Adjuvant Therapies for Patients With HCC and MVI (A-TACE/S-HCC)
Primary Purpose
Hepatocellular Carcinoma
Status
Unknown status
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
TACE
Sorafenib
TACE plus sorafenib
empty control
Sponsored by

About this trial
This is an interventional treatment trial for Hepatocellular Carcinoma
Eligibility Criteria
Inclusion Criteria:
- Age 18-75 years
- Diagnosis of HCC was confirmed by histopathological examination of surgical samples in all patients
- Patients with microvascular invasion by histopathological examination of surgical samples
- Patients have Child-Pugh A or B liver function
- No previous neoadjuvant treatment
- No evidence of macrovascular invasion, metastasis to the lymph nodes and/or distant metastases on the basis of preoperative imaging results and perioperative findings
- No malignancy other than HCC for 5 years prior to the initial HCC treatment
Exclusion Criteria:
- History of cardiac disease
- Known history of human immunodeficiency virus (HIV) infection
- Known Central Nervous System tumors including metastatic brain disease
- History of organ allograft
- Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of the study results
- Any condition that is unstable or which could jeopardize the safety of the patient and his/her compliance in the study
- Pregnant or breast-feeding patients
Sites / Locations
- Department of Hepatobilliary Surgery, Affiliated Tumor of Guangxi UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Active Comparator
Other
No Intervention
Arm Label
TACE
sorafenib
TACE plus sorafenib
empty control
Arm Description
Transarterial chemoembolization (TACE) is performed two to four weeks after hepatic resection.
Patients will receive sorafenib at a dose of 400 mg twice daily after 2 weeks of hepatic resection.
Patients will receive sorafenib at a dose of 400 mg twice daily after 2 weeks of hepatic resection. At the same time, TACE is performed two to four weeks after hepatic resection.
This group patients will receive best supportive care.
Outcomes
Primary Outcome Measures
Overall survivals
Secondary Outcome Measures
Hospital mortality
Recurrence rates
Full Information
NCT ID
NCT02436902
First Posted
April 28, 2015
Last Updated
January 7, 2020
Sponsor
Guangxi Medical University
1. Study Identification
Unique Protocol Identification Number
NCT02436902
Brief Title
Adjuvant Therapies for Patients With HCC and MVI
Acronym
A-TACE/S-HCC
Official Title
Adjuvant Transarterial Chemoembolization With or Without Sorafenib for Patients With Hepatocellular Carcinoma and Microvascular Invasion
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
February 1, 2019 (Actual)
Primary Completion Date
August 23, 2022 (Anticipated)
Study Completion Date
August 30, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Guangxi Medical University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Hepatocellular carcinoma (HCC) is a common malignancy, and its incidence is expected to increase in many countries in coming decades. Though prognosis for patients with HCC is generally poor, hepatic resection can be an effective curative treatment, and its indications have been expanding in recent years. Resection can be reasonably safe and effective even for patients with micro- or macrovascular invasion. However, the recurrence rate of HCC is as high as 74% for patients with intermediate and advanced HCC after resection. Microvascular invasion is one of the main risk factors which influence risk of HCC recurrence and patient prognosis after resection. Therefore, adjuvant therapy to prevent tumor recurrence after resection is so important to improve patient prognosis.
Nowadays, adjuvant transarterial chemoembolization (TACE) is reported to be effective in reducing early recurrence rate and mortality for patients with HCC with risk factors of recurrence. Sorafenib is a novel drug which is effective for advanced stage HCC. However, the efficacy of adjuvant sorafenib for postoperative HCC is unknown. Therefore, it is interesting to investigate the efficacy of adjuvant sorafenib, and compare its efficacy to TACE, TACE plus sorafenib, or best supportive care for patients with postoperative HCC and microvascular invasion.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
240 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
TACE
Arm Type
Experimental
Arm Description
Transarterial chemoembolization (TACE) is performed two to four weeks after hepatic resection.
Arm Title
sorafenib
Arm Type
Active Comparator
Arm Description
Patients will receive sorafenib at a dose of 400 mg twice daily after 2 weeks of hepatic resection.
Arm Title
TACE plus sorafenib
Arm Type
Other
Arm Description
Patients will receive sorafenib at a dose of 400 mg twice daily after 2 weeks of hepatic resection. At the same time, TACE is performed two to four weeks after hepatic resection.
Arm Title
empty control
Arm Type
No Intervention
Arm Description
This group patients will receive best supportive care.
Intervention Type
Procedure
Intervention Name(s)
TACE
Other Intervention Name(s)
transarterial chemoembolization
Intervention Description
TACE is performed one month after resection.
Intervention Type
Drug
Intervention Name(s)
Sorafenib
Intervention Description
Sorafenib is submitted one month after resection.
Intervention Type
Drug
Intervention Name(s)
TACE plus sorafenib
Intervention Description
TACE plus sorafenib will be submitted one month after resection.
Intervention Type
Other
Intervention Name(s)
empty control
Intervention Description
This group will not receive adjuvant therapy.
Primary Outcome Measure Information:
Title
Overall survivals
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Hospital mortality
Time Frame
30-day
Title
Recurrence rates
Time Frame
1 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Age 18-75 years
Diagnosis of HCC was confirmed by histopathological examination of surgical samples in all patients
Patients with microvascular invasion by histopathological examination of surgical samples
Patients have Child-Pugh A or B liver function
No previous neoadjuvant treatment
No evidence of macrovascular invasion, metastasis to the lymph nodes and/or distant metastases on the basis of preoperative imaging results and perioperative findings
No malignancy other than HCC for 5 years prior to the initial HCC treatment
Exclusion Criteria:
History of cardiac disease
Known history of human immunodeficiency virus (HIV) infection
Known Central Nervous System tumors including metastatic brain disease
History of organ allograft
Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of the study results
Any condition that is unstable or which could jeopardize the safety of the patient and his/her compliance in the study
Pregnant or breast-feeding patients
Facility Information:
Facility Name
Department of Hepatobilliary Surgery, Affiliated Tumor of Guangxi University
City
Nanning
State/Province
Guangxi
ZIP/Postal Code
530021
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bang-De Xiang, MD,PhD
Phone
86-771-5330855
Email
xiangbangde@163.com
12. IPD Sharing Statement
Citations:
PubMed Identifier
20887328
Citation
Zhong JH, Li LQ. Postoperative adjuvant transarterial chemoembolization for participants with hepatocellular carcinoma: A meta-analysis. Hepatol Res. 2010 Oct;40(10):943-53. doi: 10.1111/j.1872-034X.2010.00710.x.
Results Reference
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PubMed Identifier
18650514
Citation
Llovet JM, Ricci S, Mazzaferro V, Hilgard P, Gane E, Blanc JF, de Oliveira AC, Santoro A, Raoul JL, Forner A, Schwartz M, Porta C, Zeuzem S, Bolondi L, Greten TF, Galle PR, Seitz JF, Borbath I, Haussinger D, Giannaris T, Shan M, Moscovici M, Voliotis D, Bruix J; SHARP Investigators Study Group. Sorafenib in advanced hepatocellular carcinoma. N Engl J Med. 2008 Jul 24;359(4):378-90. doi: 10.1056/NEJMoa0708857.
Results Reference
background
PubMed Identifier
25713907
Citation
Zhou L, Rui JA, Wang SB, Chen SG, Qu Q. Early recurrence in large hepatocellular carcinoma after curative hepatic resection: prognostic significance and risk factors. Hepatogastroenterology. 2014 Oct;61(135):2035-41.
Results Reference
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Adjuvant Therapies for Patients With HCC and MVI
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