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RCT of Different Effects of Nucleot(s)Ide Analogues on the Prognosis of HBV-HCC Patients After Curative Resection

Primary Purpose

HCC, HBV Coinfection

Status
Active
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Tenofovir Disoproxil
Entecavir
Sponsored by
West China Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HCC focused on measuring tenofovir, HBV, HCC, nucleo(t)side analogues, Entecavir

Eligibility Criteria

18 Years - 69 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. older than 18 years and less than 69 years old;
  2. HBsAg positive HCV antibody negative and HIV antibody negative;
  3. HBV-DNA>200 IU/mL;
  4. BCLC(Barcelona Clinic Liver Cancer) staging O and A stage;
  5. Platelet100×10^9/L;
  6. Liver function Child-Pugh A,with no invasion in portal vein, hepatic vein and two large branches, no extrahepatic metastasis;
  7. Creatinine clearance rate≥ 70 mL/min;
  8. Antiviral treatment was not performed before surgery or antiviral treatment was accepted in a short term (<3 months);
  9. No treatment was performed before the operation. The results of postoperatively histopathological biopsy were HCC;
  10. The patients agree to participate in the clinical trial.

Exclusion Criteria:

  1. The image found extrahepatic lymph nodes or visceral metastasis, the existence of large vascular invasion, the existence of bile duct embolus in the first operation;
  2. The patient combined with a malignant tumor of other organs or had a history of other malignant tumors in other organs;
  3. Liver function decompensation, such as: upper gastrointestinal bleeding, refractory ascites, coagulation dysfunction and so on;
  4. contraindications to surgery;
  5. Patients with poor compliance and not adhered to the follow-ups;
  6. Patients refused to participate in the clinical trial.

Sites / Locations

  • West China Hospital, Sichuan University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

ETV group

TDF group

Arm Description

group in which patients take ETV as antiviral therapy after curative treatment

group in which patients take TDF as antiviral therapy after curative treatment

Outcomes

Primary Outcome Measures

Overall survival
the difference of overall survival between two groups
Recurrence-free survival
the difference of overall survival between two groups

Secondary Outcome Measures

cytokines
several cytokines secreted by patients after antiviral therapy such as interferon λ3
Viral reactivity
HBsAg,HBsAb,HBeAg,HBeAb,HBcAb

Full Information

First Posted
July 23, 2019
Last Updated
May 23, 2022
Sponsor
West China Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04032860
Brief Title
RCT of Different Effects of Nucleot(s)Ide Analogues on the Prognosis of HBV-HCC Patients After Curative Resection
Official Title
The Different Effects of Nucleotide and Nucleoside Analogues on the Prognosis of Hepatitis B Virus-Related Hepatocellular Carcinoma Patients After Curative Resection:a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 1, 2017 (Actual)
Primary Completion Date
July 1, 2022 (Anticipated)
Study Completion Date
July 1, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
West China Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
In Asia, hepatocellular carcinoma (HCC) commonly occurred in the underlying hepatitis B virus (HBV)-related liver disease.Curative therapies could improve the prognosis of HCC patients. However, tumor recurrence after curative therapy remains high with a 5-year recurrence rate >70%.The risk for HCC development is increased for patient with HBV infection,but there was no consensus about which kind of oral antiviral treatment was the best option in the prevention of HBV related HCC recurrence after curative treatment.Therefore, we conducted this study to investigate the different effects of nucleotides(TDF) and nucleosides(ETV) on the prognosis of HBV-related HCC after curative resection.
Detailed Description
The study was designed to compare the efficacy of ETV and TDF for patients with HBV-related HCC patients undergoing curative liver resection. Eligible patients were randomly assigned in a 1:1 ratio via computer-generated allocation to either the ETV group or TDF group. A block size and strata were used in the randomization. In 2015, the American Association for the Study of Liver (AASLD) adopted ETV and TDF as first-line antiviral treatments for chronic hepatitis B. Patients in the ETV group received ETV tablets (RunZhong, CHIATAI TIANQING, China) 0.5 mg/d orally starting from 2-4 weeks before surgery; those in the TDF group receive TDF tablets(Viread, Aspen Port Elizabeth, China) 300 mg/d orally starting from 2-4 weeks before surgery. Antiviral treatment was continued unless there was unacceptable toxicity or withdrawal of consent. Preoperatively, all patients underwent chest radiography and at least 2 dynamic imaging examinations (contrast-enhanced ultrasound, contrast-enhanced computed tomography(CT) or magnetic resonance imaging(MRI)). HBsAg and hepatitis B e antigen (HBeAg), HBV-DNA load, anti-HCV, alpha-fetoprotein (AFP), carcinoembryonic antigen(CEA), carbohydrate antigen 19-9(CA19-9), liver function and HBV genotypes were serologically examined within 1 week before surgery. Additional serum samples were collected to test single-nucleotide polymorphisms(SNPs) of the interleukin 28B(IL-28B) gene and serum levels of interferon(IFN)-λ1, IFN-λ2, IFN-λ3, IL-1β, tumor necrosis factor alpha(TNF-α), IL-6, IL-8 and IL-10. All serum and DNA samples were stored at -80°C until use. After general anesthesia, surgery was performed as the standard protocol. Intraoperative ultrasonography was performed to assess the relationship of the tumor to vascular structures and to eliminate the extrahepatic metastasis. Pringle's maneuver was applied to occlude the blood inflow of the liver with cycles of 15 minutes clamp time and 5 minutes unclamped time. Liver resection was carried out by the Cusa Excel Ultrasonic Surgical Aspirator System(CUSA). In the study, the primary outcome measures included both recurrence and overall survival rates from the date of the operation. Secondary outcome measures included patient tolerance of antiviral treatment, virologic response, liver function and additional cytokines such as IFN-λ1 IFN-λ2, IFN-λ3, IL-1β, TNF-α, IL-6, IL-8 and IL-10. All the patients received follow-up monitoring 1 month after the operation, every 3 months thereafter during the first 3 years, and then every 6 months in subsequent years. Physical examination, blood cell and differential counts, renal and liver function tests, AFP levels, HBV serology and HBV-DNA levels, serum IFN-λ level and imaging examinations were included in the follow-up examinations when necessary. Follow-up was continued until August 2020 when all surviving patients had a minimum follow-up of 24 months. Tumor recurrence was diagnosed based on the identification of a new lesion on at least 2 radiological examinations and increased AFP levels (>100 ng/mL). Patients with tumor recurrence were actively treated with salvage liver transplantation, repeat hepatic resection, radiofrequency ablation, transcatheter arterial chemoembolization(TACE), sorafenib, and/or chemotherapy, depending on the extent of the disease, the liver function, and general condition of the patient.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HCC, HBV Coinfection
Keywords
tenofovir, HBV, HCC, nucleo(t)side analogues, Entecavir

