Development of a Predictive Model for Gastric Cancer Peritoneal Metastasis and Cachexia Using BUB1 and Radiopathomics Data With Deep Learning
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 500
- 主要终点
- Predictive Accuracy of the BUB1-Integrated Deep Learning Model for Gastric Cancer Peritoneal Metastasis and Cachexia
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 75 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •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.
排除标准
- •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.
结局指标
主要结局
Predictive Accuracy of the BUB1-Integrated Deep Learning Model for Gastric Cancer Peritoneal Metastasis and Cachexia
时间窗: 12 months for model training, validation, and initial clinical application
次要结局
未报告次要终点
研究者
Qun Zhao
Professor
Hebei Medical University
