Silent Evaluation of DeepTRG for Assessing Tumor Response After Preoperative Treatment in Stomach and Gastroesophageal Junction Cancer
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
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.
Descripción general del estudio
Estado
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Ping'an Ding
- Número de teléfono: 031186095363
- Correo electrónico: ding_ping_an@hebmu.edu.cn
Ubicaciones de estudio
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None Selected
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Shijiazhuang, None Selected, Porcelana, 050011
- Reclutamiento
- the Fourth Hospital of Hebei Medical University
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Contacto:
- Ping'an Ding
- Número de teléfono: 031186095363
- Correo electrónico: ding_ping_an@hebmu.edu.cn
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Consecutive adults with histologically confirmed gastric or Siewert type II or III gastroesophageal junction adenocarcinoma who have received neoadjuvant treatment and are scheduled for surgical resection with curative intent at the Fourth Hospital of Hebei Medical University, China. Eligible patients will be approached consecutively during the recruitment period, before postoperative pathological response is known. Routinely collected primary tumor and regional lymph node specimens will be evaluated. DeepTRG will operate in silent mode, with its outputs withheld from routine reporting pathologists and treating clinicians. Technical failures and unassessable cases will be retained in the feasibility analysis.
Descripción
Inclusion Criteria:
- Age 18 years or older.
- Histologically confirmed adenocarcinoma of the stomach or gastroesophageal junction (Siewert type II or III), diagnosed before neoadjuvant treatment.
- Received neoadjuvant anticancer treatment before planned surgical resection.
- Scheduled to undergo surgical resection with curative intent at the Fourth Hospital of Hebei Medical University, with routine pathological examination of the primary tumor site and regional lymph nodes.
- Written informed consent obtained in accordance with the ethics-approved study protocol.
Exclusion Criteria:
- Non-adenocarcinoma malignancies, including squamous cell carcinoma, lymphoma, gastrointestinal stromal tumor, or neuroendocrine carcinoma.
- Surgery for recurrent gastric or gastroesophageal junction cancer.
- Previous inclusion of the patient's tissue or data in DeepTRG model training, grading-rule development, or parameter tuning.
Patients will not be excluded because of a complete pathological response, positive surgical margins, poor-quality or unavailable slides, digitization failure, algorithm failure, or uncertain or unassessable DeepTRG results. Technical limitations identified after enrollment will be recorded and retained in the feasibility analysis. Patients who do not proceed to surgical resection will be documented in the study flow and will not contribute to the specimen-based primary outcome denominator.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Modelos observacionales: COHORT
- Perspectivas temporales: PROSPECTIVE
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Patient-Level Complete Automated Assessment Rate
Periodo de tiempo: Within 14 days after receipt of the surgical specimen by the pathology department.
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Percentage of enrolled patients undergoing surgical resection for whom DeepTRG generates a complete patient-level pathological response assessment within the specified assessment window, without manual correction of AI-generated segmentations, measurements, or grades. A successful assessment must include the final DeepTRG grade and all required primary tumor and regional lymph node outputs, meet prespecified quality criteria, and have no unresolved uncertainty requiring manual adjudication. The AI model, grading rules, required outputs, and quality criteria will be locked before enrollment. The denominator will include all enrolled patients undergoing eligible surgical resection, including those with unavailable or inadequate slides, digitization failures, processing failures, or unassessable or uncertain outputs. These cases will be counted as unsuccessful assessments. The rate will be reported with a 95% confidence interval. |
Within 14 days after receipt of the surgical specimen by the pathology department.
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
- DeepTRG-SV-001
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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