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
104 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ETV group
Arm Type
Experimental
Arm Description
group in which patients take ETV as antiviral therapy after curative treatment
Arm Title
TDF group
Arm Type
Experimental
Arm Description
group in which patients take TDF as antiviral therapy after curative treatment
Intervention Type
Drug
Intervention Name(s)
Tenofovir Disoproxil
Other Intervention Name(s)
TDF
Intervention Description
patients with HBV-HCC would take TDF as antiviral therapy before curative treatment to see the prognosis after surgery
Intervention Type
Drug
Intervention Name(s)
Entecavir
Other Intervention Name(s)
ETV
Intervention Description
patients with HBV-HCC would take ETV as antiviral therapy before curative treatment to see the prognosis after surgery
Primary Outcome Measure Information:
Title
Overall survival
Description
the difference of overall survival between two groups
Time Frame
1,3,5 years
Title
Recurrence-free survival
Description
the difference of overall survival between two groups
Time Frame
1,3,5 years
Secondary Outcome Measure Information:
Title
cytokines
Description
several cytokines secreted by patients after antiviral therapy such as interferon λ3
Time Frame
1-3 years
Title
Viral reactivity
Description
HBsAg,HBsAb,HBeAg,HBeAb,HBcAb
Time Frame
1,3 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: older than 18 years and less than 69 years old; HBsAg positive HCV antibody negative and HIV antibody negative; HBV-DNA>200 IU/mL; BCLC(Barcelona Clinic Liver Cancer) staging O and A stage; Platelet100×10^9/L; Liver function Child-Pugh A,with no invasion in portal vein, hepatic vein and two large branches, no extrahepatic metastasis; Creatinine clearance rate≥ 70 mL/min; Antiviral treatment was not performed before surgery or antiviral treatment was accepted in a short term (<3 months); No treatment was performed before the operation. The results of postoperatively histopathological biopsy were HCC; The patients agree to participate in the clinical trial. Exclusion Criteria: The image found extrahepatic lymph nodes or visceral metastasis, the existence of large vascular invasion, the existence of bile duct embolus in the first operation; The patient combined with a malignant tumor of other organs or had a history of other malignant tumors in other organs; Liver function decompensation, such as: upper gastrointestinal bleeding, refractory ascites, coagulation dysfunction and so on; contraindications to surgery; Patients with poor compliance and not adhered to the follow-ups; Patients refused to participate in the clinical trial.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
He Linye, Doctor
Organizational Affiliation
Westchina Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
West China Hospital, Sichuan University
City
Chengdu
State/Province
Sichuan
ZIP/Postal Code
610000
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
de-identified individual participant data for all primary and secondary outcome measures will be made available
IPD Sharing Time Frame
Data will be available within 6 months of study completion
IPD Sharing Access Criteria
requestors will be required to sign a data access agreement
IPD Sharing URL
http://bethesda.org

Learn more about this trial

RCT of Different Effects of Nucleot(s)Ide Analogues on the Prognosis of HBV-HCC Patients After Curative Resection

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