
Overall survival (OS) is measured from the treatment start until all-cause death or the last follow-up date
Time Frame
The last patient has been on study for 1year
Title
Time to progression
Description
Time to progression is measured from the treatment start to the radiologically confirmed progression
Time Frame
The last patient has been on study for 1year
Title
Adverse event
Description
The terms and grade of adverse event will be present according to the Common Terminology Criteria for Adverse Event (CTCAE version 4.0)
Time Frame
The adverse event will be assessed during in hospital and every 4 weeks, up to 1year
Title
Progression-free survival
Description
Progression-free survival (PFS) is measured from the treatment start until all-cause death or untreatable progression (vascular invasion, extra hepatic spread, the Eastern Cooperative Oncology Group (ECOG) performance status >2, and Child-Pugh grade over C, but except hepatic new nodule)
Time Frame
The last patient has been on study for 1year
Title
Time to response
Description
Time to response (TTR) is measured from the treatment start to the firstly radiologically confirmed complete response or partial response.
Time Frame
The last patient has been on study for 1year
Title
Duration of response
Description
Duration of response (DOR) is measured from the first-time confirmed complete response or partial response to the date of radiological progression
Time Frame
The last patient has been on study for 1year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Prior informed consent Confirmed Diagnosis of HCC: a. Cirrhotic subjects: Clinical diagnosis by American Association for the Study of Liver Diseases (AASLD) criteria. HCC can be defined in cirrhotic subjects by one imaging technique (CT scan, MRI, or second generation contrast ultrasound) showing a nodule larger than 2 cm with contrast uptake in the arterial phase and washout in venous or late phases or two imaging techniques showing this radiological behavior for nodules of 1-2 cm in diameter. Cytohistological confirmation is required for subjects who do not fulfill these eligibility criteria. b. Non-cirrhotic subjects: For subjects without cirrhosis, histological or cytological confirmation is mandatory. Documentation of original biopsy for diagnosis is acceptable Patients with unresectable Barcelona Clinic Liver Cancer (BCLC) stage A and BCLC B, and all patients have a intermediate or high tumor burden (the diameter of largest tumor plus tumor number is more than 6) Child Pugh class A/B(7) class without decompensated liver cirrhosis. ECOG Performance Status 0 score At least one uni-dimensional lesion measurable by MRI or CT according to the RECIST 1.1 criteria Male or female subject larger than 18 years of age Life expectance of at least 12 weeks. Both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial and 4 weeks after the completion of trial Adequate bone marrow, liver and renal function as assessed by central lab by means of the following laboratory requirements from samples within 7 days prior to randomization: Hemoglobin > 9.0 g/dl Absolute neutrophil count (ANC) >1,500/mm3 Platelet count≥50x109/L ALB≥28g/L Total bilirubin < 2 mg/dL Alanine aminotransferase(ALT) and aspartate aminotransferase(AST) < 5 x upper limit of normal Blood urea nitrogen(BUN) and creatinine < 1.5 x upper limit of normal International normalized ratio(INR) < 1.7, or prothrombin time(PT) < 4 seconds above control Exclusion Criteria: Portal vein or any vascular invasion Presence of extra hepatic spread Presence of metastasis in biliary tract or obstruction of biliary tract Presence of metastasis in brain or presence of symptom of the brain metastasis but lack of further examination to exclude brain metastasis Poor blood supply for the liver tumor lesions; poor blood supply refers that the tumor lesions fail to show obvious contrast uptake in the arterial phase and washout in venous or late phases by CT scan or MRI Any contraindications for hepatic embolization procedures: Known hepatofugal blood flow Known porto-systemic shunt Renal failure / insufficiency requiring hemo-or peritoneal dialysis History of cardiac disease: Congestive heart failure >New York Heart Association (NYHA) class 2 Uncontrolled hypertension Known history of HIV infection Patients who have previously been receiving any treatments against HCC Active clinically serious infections (> grade 2 NCI-CTCAE Version 4.0), except for hepatitis B virus (HBV) and hepatitis C virus (HCV) infection Contraindication of Anthracyclines administration, such as Doxorubicin Concurrent with other cancer Pregnant or breast-feeding subjects Women of childbearing age did not take any contraceptive measures Clinically significant gastrointestinal bleeding within 12 weeks prior to start of study Major surgery within 3 weeks prior to start of study drug (e.g. thoracolaparotomy is not allowed, but noninvasive surgery, e.g. biopsy, is allowed)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Guohong Han, MD PHD
Phone
+86-2984771528
Email
hangh@fmmu.edu.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Dongdong Xia, MD
Phone
+86-2984771528
Email
xiadongdong1026@163.com
Facility Information:
Facility Name
Xijing Hospital of Digestive Diseases, Fourth Military Medical University
City
Xi'an
State/Province
Shaanxi
ZIP/Postal Code
710032
Country
China

12. IPD Sharing Statement

Learn more about this trial

Drug-eluting Bead Transarterial Chemoembolisation (DEB-TACE) Versus (VS) Conventional Transarterial Chemoembolisation (cTACE) for Unresectable Hepatocellualr Carcinoma (HCC)

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