Radiomics for Diagnosing Liver Diseases and Evaluating Progression

September 1, 2021 updated by: Rongqin Zheng, Third Affiliated Hospital, Sun Yat-Sen University

the Department of Medical Ultrasonics, Third Affiliated Hospital of Sun Yat-Sen University, 600 Tianhe Road, Guangzhou, China.

Liver diseases are worldwide problems. liver fibrosis and hepatocellular carcinoma are mostly concerned by clinicians. Radiomcis can improve diagnosis accuracy and evaluate disease progression. Hence,investors try to combine radiomics and ultrasound images together in order to improve diagnosis performances of liver fibrosis, benign and malignant tumor and progression after liver ablations.

Study Overview

Status

Enrolling by invitation

Intervention / Treatment

Detailed Description

Liver diseases are worldwide problems including diffuse hepatitis disease and liver space occupying lesions. Hepatitis B virus infection is the most important one among difuse hepatitis disease. There are 240 million people infected with HBV globally, and more than one-third of these patients (approximately 93 million) live in China. For them, a precise estimation of the degree of liver fibrosis is important for estimation of prognosis, surveillance, and treatment decisions in patients with HBV infection. Hepatocellular carcinoma is usually detected in liver space occupying lesions and leading to third common death of cancer. Hence, precise diagnosis between benign and malignant tumor is of great significance. Many guidelines recommend ablation as first line treatment to small hepatocellular carcinoma, especially to those less than 1mm.

Liver biopsy has been considered the gold standard for assessing liver diseases. However, it is limited because of sample errors, interobserver variability and many complications, such as pain, bleeding and even death. CT/MR are alternative ways with high cost and complications. Ultrasound was a first optional tool to diagnose liver disease. However, there are still some problems remained to solve:first, the diagnosis accuracy of liver fibrosis remained to be improved. Second,the diagnosis performances for distinguishing benign and malignant tumor were poor. Third, there were not objective way to assess progression after liver ablations.

Radiomcis refers to the extraction and analysis of large amounts of image features from medical images. Previous studies showed that it can improve diagnosis accuracy and evaluating disease progression. Hence,we tried to combined radiomics and ultrasound images together in order to improve diagnosis performances of liver fibrosis, benign and malignant tumor and progression after liver ablations.

Study Type

Observational

Enrollment (Anticipated)

3000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Guangdong
      • Guangzhou, Guangdong, China
        • The department of Ultrasound, the third affiliated hospital of Sun Yat-son University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

chronic hepatitis B patients /patients with liver space occupying lesions / patients after ablation

Description

For chronic hepatitis patients to assess liver biopsy

Inclusion Criteria:

  • HBsAg positive or HBV-DNA detected
  • agreed to undergo liver biopsy
  • agreed to participated in our study

Exclusion Criteria:

  • combined with other liver disease(eg. HAV/HCV/HDV,alcoholic liver disease)
  • combined with HIV
  • combined with malignant liver space occupying lesions
  • liver transplantation
  • pregnant
  • the sample size of liver biopsy could not demand: length lower than 15mm, portal areas less than 6.

For patients classified between benign and malignant tumor

Inclusion Criteria:

  • patients diagnosed with liver space occupying lesions
  • with histology results of liver space occupying lesions.
  • agreed to participate in our study and signed informed consent.

Exclusion Criteria:

  • ultrasound images cant meet the demand for analysis
  • without histology results

For patients to estimate progression after ablation

Inclusion Criteria:

  • patients diagnosed with hepatocellular carcinoma;
  • patients treated with ablation;
  • patients performed the contrast-enhanced ultrasonography before ablation;
  • patients who treated with transcatheter arterial chemoembolization (TACE) performed the contrast-enhanced ultrasonography performed before TACE;

Exclusion Criteria:

  • patients with lack of US digital imaging data
  • loss to follow-up

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
chronic hepatitis B patients
ultrasound and radiomics
patients with liver space occupying lesions
ultrasound and radiomics
patients undergo ablation
ablation, ultrasound and radiomics

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
liver fibrosis
Time Frame: 1 year
the degree of liver fibrosis
1 year
benign or malignance
Time Frame: 5 years
the malignance of liver space occupying lesions
5 years
The incidence of recurrence
Time Frame: 5 years
the incidence of liver cancer recurrence after ablation
5 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: rongqin zheng, doctor, The department of Ultrasound, the third affiliated hospital of Sun Yat-sen University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2011

Primary Completion (Anticipated)

December 31, 2022

Study Completion (Anticipated)

December 31, 2022

Study Registration Dates

First Submitted

July 14, 2017

First Submitted That Met QC Criteria

July 14, 2017

First Posted (Actual)

July 18, 2017

Study Record Updates

Last Update Posted (Actual)

September 2, 2021

Last Update Submitted That Met QC Criteria

September 1, 2021

Last Verified

September 1, 2021

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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