Clinical trial Recruiting at 1 site Observational Ages 18 and up

Using AI on CT and MRI scans to predict immunotherapy response and survival for liver cancer patients

Official title: Predicting Immunotherapy Response and Survival of Liver Cancer Patients Using Artificial Intelligence and Radiomics (Radiology-AI-Liver)

Run by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · NCT07059936 · Data updated 2026-11-12

This project will test whether artificial intelligence applied to CT and MRI scans can predict which adults with hepatocellular carcinoma will respond to immunotherapy and their likely survival.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment350 (estimated)
SponsorUnion Hospital, Tongji Medical College, Huazhong University of Science and Technology
Academic / other
Drugs / interventionsimmunotherapy
Locations1 site (Wuhan, Hubei)
StatusRecruiting
StartedJuly 2025
Main results expectedSeptember 2026
Study endsSeptember 2026
Registry record updatedJuly 22, 2025
Trial IDNCT07059936 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults over 18 with biopsy-confirmed hepatocellular carcinoma treated at Union Hospital between July 2025 and July 2026 who have at least one pre-treatment CT or MR scan are the intended participants.

Probably not a fit

Patients with poor-quality images, missing clinical data or follow-up, another primary malignancy, or an unclear pathological diagnosis are unlikely to benefit from the model.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Researchers will collect pre-treatment (and possibly post-treatment) CT and MR images from hepatocellular carcinoma patients treated at Union Hospital between July 2025 and July 2026 and link them with clinical outcomes. An automated pipeline will segment tumors, extract radiomics features, select the most informative features, and train machine-learning classification models to predict immunotherapy response and survival. Patients with poor image quality, incomplete data, another primary cancer, or unclear pathology will be excluded to preserve model reliability. The work is observational and based on retrospective clinical imaging and pathology data from a single center in Wuhan.

Why it matters

Potential benefit: If successful, the approach could help personalize treatment by identifying patients likely to benefit from immunotherapy and avoiding ineffective therapies for others.

How similar studies have gone: Previous small studies using radiomics and AI to predict immunotherapy response in liver cancer have shown promise but remain exploratory and not yet widely validated.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Patients were treated for hepatocellular carcinoma in Wuhan Union Hospital from July 2025 to July 2026;
2. Aged \> 18 years old;
3. At least one CT scan or MR scan before treatment;
4. Tissue biopsy pathological examination confirmed the diagnosis of the above tumors.

Exclusion criteria:

1. Poor image quality;
2. Incomplete clinical data or loss of follow-up;
3. Presence of another primary malignancy other than liver cancer;
4. Unclear pathological diagnosis.

Where it's running

  • Union Hospital,Tongji Medical College,Huazhong University of Science and Technology
    Wuhan, Hubei, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.