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Clinical Trials/NCT05677724
NCT05677724
Recruiting
Not Applicable

Single-cell RNA Sequencing Resolves the Regulatory Role of HBV on the Hepatocellular Carcinoma Immune Microenvironment

Fubing Wang1 site in 1 country20 target enrollmentJuly 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
HBV
Sponsor
Fubing Wang
Enrollment
20
Locations
1
Primary Endpoint
single cell RNA sequencing
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

In summary, with the help of single-cell sequencing technology, this study aims to focus on elucidating the influence of HBV-induced hepatocellular carcinoma cell metabolic changes on microenvironment remodeling. With the help of hepatocellular carcinoma microenvironment changes, this study provide a more accurate diagnosis and treatment method for HBV-induced hepatocellular carcinoma.

Registry
clinicaltrials.gov
Start Date
July 1, 2022
End Date
June 30, 2023
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Fubing Wang
Responsible Party
Sponsor Investigator
Principal Investigator

Fubing Wang

Dr.Prof.

Zhongnan Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients with primary liver cancer (hepatocellular carcinoma (HCC)), with evidence of histological or cytological diagnosis, or with HCC meeting conventional clinical diagnostic criteria.
  • Both sexes, aged 18-80 years old
  • The results of HBVDNA test were in line with the inclusion criteria
  • The patient had at least one measurable lesion according to the Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST V1.1)
  • Agreed to comply with the study protocol for treatment and follow-up, agreed to provide clinicopathological and follow-up data required by the study, and agreed to use the study data for subsequent research and product development

Exclusion Criteria

  • Other malignant tumors;
  • Patients with severe organic diseases do not meet the requirements of infectious liver cancer in this study;
  • Suffering from mental illness cannot guarantee the compliance of this study;
  • Previous recipients of any cell or organ transplantation;
  • Received local regional liver therapy (including various ablations, percutaneous ethanol or acetic acid injections, high-intensity focused ultrasound, transarterial embolization, chemotherapy, or chemoembolization plus embolization) within 14 days prior to study treatment initiation.

Outcomes

Primary Outcomes

single cell RNA sequencing

Time Frame: within 4 hours after the sample was submitted for examination

10x genomics chromium 3' sequencing

Biochemical index detection

Time Frame: within 4 hours after the sample was submitted for examination

HbsAg (IU/mL) \\HbsAb (mIU/mL)\\HbeAg\\HbeAb\\HbcAb

HBV DNA copy number

Time Frame: within 24 hours after the sample was submitted for examination

HBV DNA (IU/mL)

Study Sites (1)

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