Diagnosis of Peritoneal Exfoliative Cytology-positive Gastric Cancer Based on Artificial Intelligence-driven Virtual Biopsy Technology
GC-CY1
1 other identifier
observational
346
1 country
1
Brief Summary
This clinical study aims to develop and evaluate an artificial intelligence (AI)-driven virtual biopsy technology for the diagnosis of gastric cancer with positive peritoneal exfoliative cytology (PEC). Gastric cancer with peritoneal metastasis often presents a challenge for early detection and diagnosis, with traditional diagnostic methods such as imaging and histopathology being limited in sensitivity and specificity. In this study, we propose the use of AI algorithms to analyze non-invasive biomarkers, including transcriptomic profiles and imaging data, to predict the presence of peritoneal exfoliative cytology-positive gastric cancer. Virtual biopsy leverages AI to integrate multiple datasets, providing a comprehensive diagnostic tool that could potentially replace or supplement current invasive diagnostic procedures. By developing this technology, we aim to improve the early diagnosis and monitoring of gastric cancer, particularly in cases with occult peritoneal metastasis, and ultimately enhance patient outcomes through more timely and accurate treatment strategies. The study will involve the collection of clinical samples from gastric cancer patients with suspected peritoneal metastasis. The AI model will be trained on these samples to identify relevant biomarkers for PEC-positive gastric cancer. Clinical validation will be conducted to assess the performance of this AI-driven virtual biopsy system compared to conventional diagnostic methods. This study has the potential to provide a novel, non-invasive diagnostic approach for gastric cancer with peritoneal involvement, offering a significant advancement in the field of early cancer detection and personalized medicine.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2024
CompletedFirst Submitted
Initial submission to the registry
December 28, 2024
CompletedFirst Posted
Study publicly available on registry
January 6, 2025
CompletedJanuary 6, 2025
December 1, 2024
6 months
December 28, 2024
December 28, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Accuracy of AI-Driven Virtual Biopsy in Diagnosing PEC-Positive Gastric Cancer
24 months postoperative follow-up
Interventions
The intervention involves the use of an artificial intelligence (AI)-driven virtual biopsy technology for the non-invasive diagnosis of gastric cancer with positive peritoneal exfoliative cytology (PEC). Unlike traditional biopsy methods, which require invasive procedures to obtain tissue samples, this intervention utilizes AI algorithms to analyze non-invasive biomarkers derived from patient samples such as blood, urine, or peritoneal lavage fluid. The AI model is designed to integrate various data types, including transcriptomic profiling, imaging data, and other biomarkers, to predict the presence of PEC-positive gastric cancer. This technology employs advanced machine learning techniques to identify molecular and cellular features indicative of peritoneal metastasis, providing a diagnostic tool that is potentially more sensitive and less invasive than conventional methods. The intervention is unique in its ability to combine multi-omics data (such as gene expression and imaging.
Eligibility Criteria
The study will involve patients diagnosed with primary gastric cancer who have a clinical suspicion or documented evidence of peritoneal metastasis. Specifically, the study will target individuals with peritoneal exfoliative cytology (PEC)-positive gastric cancer, a condition where peritoneal involvement is suspected based on cytological examination of peritoneal lavage fluid.
You may qualify if:
- Age: Patients aged 18-75 years. Diagnosis of Gastric Cancer: Histologically confirmed diagnosis of primary gastric cancer, with clinical suspicion of peritoneal metastasis (based on imaging or other clinical findings).
- Positive Peritoneal Lavage Cytology (PEC): Patients with suspected PEC-positive gastric cancer, based on previous or current peritoneal lavage cytology results or high clinical suspicion.
- ECOG Performance Status: Eastern Cooperative Oncology Group (ECOG) performance status of 0-2, indicating that the patient is well enough to participate in the study and undergo necessary diagnostic procedures.
- Informed Consent: Ability and willingness to provide informed consent and comply with the study protocol.
You may not qualify if:
- Previous Cancer History: History of other malignancies within the past 5 years, except for non-melanoma skin cancer or in situ cancers.
- Severe Comorbidities: Severe cardiovascular, respiratory, renal, or hepatic disease that would impair the patient's ability to participate in the study or undergo the required diagnostic procedures.
- Pregnancy or Lactation: Pregnant or breastfeeding women, or women planning to become pregnant during the study period.
- Non-Eligible Clinical Conditions: Any condition that, in the opinion of the investigator, could interfere with the patient's participation or compliance with the study protocol, or affect the quality of the data.
- Inability to Provide Samples: Patients who are unable to provide the necessary clinical samples (e.g., blood, urine, or peritoneal lavage fluid) for the AI-driven virtual biopsy analysis.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Qun Zhaolead
Study Sites (1)
the Fourth Hospital of Hebei Medical University
Shijiazhuang, None Selected, 050011, China
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 24 Months
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
December 28, 2024
First Posted
January 6, 2025
Study Start
January 1, 2024
Primary Completion
June 30, 2024
Study Completion
June 30, 2024
Last Updated
January 6, 2025
Record last verified: 2024-12
Data Sharing
- IPD Sharing
- Will not share