Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06035250

AI Prediction of Gastric Cancer Response to Neoadjuvant Chemotherapy

Deep Learning-Based Prediction of Gastric Cancer Response to Neoadjuvant Chemotherapy

Status
Recruiting
Phase
Study type
Observational
Enrollment
200 (estimated)
Sponsor
Chinese Academy of Sciences · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study seeks to develop a deep-learning-based intelligent predictive model for the efficacy of neoadjuvant chemotherapy in gastric cancer patients. By utilizing the patients' CT imaging data, biopsy pathology images, and clinical information, the intelligent model will predict the post-neoadjuvant chemotherapy efficacy and prognosis, offering assistance in personalized treatment decisions for gastric cancer patients.

Detailed description

This study seeks to develop a deep learning model to predict the outcomes of neoadjuvant chemotherapy in patients with gastric cancer. Leveraging participants' CT scans, biopsy pathology images, and clinical profiles, this model aims to forecast the effectiveness of post-neoadjuvant chemotherapy and the subsequent prognosis, thereby aiding in individualized treatment choices for these participants. Data Collection: The investigators will gather data from 1,800 retrospective cases and 200 prospective cases from multiple hospitals. The retrospective data will be divided into training and testing sets to train and validate the model, respectively. The model's performance will subsequently be evaluated using the prospective dataset. Clinical Information: This encompasses the participant's gender, age, tumor markers, staging, type, specific treatment plans, pre and post-treatment lab results, etc. Imaging Data: CT imaging data taken within one month prior to the neoadjuvant chemotherapy, with at least the venous phase CT imaging included. Pathology Data: Pathology images from a gastric tumor biopsy stained with Hematoxylin and Eosin (HE) taken within one month prior to treatment. TRG Grading: Based on the pathology report of the surgical samples using the Ryan TRG grading system. Prognostic Endpoints: The recorded endpoints are a 3-year progression-free survival (PFS) and a 5-year overall survival (OS). All deaths due to non-disease factors are excluded from the prognosis analysis.

Conditions

Interventions

TypeNameDescription
DRUGNeoadjuvant ChemotherapyParticipants in this group are diagnosed with gastric cancer and are scheduled to undergo neoadjuvant chemotherapy as a part of their treatment regimen. The specific chemotherapy drugs, dosages, and schedules will be determined according to established clinical guidelines and the participant's specific condition.

Timeline

Start date
2023-09-10
Primary completion
2024-08-31
Completion
2029-12-31
First posted
2023-09-13
Last updated
2023-09-28

Locations

22 sites across 2 countries: China, Italy

Source: ClinicalTrials.gov record NCT06035250. Inclusion in this directory is not an endorsement.