Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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
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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