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Sorafenib Combined With Aspirin to Prevent the Recurrence in High-risk Patients With Hepatocellular Carcinoma

Primary Purpose

Hepatocellular Carcinoma

Status
Terminated
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
control
sorafenib
aspirin
Sponsored by
Fudan University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatocellular Carcinoma

Eligibility Criteria

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

Inclusion Criteria:

  • The characteristics of the treatment history:

    1. No sorafenib treatment history, no sorafenib allergies.
    2. No chemotherapy, radiotherapy and transcatheter arterial chemoembolization(TACE) treatment history before surgery.
  • The characteristics of the tumor:

    1. The pathological results is hepatocellular carcinoma.
    2. Meet any of the following articles:

      • Pathological prompt microvascular invasion(MVI) class II, and incorporate any of the following:Tumor number>3,Tumor size>8cm,Tumor margin is not clear and no complete capsule.
      • With the embolus in Portal vein, hepatic vein or bile duct.
      • Preoperative rupture or invasion the adjacent organs.
      • The positive cut edge.
      • Residual lesions showed by Postoperative digital subtraction angiography(DSA).
      • Alpha fetoprotein(AFP) did not drop to normal range two months after surgery.
  • The characteristics of the patients:

    1. The patient age was between 18-75.
    2. The American Society of Anesthesiologists(ASA)score was I-III.
    3. No history of esophageal varices and gastrointestinal bleeding.
    4. The Child-pugh score was A.
    5. Routine blood test: the leukocyte>2.5*10^9, platelet> 60*10^9.
    6. The Prothrombin time was prolonged less than 2 second.
    7. The Eastern Cooperative Oncology Group(ECOG) score was less than 2 points

Exclusion Criteria:

  • Sorafenib treatment before surgery.
  • Pregnant or lactating women.
  • The Child-pugh score was B-C.
  • Patients with other malignant tumor.
  • Patients with mental illness.
  • Patients participated in other clinical trials in last three months.

Sites / Locations

  • Huashan hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Placebo Comparator

Active Comparator

Active Comparator

Arm Label

control

sorafenib

sorafenib and aspirin

Arm Description

just follow up after liver resection in HCC patients

use sorafenib after liver resection in HCC patients

use sorafenib and aspirin after liver resection in HCC patients

Outcomes

Primary Outcome Measures

Overall survival

Secondary Outcome Measures

Disease free survival
Number of patients with treatment-related bleedings who use aspirin

Full Information

First Posted
April 12, 2016
Last Updated
February 11, 2019
Sponsor
Fudan University
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1. Study Identification

Unique Protocol Identification Number
NCT02748304
Brief Title
Sorafenib Combined With Aspirin to Prevent the Recurrence in High-risk Patients With Hepatocellular Carcinoma
Official Title
A Prospective Randomized Control Trial of the Effect of Sorafenib Combined With Aspirin in Preventing the Recurrence in High-risk Patients With Hepatocellular Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Terminated
Why Stopped
The enrollment of this study was slow. With the approval of lenvatinib in HCC,many patients choose the new drug, so subsequent enrollment may be more difficult.
Study Start Date
April 2016 (undefined)
Primary Completion Date
February 11, 2019 (Actual)
Study Completion Date
February 11, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fudan University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to observe the effect of sorafenib combined with aspirin in preventing the recurrence in high-risk patients with hepatocellular carcinoma.
Detailed Description
The recurrence of hepatocellular carcinoma(HCC)is the main problem during the treatment. Although some methods such as interferon may be effective in preventing the recurrence, there is still no clear effective approach widely accepted for everyone. Sorafenib, a kind of tyrosine kinase inhibitor, which inhibiting proliferation and inducing apoptosis of tumor cell by inhibiting the raf/MEK/ERK pathway, and anti-angiogenesis by targeting Vascular Endothelial Growth Factor Receptor(VEGFR), has now become the standard treatment of advanced HCC patients. Although the STORM studies have shown that adjuvant sorafenib for such patients did not significantly affect recurrence-free survival, time to recurrence, or overall survival. The patients recruiting in the study were mostly early stage, for middle and late stage patients, whether sorafenib can reduce tumor recurrence after surgical resection and prolong survival remains to be further study. Aspirin is a kind of nonsteroidal anti-inflammatory drugs. It is the first hint of aspirin's potential role in tumor prevention and treatment when Gasic found that tumor metastasis is reduced in thrombocytopenia mice, and then the research confirmed that aspirin treatment can significantly reduce the tumor metastasis. In recent years, a lot of epidemiological evidence and clinical trials found that aspirin played an important role in cancer prevention, at the same time, more experimental study has found that it can also play a role in tumor treatment. Our previous animal experiments found that a combination of sorafenib and aspirin can reverse the negative effect of sorafenib which promoted tumor metastasis, and obviously prolong survival of a tumor-burdened nude mice. So, the study is to observe the effect of sorafenib combined with aspirin in preventing the recurrence in high-risk patients with hepatocellular carcinoma.

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
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
52 (Actual)

8. Arms, Groups, and Interventions

Arm Title
control
Arm Type
Placebo Comparator
Arm Description
just follow up after liver resection in HCC patients
Arm Title
sorafenib
Arm Type
Active Comparator
Arm Description
use sorafenib after liver resection in HCC patients
Arm Title
sorafenib and aspirin
Arm Type
Active Comparator
Arm Description
use sorafenib and aspirin after liver resection in HCC patients
Intervention Type
Other
Intervention Name(s)
control
Intervention Description
just follow up
Intervention Type
Drug
Intervention Name(s)
sorafenib
Other Intervention Name(s)
sorafenib treatment
Intervention Description
sorafenib 400mg bid po
Intervention Type
Drug
Intervention Name(s)
aspirin
Other Intervention Name(s)
aspirin treatment
Intervention Description
aspirin 100mg qd po
Primary Outcome Measure Information:
Title
Overall survival
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Disease free survival
Time Frame
5 years
Title
Number of patients with treatment-related bleedings who use aspirin
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: The characteristics of the treatment history: No sorafenib treatment history, no sorafenib allergies. No chemotherapy, radiotherapy and transcatheter arterial chemoembolization(TACE) treatment history before surgery. The characteristics of the tumor: The pathological results is hepatocellular carcinoma. Meet any of the following articles: Pathological prompt microvascular invasion(MVI) class II, and incorporate any of the following:Tumor number>3,Tumor size>8cm,Tumor margin is not clear and no complete capsule. With the embolus in Portal vein, hepatic vein or bile duct. Preoperative rupture or invasion the adjacent organs. The positive cut edge. Residual lesions showed by Postoperative digital subtraction angiography(DSA). Alpha fetoprotein(AFP) did not drop to normal range two months after surgery. The characteristics of the patients: The patient age was between 18-75. The American Society of Anesthesiologists(ASA)score was I-III. No history of esophageal varices and gastrointestinal bleeding. The Child-pugh score was A. Routine blood test: the leukocyte>2.5*10^9, platelet> 60*10^9. The Prothrombin time was prolonged less than 2 second. The Eastern Cooperative Oncology Group(ECOG) score was less than 2 points Exclusion Criteria: Sorafenib treatment before surgery. Pregnant or lactating women. The Child-pugh score was B-C. Patients with other malignant tumor. Patients with mental illness. Patients participated in other clinical trials in last three months.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lunxiu Qin, MD
Organizational Affiliation
Department of general surgery, Huashan hospital, Fudan University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Huashan hospital
City
Shanghai
ZIP/Postal Code
200040
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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Sorafenib Combined With Aspirin to Prevent the Recurrence in High-risk Patients With Hepatocellular Carcinoma

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