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Precision Recurrence Risk Assessment in Early-stage Hepatocellular Carcinoma

Multimodal Deep Learning Models for Predicting Recurrence Pattern in Hepatocellular Carcinoma: A Multicenter Retrospective Development and Validation Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07030842
Enrollment
579
Registered
2025-06-22
Start date
2023-08-25
Completion date
2024-07-30
Last updated
2025-06-29

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

Conditions

Hepatocellular Carcinoma (HCC)

Keywords

artificial intelligence, recurrence pattern, multimodal, deep learning

Brief summary

This retrospective observational study aims to evaluate whether artificial intelligence (AI) models can predict aggressive recurrence in patients who underwent liver resection for early-stage hepatocellular carcinoma (HCC). The main question it seeks to answer is: Can deep learning models combining preoperative MRI, postoperative pathology slides, and clinical data accurately identify HCC patients at high risk of aggressive recurrence after surgery? To answer this, the investigators will analyze existing medical data (preoperative MRIs, postoperative whole-slide images, and clinical records) from 579 patients across two medical centers. All data will be anonymized before analysis, and no additional interventions are required from participants. This study may help clinicians stratify high-risk patients who could benefit from closer surveillance or adjuvant therapies

Interventions

PROCEDUREliver resection

This is a retrospective observational study analyzing existing clinical data; no experimental interventions were administered. The study evaluates the predictive performance of two deep learning models (preoperative and postoperative) using standard-of-care medical data collected during routine clinical practice, including: Preoperative contrast-enhanced MRI scans Postoperative hematoxylin and eosin (H&E)-stained whole slide images Clinical variables (laboratory results, pathology reports, and demographic data) All data were collected as part of standard diagnostic and treatment protocols for hepatocellular carcinoma (HCC) patients undergoing liver resection. No additional interventions or modifications to clinical care were implemented for study purposes. The artificial intelligence models were applied to previously acquired, de-identified data to predict aggressive recurrence patterns

Sponsors

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
CollaboratorOTHER
Tongji Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients who underwent curative liver resection (R0) for pathologically confirmed primary HCC * BCLC stage 0-A at diagnosis * Availability of preoperative contrast-enhanced MRI performed within 1 month before surgery * Availability of postoperative H&E-stained whole slide images (WSIs) with adequate tumor representation * Complete clinical follow-up data (minimum 2 years if no recurrence)

Exclusion criteria

* R1/R2 resection (micro/macroscopically positive margins) * Missing or poor-quality preoperative MRI (motion artifacts/insufficient contrast enhancement) * Received neoadjuvant or adjuvant therapy (to avoid treatment confounding) * Incomplete follow-up (loss to follow-up or missing recurrence status) * Non-curative procedures (e.g., palliative resection)

Design outcomes

Primary

MeasureTime frameDescription
Aggressive Recurrence Pattern2 years after surgeryDefined as first recurrence exceeding Milan criteria within 2 years after liver resection.

Secondary

MeasureTime frameDescription
Recurrence-Free Survival (RFS)From surgery until first recurrence or July 30, 2024Time from surgery date to radiologically confirmed recurrence or last follow-up (until July 30, 2024).
Overall Survival (OS)From surgery until death or July 30, 2024Time from surgery date to death from any cause or last follow-up.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026