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Development of a Predictive Model for Gastric Cancer Peritoneal Metastasis and Cachexia Using BUB1 and Radiopathomics Data With Deep Learning

Development of a Predictive Model for Gastric Cancer Peritoneal Metastasis and Cachexia Using BUB1 and Radiopathomics Data With Deep Learning

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06858644
Acronym
BUDDLE
Enrollment
500
Registered
2025-03-05
Start date
2025-03-01
Completion date
2027-03-01
Last updated
2025-03-05

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

Conditions

Gastric (Stomach) Cancer

Brief summary

This clinical trial aims to develop a predictive model for gastric cancer (GC) peritoneal metastasis and cachexia by integrating BUB1 gene data with radiological and pathological data using advanced deep learning techniques. The study will focus on utilizing imaging genomics (radiomics) and histopathological data to identify early biomarkers for peritoneal metastasis and cachexia in GC patients. By leveraging deep learning algorithms, the project seeks to improve the accuracy and reliability of predictions, enabling earlier intervention and personalized treatment strategies. The ultimate goal is to enhance clinical decision-making and prognosis prediction in GC patients with peritoneal metastasis and cachexia.

Detailed description

Gastric cancer (GC) is one of the most common and aggressive malignancies, with peritoneal metastasis and cachexia significantly contributing to its poor prognosis. The BUB1 gene has been implicated in chromosomal instability and the progression of GC, but its role in peritoneal metastasis and cachexia remains unclear. This clinical trial aims to explore the potential of integrating BUB1 gene expression with imaging and pathological data to develop a predictive model for GC progression. The study will collect comprehensive data from GC patients, including genomic profiles (BUB1 gene expression), radiological images (CT/MRI scans), and histopathological findings. Advanced radiomics analysis will extract quantitative features from imaging data, while pathological data will be analyzed for relevant histological markers. The combined dataset will be fed into a deep learning model to identify patterns associated with peritoneal metastasis and cachexia, focusing on the identification of early biomarkers. The deep learning model will undergo iterative training and validation using both retrospective and prospective patient data. The primary endpoint of the trial is to assess the model's predictive accuracy for peritoneal metastasis and cachexia development, while secondary endpoints include its potential to inform personalized treatment strategies, improve survival rates, and guide clinical decision-making. This study will also investigate the correlation between BUB1 expression and the radiopathomics features in GC, providing insights into the underlying mechanisms driving peritoneal metastasis and cachexia. The findings aim to establish a robust, clinically applicable predictive tool that can be integrated into current clinical practice for better patient outcomes.

Interventions

DIAGNOSTIC_TESTBUB1-Integrated Deep Learning Model for Gastric Cancer Metastasis and Cachexia Prediction

This intervention utilizes a deep learning model that integrates BUB1 gene expression, radiopathomics (quantitative imaging features), and histopathological data to predict peritoneal metastasis and cachexia in gastric cancer (GC) patients. Unlike traditional approaches, this model combines genomic, imaging, and pathological data to enhance early detection and improve prognostic accuracy. The model aims to identify key patterns in multi-modal data to offer personalized predictions for GC progression. By leveraging artificial intelligence, it seeks to support clinicians in decision-making, improving patient outcomes through earlier interventions and tailored treatments. This approach offers a novel, comprehensive method for predicting GC metastasis and cachexia, providing a unique tool compared to existing interventions.

Sponsors

Qun Zhao
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years

Inclusion criteria

Adults aged 18-75 years diagnosed with gastric cancer (GC) at any stage. Histopathologically confirmed GC with available radiological (CT/MRI) and pathological data (biopsy samples). Patients with or at risk of peritoneal metastasis and/or cachexia, as determined by clinical assessment and imaging. Ability to provide informed consent and comply with study protocols. Willingness to undergo regular follow-up imaging and clinical evaluation for the duration of the study.

Exclusion criteria

Patients with other primary cancers or serious comorbidities (e.g., severe cardiovascular disease, uncontrolled diabetes). Pregnant or breastfeeding women. Patients with contraindications to MRI or CT imaging. Those with insufficient clinical data (e.g., missing radiopathological information) for model training. Patients who are unable or unwilling to comply with the study protocol, including follow-up visits and evaluations.

Design outcomes

Primary

MeasureTime frame
Predictive Accuracy of the BUB1-Integrated Deep Learning Model for Gastric Cancer Peritoneal Metastasis and Cachexia12 months for model training, validation, and initial clinical application

Outcome results

None listed

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