Actively Recruiting

Age: 18Years - 70Years
All Genders
ID07101237

An Exploratory Study Combining Multimodal Imaging and Multi-omics Analysis to Improve Precision Diagnosis and Treatment in Primary Liver Cancer

Led by Peking Union Medical College Hospital · Updated on 2025-08-03

308

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Primary liver cancer, including hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinoma (ICC), is a major cause of cancer-related deaths. This research aims to improve how liver cancer is diagnosed and treated by combining advanced imaging techniques with molecular and genetic analysis. The study focuses on understanding tumor differences at multiple levels to guide precise clinical decisions and better predict patient outcomes. The study uses a multi-modal ultrasonic imaging system that includes conventional ultrasound, superb microvascular imaging (SMI), shear wave and strain elastography, and contrast-enhanced ultrasound (CEUS). These imaging tests will be conducted at multiple time points before and after surgery or conversion therapy, up to five years. Additionally, tumor tissue and blood samples will be collected to study protein and gene characteristics using photoacoustic imaging (PAI) and multi-omics analysis. Artificial intelligence (AI) will be applied to integrate imaging and molecular data to develop models predicting tumor behavior and prognosis. Participants will undergo detailed ultrasound examinations performed by experienced sonographers in specific body positions. Blood and tumor samples will be collected for laboratory analyses. Follow-up visits will occur regularly over several years to monitor tumor progression or treatment outcomes. The main outcome measured is the time until tumor progression or failure to follow up, assessed for up to five years. This comprehensive approach aims to provide new tools for precise diagnosis and personalized treatment planning in liver cancer care.

CONDITIONS

Brief Title

An Exploratory Study on Developing an Integrated Approach Combining Multimodal Imaging and Multi-omics Characterization of Tumor Heterogeneity for Precision Diagnosis and Treatment Optimization in Liver Cancer.

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 18 and up to 70 years
  • Both males and females are eligible
  • Diagnosed with primary hepatocellular carcinoma (HCC) or intrahepatic cholangiocarcinoma (ICC)
  • Scheduled for surgical resection or conversion therapy
  • Pathological confirmation of HCC or ICC via surgery or biopsy
  • Tumor lesion located 8 cm or less from the skin surface
Not Eligible

You will not qualify if you...

  • Pregnancy, breastfeeding, or planning pregnancy during the study
  • History of other cancers
  • Heart, lung, brain, or kidney failure
  • Tumor lesion deeper than 8 cm from the skin surface on ultrasound
  • Presence of large amounts of ascites
  • Inability to follow study procedures, such as holding breath during imaging
  • Allergy to ultrasound contrast agents

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 5 years

Participants undergo conventional ultrasound, superb microvascular imaging (SMI), shear wave/strain elastography, and contrast enhanced ultrasound (CEUS) to collect multimodal imaging data for liver cancer assessment.

Baseline imaging and follow-up imaging visits at 1, 2, 3, 4, 5, 6, 9, 12, 15, 18, 21, 24, 30, 36, 42, 48, 54, and 60 months after surgery or conversion therapy

Sample Collection

Duration - Concurrent with diagnostic evaluation

Peripheral venous blood samples and tumor specimens are collected to analyze transcriptomic and proteomic profiles and study tumor heterogeneity.

Blood and tumor sample collection visits aligned with diagnostic imaging schedule

Long-term Monitoring

Duration - Up to 5 years

Participants are monitored up to 5 years for tumor progression or follow-up failure to assess prognosis using integrated imaging and multi-omics data.

Ongoing follow-up visits as per imaging schedule

Trial Site Locations

Total: 1 location

1

Peking Union Medical College Hospital

Beijing, China, 100730

Actively Recruiting

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Research Team

M

Meng Yang, Doctor

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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