Adjuvant Therapy With Thalidomide After Curative Resection of Hepatocellular Carcinoma
Primary Purpose
Hepatocellular Carcinoma, Recurrence
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Thalidomide
Sponsored by
About this trial
This is an interventional prevention trial for Hepatocellular Carcinoma
Eligibility Criteria
Inclusion Criteria:
- 18-75 years old,male and female
- Patients who did not receive any anti-tumor therapies prior to the surgery (including liver transplantation, TACE, local tumor ablation, chemotherapy, radiotherapy, molecular targeted therapy and other anti-tumor therapy) resection of hepatocellular carcinoma
- Patients who underwent radical resection of HCC, and 1 month after surgery,dynamic computed tomography showed on lesion in the liver and no signs of extrahepatic metastasis
- Sign the informed consent
Exclusion Criteria:
- Women who were pregnant or breast-feeding
- signs showing recurrence or metastasis one month after surgery
- Recurrent HCC
- Patients unable to take drug orally
- Patients inappropriate to participate in the trial upon the investigator's judgment
Sites / Locations
- First affiliated Hospital of Xiamen UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Thalidomide
Control
Arm Description
Thalidomide 100mg per day after the radical resection HCC
No adjuvant Thalidomide treatment after curative hepatic resection
Outcomes
Primary Outcome Measures
disease-free survival
Secondary Outcome Measures
Overall survival
Full Information
NCT ID
NCT01924624
First Posted
July 21, 2013
Last Updated
August 15, 2013
Sponsor
The First Affiliated Hospital of Xiamen University
1. Study Identification
Unique Protocol Identification Number
NCT01924624
Brief Title
Adjuvant Therapy With Thalidomide After Curative Resection of Hepatocellular Carcinoma
Official Title
Adjuvant Therapy With Thalidomide After Curative Resection of Hepatocellular Carcinoma.: a Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
July 2013
Overall Recruitment Status
Unknown status
Study Start Date
July 2013 (undefined)
Primary Completion Date
August 2015 (Anticipated)
Study Completion Date
December 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The First Affiliated Hospital of Xiamen University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Postoperative recurrence of hepatocellular carcinoma (HCC) is a major problem after surgical resection. To date, adjuvant chemotherapy or other adjuvant modalities have not been proven effective in preventing or delaying recurrence. The aim of this prospective randomized study was to evaluate the effectiveness of Thalidomide as a postoperative adjuvant regimen in inhibiting the recurrence of HCC
Detailed Description
A number of modalities for preventing HCC recurrence after resection have been proposed and analyzed. Both preoperative and adjuvant transcatheter arterial chemoembolization (TACE) were found to be unable to reduce the risk of postoperative recurrence significantly, or confer a survival advantage. Vitamin K (VK) is a fat-soluble vitamin that regulates clotting factor production by acting as a coenzyme for a VK dependent carboxylase that catalyzes carboxylation of glutamic acid residues into gamma-carboxyglutamic acid. The findings in vitro have indicated that VK2 has an antiproliferative effects against hepatoma cell lines, but its efficacy in suppressing HCC recurrence was not confirmed in human studies. Interferon has a variety of biologic properties, including antiviral, immunomodulatory, antiproliferative, antiangiogenic and tumoricidal effects. It is reported that interferon is effective in preventing the development of HCC recurrence after its curative treatment in HCV-related cirrhosis. However, interferon treatment also has side-effects, including flu-like symptoms, fatigue, neutropenia, thrombocytopenia, depression, bone marrow suppression, and unmasking or exacerbation of autoimmune illnesses, which lead either to treatment disruption or dose modification. Polyprenoic acid, an acyclic retinoid, reportedly is effective in prevention of second primary hepatomas, but long-term safety and efficacy data are lacking.
Thalidomide possesses immunomodulatory,anti-inflammatory, and antiangiogenic properties.It has successfully been applied for the treatment of various malignancies including HCC.To investigated whether postoperative adjuvant therapy with Thalidomide could inhibite the recurrence of HCC after radical resection,we planed to conduct this clinical trial.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma, Recurrence
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
140 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Thalidomide
Arm Type
Experimental
Arm Description
Thalidomide 100mg per day after the radical resection HCC
Arm Title
Control
Arm Type
Active Comparator
Arm Description
No adjuvant Thalidomide treatment after curative hepatic resection
Intervention Type
Drug
Intervention Name(s)
Thalidomide
Other Intervention Name(s)
Contergan
Intervention Description
Patients in the Adjuvant group were given oral Thalidomide(at a dose of 100 mg per day) continuously during the follow-up period
Primary Outcome Measure Information:
Title
disease-free survival
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Overall survival
Time Frame
5 years
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:
18-75 years old,male and female
Patients who did not receive any anti-tumor therapies prior to the surgery (including liver transplantation, TACE, local tumor ablation, chemotherapy, radiotherapy, molecular targeted therapy and other anti-tumor therapy) resection of hepatocellular carcinoma
Patients who underwent radical resection of HCC, and 1 month after surgery,dynamic computed tomography showed on lesion in the liver and no signs of extrahepatic metastasis
Sign the informed consent
Exclusion Criteria:
Women who were pregnant or breast-feeding
signs showing recurrence or metastasis one month after surgery
Recurrent HCC
Patients unable to take drug orally
Patients inappropriate to participate in the trial upon the investigator's judgment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yan-Ming Zhou, MD
Phone
8605932139708
Ext
8605922139908
Email
zhouymsxy@sina.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yanmng Zhou, MD
Organizational Affiliation
Xiamen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
First affiliated Hospital of Xiamen University
City
Xiamen
State/Province
Fujian
ZIP/Postal Code
361003
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yan-Ming Zhou, MD
Email
zhouymsxy@sina.cn
First Name & Middle Initial & Last Name & Degree
Bin Li
First Name & Middle Initial & Last Name & Degree
Lu-Peng Wu
First Name & Middle Initial & Last Name & Degree
Xiu-Dong Li
First Name & Middle Initial & Last Name & Degree
Xu Su
12. IPD Sharing Statement
Learn more about this trial
Adjuvant Therapy With Thalidomide After Curative Resection of Hepatocellular Carcinoma
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