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RECRUITING
NCT07849608

Silent Evaluation of DeepTRG for Assessing Tumor Response After Preoperative Treatment in Stomach and Gastroesophageal Junction Cancer

Sponsor: Qun Zhao

View on ClinicalTrials.gov

Summary

This study will evaluate whether an artificial intelligence (AI) system called DeepTRG can reliably assess cancer tissue removed during surgery after treatment given before surgery. It will include adults with stomach cancer or cancer at the junction between the stomach and the food pipe who have received treatment before surgery. Pathologists are doctors who examine tissue to diagnose disease. After cancer surgery, they assess how much living cancer remains and whether cancer is present in nearby lymph nodes. DeepTRG analyzes digital images of tissue slides to measure remaining cancer and describe tissue changes, such as scarring and inflammation. It combines information from the original tumor site and lymph nodes to produce a structured assessment. The main question is: \* How often can DeepTRG complete the required assessment and produce a clear result without a person correcting the AI analysis? The study will also examine: * How closely the system's measurements agree with assessments made by independent expert pathologists. * How accurately it detects remaining cancer, including small amounts of cancer and cancer in lymph nodes. * How long the analysis takes and how often it fails or produces an uncertain result. * Whether its performance differs across treatment types and cancer tissue types. This study will take place at the Fourth Hospital of Hebei Medical University in China. Eligible patients will be enrolled consecutively. Researchers will use tissue collected during the patients' planned surgery. No additional surgery or biopsy is required for this study. DeepTRG will run in the background in "silent mode." The doctors responsible for the patients' routine pathology reports and treatment decisions will not receive its results. Patients will continue to receive usual care. The AI model and its grading rules will be fixed before validation begins. Independent expert pathologists will assess the tissue without seeing the AI results. Researchers will then compare the expert assessments, routine pathology reports, and DeepTRG outputs. Cases with poor-quality images, failed analyses, or uncertain outputs will remain part of the assessment of how reliably the system works. Researchers will also collect information about subsequent treatment, cancer recurrence, and survival during follow-up. The initial analysis will focus on feasibility and measurement performance. A separate future study would be needed to determine whether using DeepTRG in clinical care improves doctors' decisions or patient outcomes.

Official title: Prospective Observational Study of the Feasibility and Accuracy of DeepTRG for Automated Pathological Response Assessment After Neoadjuvant Therapy in Gastric and Gastroesophageal Junction Adenocarcinoma: A Single-Center Silent Validation Study

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

200

Start Date

2026-09-01

Completion Date

2026-12-30

Last Updated

2026-09-30

Healthy Volunteers

Not specified

Interventions

DIAGNOSTIC_TEST

AI-Based Digital Pathology Assessment of Treatment Response (DeepTRG)

DeepTRG is an AI-based digital pathology system applied to whole-slide images of routinely collected hematoxylin and eosin-stained tissue from the primary tumor site and regional lymph nodes after neoadjuvant therapy and surgical resection. It quantifies residual viable tumor and treatment-related tissue changes and generates a patient-level pathological response grade with quality and uncertainty indicators. The model and grading rules will be locked before prospective validation. The system will operate in silent mode: outputs will be stored for research and withheld from treating clinicians and routine reporting pathologists. Results will be compared with routine pathology reports and independent expert assessments. Processing time, analysis failures, and uncertain outputs will be recorded. No additional biopsy or change in treatment will be required.

Locations (1)

the Fourth Hospital of Hebei Medical University

Shijiazhuang, None Selected, China