Radiofrequency Ablation Combined With Recombinant Human Adenovirus Type 5 in the Treatment of Hepatocellular Carcinoma.

Sponsor
Southwest Hospital, China (Other)
Overall Status
Unknown status
CT.gov ID
NCT03790059
Collaborator
(none)
160
2
2
47
80
1.7

Study Details

Study Description

Brief Summary

The primary reason for recurrence of hepatocellular carcinoma after radiofrequency ablation (RFA) is the micro-metastatic lesion that has not been ablated and inactivated in the transitional area.Some clinical trials have confirmed that H101(recombinant human adenovirus type 5 injection) has selective oncolysis in a variety of solid tumors.However, there are no reports that H101 which is injected during surgery can improve the efficacy of RFA in liver cancer at present.Therefore,We used a multicenter prospective randomized controlled study as the main method to prospectively compare the short-term and long-term efficacy of RFA combined with H101 group and traditional RFA group in the treatment of small liver cancer (single lesion , diameter less than or equal to 3cm,to evaluate the value of RFA combined with H101 injection in reducing the postoperative recurrence rate of small hepatocellular carcinoma, and to provide a reliable evidence-based medical basis for the selection of treatment methods for small hepatocellular carcinoma.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

The primary reason for recurrence of hepatocellular carcinoma after radiofrequency ablation (RFA) is the micro-metastatic lesion that has not been ablated and inactivated in the transitional area.Oncolytic virus H101 is a genetically engineered adenovirus that lacks Elb 55ku protein.Some clinical trials have confirmed that H101 has selective oncolysis in a variety of solid tumors.Furthermore,research shows that the directly dissolving tumor activity of H101 enhanced obviously and activate the body's anti-tumor immune to induce the distal antitumor effect under the condition of mild high temperature (40 ℃ and 42 ℃).The transition zone of RFA can provide the appropriate mild high temperature.However, there are no reports that H101 which is injected during surgery can improve the efficacy of RFA in liver cancer at present.Therefore,We used a multicenter prospective randomized controlled study as the main method to prospectively compare the short-term and long-term efficacy of RFA combined with H101 group and traditional RFA group in the treatment of small liver cancer (single lesion , diameter less than or equal to 3cm,to evaluate the value of RFA combined with H101 injection in reducing the postoperative recurrence rate of small hepatocellular carcinoma, and to provide a reliable evidence-based medical basis for the selection of treatment methods for small hepatocellular carcinoma.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
160 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Radiofrequency Ablation Combined With Local Injection of Recombinant Human Adenovirus Type 5 in the Treatment of Hepatocellular Carcinoma:A Multicenter Prospective Randomized Controlled Trial.
Study Start Date :
Oct 1, 2016
Anticipated Primary Completion Date :
Sep 1, 2020
Anticipated Study Completion Date :
Sep 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: RFA combined with H101 group

The experimental group was RFA combined H101.H101 has oncolysis in HCC after RFA and reduce tumor recurrence.

Drug: H101
Intraoperative injection of H101 can improve the efficacy of RFA in hepatocellular carcinoma.
Other Names:
  • Recombinant Human Adenovirus Type 5 Injection(H101).
  • Procedure: RFA
    Treat the samll HCC with the RFA.
    Other Names:
  • Radiofrequency ablation(RFA).
  • Other: Conventional RFA group

    The standard control group was the conventional RFA.Using RFA for the treatment of small HCC.The efficacy was compared with that of the experimental group combined with H101.

    Procedure: RFA
    Treat the samll HCC with the RFA.
    Other Names:
  • Radiofrequency ablation(RFA).
  • Outcome Measures

    Primary Outcome Measures

    1. Tumor-free survival [two-years tumor-free survival.]

      Postoperative tumor-free survival is an evaluation of tumor recurrence and metastasis.It's also an evaluation of the efficacy of the experimental group

    Secondary Outcome Measures

    1. Overall survival [two-years overall survival.]

      The percentage of patients who receive certain treatments and are still alive after years of follow-up.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. The patients understand the content and significance of the study and we obtain a written informed consent from them.

    2. The patients' gender are not limited and are between the ages of 18 and 75.

    3. Liver function of Child-Pugh Class A or B;The retention rate of indocyanine green for 15 minutes is less than or equal to 20%.

    4. The ECOG score is 0.

    5. The diagnosis was a single hepatocellular carcinoma with a diameter of no more than 3cm.

    6. There were no other related diseases affecting RFA treatment.

    Exclusion Criteria:
    1. There are tumor emboli in the large vessels of the liver;distant metastasis of HCC.

    2. The patient has or has had a history of refractory ascites,hepatic encephalopathy, or esophageal varices hemorrhage.

    3. The patient was complicated with other malignant tumors.

    4. The patient has severe cardiac, renal and other organ dysfunction.

    5. In addition to viral hepatitis, there are other active infectious diseases.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Institute of hepatobiliary surgery,Southwest Hospital Chongqing Chongqing China 400038
    2 Institute of hepatobiliary surgery,Southwest Hospital Chongqing China 400038

    Sponsors and Collaborators

    • Southwest Hospital, China

    Investigators

    • Study Director: Kuansheng Ma, Ph.D, Institute of hepatobiliary surgery,Southwest Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    fengkai, Principal Investigator, Southwest Hospital, China
    ClinicalTrials.gov Identifier:
    NCT03790059
    Other Study ID Numbers:
    • SWH2016LCYB-11
    First Posted:
    Dec 31, 2018
    Last Update Posted:
    Oct 16, 2019
    Last Verified:
    May 1, 2019
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by fengkai, Principal Investigator, Southwest Hospital, China
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 16, 2019