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Intraoperative Chemotherapy Against Hepatocellular Carcinoma Recurrence

Primary Purpose

Hepatocellular Carcinoma

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
sustained released 5-FU and sustained released cisplatin
sustained released 5-FU
TACE
Sponsored by
Eastern Hepatobiliary Surgery Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hepatocellular Carcinoma focused on measuring hepatocellular carcinoma, liver resection, intraoperative chemotherapy

Eligibility Criteria

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

Inclusion Criteria:

  1. tumor >5cm;
  2. multiple tumor located in one liver lobe;
  3. margin of tumor is not clear;
  4. cutting edge to tumor <1cm;
  5. portal vein branch invasion;
  6. without extra-liver metastasis;
  7. patient's liver function and condition is able to accept hepatectomy.

Exclusion Criteria:

  1. single tumor <=5cm;
  2. multiple tumor located more than in one liver lobe;
  3. margin of tumor is clear;
  4. cutting edge to tumor >=1cm;
  5. portal vein stem invasion
  6. extra-liver metastasis;
  7. patient's liver function and condition cannot accept hepatectomy.

Sites / Locations

  • Eastern Hepatobiliary Surgery Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Experimental

Arm Label

5-FU+Cisplatin

5-FU

control

Arm Description

50 HCC patients will be implanted 600mg sustained released 5-FU and 60mg sustained released cisplatin into liver incisal margin after tumor is resected.

50 HCC patients will be implanted 600mg sustained released 5-FU into liver incisal margin after tumor is resected.

Outcomes

Primary Outcome Measures

disease free survival

Secondary Outcome Measures

overall survival

Full Information

First Posted
January 4, 2009
Last Updated
March 29, 2016
Sponsor
Eastern Hepatobiliary Surgery Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00817895
Brief Title
Intraoperative Chemotherapy Against Hepatocellular Carcinoma Recurrence
Official Title
Clinical Randomized Control Trial of Intraoperative Implanting Chemotherapeutic Drugs Sustained Release Following Resection of Hepatocellular Carcinoma Against Postoperative Short-term Recurrence
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
December 2008 (undefined)
Primary Completion Date
December 2009 (Actual)
Study Completion Date
December 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Eastern Hepatobiliary Surgery Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Hepatectomy is still the most important treatment for HCC.High recurrence rate mostly influence it's prognosis, especially for the patient with tumor >5cm, multiple tumor and who cannot accept R0 resection.Our retrospective study showed sustained released 5-FU implanted into the liver incisal margin after tumor was resected could reduce the recurrence rate of HCC after liver resection.According to this, we proceed this RCT to prospectively observe the effect of sustained released 5-FU,and we also want to know whether combined with sustained released cisplatin will get better effect in preventing the tumor recurrence,especially in short time after liver resection.
Detailed Description
150 HCC patients with tumor >5cm, multiple tumor and who cannot accept R0 resection will be randomized divided into 3 groups. Group A (50 cases) will be implanted 600mg sustained released 5-FU into liver incisal margin after tumor is resected. Group B (50 cases) will be implanted 600mg sustained released 5-FU and 60mg sustained released cisplatin. Group C (50 cases) will be the controlled one which will not be implanted any chemotherapeutic drugs. All patients will accepted TACE 30 days after liver resection. We will follow up all patients until they are dead or missed connected. Related adverse reaction will be recorded. Total survival time (TST) and disease free survival time (DFST) will be calculated too. At the end of the study we will compare the difference of adverse reaction, complication, TST and DFST between the 3 groups. According to the result we will estimate these drugs' antitumor effect and safety.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma
Keywords
hepatocellular carcinoma, liver resection, intraoperative chemotherapy

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
5-FU+Cisplatin
Arm Type
Experimental
Arm Description
50 HCC patients will be implanted 600mg sustained released 5-FU and 60mg sustained released cisplatin into liver incisal margin after tumor is resected.
Arm Title
5-FU
Arm Type
Active Comparator
Arm Description
50 HCC patients will be implanted 600mg sustained released 5-FU into liver incisal margin after tumor is resected.
Arm Title
control
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
sustained released 5-FU and sustained released cisplatin
Other Intervention Name(s)
5-FU+Cisplatin group
Intervention Description
600mg sustained released 5-FU and 60mg sustained released cisplatin will be implanted into liver incisal margin after tumor is resected.
Intervention Type
Drug
Intervention Name(s)
sustained released 5-FU
Other Intervention Name(s)
5-FU group
Intervention Description
600mg sustained released 5-FU will be implanted into liver incisal margin after tumor is resected.
Intervention Type
Procedure
Intervention Name(s)
TACE
Other Intervention Name(s)
Postoperative TACE
Intervention Description
All patients will accept TACE one month after tumor was resected.
Primary Outcome Measure Information:
Title
disease free survival
Time Frame
2 years
Secondary Outcome Measure Information:
Title
overall survival
Time Frame
2 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: tumor >5cm; multiple tumor located in one liver lobe; margin of tumor is not clear; cutting edge to tumor <1cm; portal vein branch invasion; without extra-liver metastasis; patient's liver function and condition is able to accept hepatectomy. Exclusion Criteria: single tumor <=5cm; multiple tumor located more than in one liver lobe; margin of tumor is clear; cutting edge to tumor >=1cm; portal vein stem invasion extra-liver metastasis; patient's liver function and condition cannot accept hepatectomy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shen Feng, MD.
Organizational Affiliation
Eastern Hepatobiliary Surgery Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Eastern Hepatobiliary Surgery Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200438
Country
China

12. IPD Sharing Statement

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Intraoperative Chemotherapy Against Hepatocellular Carcinoma Recurrence

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