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AI Multimodal Model for Liver Cancer Diagnosis and Prognosis

A Comprehensive Study of Liver Cancer Diagnosis and Prognosis Prediction Based on Artificial Intelligence and Multimodal Data

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07658586
Acronym
AIM-LCAP
Enrollment
600
Registered
2026-06-22
Start date
2025-12-01
Completion date
2028-12-01
Last updated
2026-07-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatocellular Carcinoma, Intrahepatic Cholangiocarcinoma (Icc), Liver Cancer

Brief summary

This study aims to develop a comprehensive artificial intelligence model system integrating preoperative multimodal data (CT/MRI imaging, clinical laboratory data, and radiology report text) to achieve two core objectives. First, to develop a multimodal fusion diagnostic model for non-invasive and accurate preoperative differentiation of liver cancer subtypes, including distinguishing benign from malignant lesions and differentiating hepatocellular carcinoma from intrahepatic cholangiocarcinoma. Second, to develop a prognostic prediction model for patients with confirmed liver cancer undergoing radical surgery to assess postoperative progression-free survival and overall survival. This is a multicenter retrospective cohort study with an anticipated sample size of ≥600 patients. Model performance will be evaluated using AUC, accuracy, sensitivity, specificity, C-index, and calibration curves. Subgroup analysis will be conducted based on whether patients received neoadjuvant therapy.

Interventions

None listed

Sponsors

Guangxi Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

-Diagnostic Model Cohort: * Age ≥18 years * Underwent preoperative contrast-enhanced CT or MRI for clinically suspected liver space-occupying lesion * Have complete preoperative clinical laboratory data * Have complete original CT/MRI imaging data and radiology reports * Have definite pathological diagnosis from surgery or biopsy as gold standard Prognostic Prediction Model Cohort (selected from diagnostic cohort): * Meet all diagnostic cohort inclusion criteria * Pathologically confirmed liver cancer * Underwent radical hepatectomy * Have complete preoperative multimodal data (CT/MRI imaging, clinical laboratory data, radiology reports) * Have complete postoperative follow-up data to determine progression-free survival and overall survival endpoints and time (minimum follow-up of 24 months)

Exclusion criteria

* · Key clinical, imaging, or pathological data severely missing or incomplete * Preoperative CT or MRI images of poor quality or missing sequences, unable to perform reliable image analysis * Prior local treatment for the target liver lesion, unless clearly recorded as neoadjuvant therapy before surgery * Concurrent other malignant tumors * Lost to follow-up or follow-up data cannot meet endpoint determination requirements

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic Accuracy of the Multimodal AI Model for Liver Lesion ClassificationAt the time of initial diagnosisThe diagnostic performance of the multimodal AI model in differentiating benign from malignant liver lesions and distinguishing hepatocellular carcinoma from intrahepatic cholangiocarcinoma, evaluated using pathology results as the gold standard. Performance metrics include area under the receiver operating characteristic curve (AUC), accuracy, sensitivity, and specificity.
Prognostic Performance of the Multimodal AI Model for Postoperative Survival Predictionminimum follow-up of 24 monthsThe prognostic performance of the multimodal AI model in predicting postoperative progression-free survival (PFS) and overall survival (OS) in patients with pathologically confirmed liver cancer who underwent radical hepatectomy. Performance metric includes the concordance index (C-index). Calibration curves are also assessed.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 2, 2026