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Clinical Study on the Construction and Application of an Intelligent Agent for Gastric Cancer Disease Monitoring Based on ctDNA and Pathological Intelligent Multimodal Data Fusion

Clinical Study on the Construction and Application of an Intelligent Agent for Gastric Cancer Disease Monitoring Based on ctDNA and Pathological Intelligent Multimodal Data Fusion

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600124603
Enrollment
Unknown
Registered
2026-05-14
Start date
2026-05-15
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Gastric Cancer Disease

Interventions

Gold Standard:Tumor Regression Grade

Sponsors

Beijing Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients clinically diagnosed with stage II–IVa gastric adenocarcinoma and adenocarcinoma of the esophagogastric junction (Siewert II/III), confirmed by pathological tissue biopsy; 2. Aged 18–75 years, Eastern Cooperative Oncology Group (ECOG) performance status 0–1; 3. Expected survival >=12 months; 4. No pleural, abdominal, or pelvic effusion, and abdominal-pelvic CT confirms no metastasis to the peritoneum, liver, or other distant organs; 5. Voluntarily willing to sign the informed consent form, demonstrating good compliance and cooperation for follow-up; 6. Intended to receive neoadjuvant drug therapy and undergo radical surgical resection.

Exclusion criteria

Exclusion criteria: 1. Pregnant or breastfeeding women; 2. Those who have received anti-tumor treatment within the past five years; 3. Postoperative pathology indicates positive margins; 4. History of other malignant tumors within the past five years; 5. Uncontrolled pleural effusion, pericardial effusion, or ascites; 6. Severe uncontrolled concurrent infection or other severe uncontrolled comorbidities or diseases that make the subject unfit to participate in the study, or any serious medical disorder that may affect the safety of the subject; 7. Patients requiring emergency surgery, or with complications such as bleeding or obstruction caused by gastric cancer; 8. Clinically severe heart disease or pulmonary dysfunction; 9. Refusal to provide blood or tissue samples; 10. Unable or considered unsuitable for continuing the study due to ethical or medical reasons; 11. Other conditions considered likely to affect patient safety or trial compliance.

Design outcomes

Primary

MeasureTime frame
Tumor Regression Grade;Disease-free survival;AI-powered pathological data;Accuracy;Specificity;

Secondary

MeasureTime frame
ctDNA Dynamic;Gastric Cancer Disease Monitoring Intelligent Agent;

Countries

China

Contacts

Public ContactXin Ji

Beijing Cancer Hospital

jixin41204@bjmu.edu.cn+86 10 8819 6970

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026