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Integrating Multimodal AI to Predict Treatment Response and Refine Risk Stratification in Esophageal Cancer (Radiogenomics-Esophagus)

Multimodal AI-based Therapy Response Prediction and Risk Stratification for Esophageal Cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07354295
Enrollment
1500
Registered
2026-01-21
Start date
2025-07-26
Completion date
2030-09-30
Last updated
2026-03-10

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

Conditions

Esophageal Cancer

Keywords

Esophageal Cancer; AI; prediction; prognosis

Brief summary

This AI-driven model leverages multimodal data-such as radiomics, pathomics, genomics, and broader multi-omics profiles-to capture complementary aspects of tumor biology and predict treatment response and prognosis.

Detailed description

Built upon retrospective cohorts for model development and rigorously validated in prospective cohorts, the proposed AI predictive model integrates multimodal data (radiomics, pathomics, genomics, and multi-omics)-each reflecting distinct dimensions of tumor heterogeneity-to enable joint prediction of treatment response and clinical outcomes.

Interventions

None listed

Sponsors

Shu Peng
Lead SponsorOTHER
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
CollaboratorOTHER
The First Affiliated Hospital of Henan University of Science and Technology
CollaboratorOTHER
Henan Provincial People's Hospital
CollaboratorOTHER
Zhongnan Hospital
CollaboratorOTHER
Renmin Hospital of Wuhan University
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. Histopathologically diagnosed esophageal cancer 2. Complete baseline clinical data available (including demographic characteristics, ECOG performance score, TNM staging, etc.) 3. No other primary malignant tumors 4. Provision of informed consent 5. Availability of pre-treatment CT imaging

Exclusion criteria

1. Imaging data quality insufficient for analysis 2. Presence of another primary malignant tumor 3. Severe systemic disease

Design outcomes

Primary

MeasureTime frameDescription
overall survivalFrom enrollment to the end of treatment at 3 yearsoverall survival rate in 3-years

Countries

China

Contacts

CONTACTShu Peng, Doctor
drpeng90@hotmail.com+8618571716422

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026