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A multicenter prospective real world study of neoadjuvant chemotherapy efficacy prediction for gastric cancer based on artificial intelligence

A multicenter prospective real world study of neoadjuvant chemotherapy efficacy prediction for gastric cancer based on artificial intelligence

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300068917
Enrollment
Unknown
Registered
2023-03-01
Start date
2023-03-01
Completion date
Unknown
Last updated
2024-09-02

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

Conditions

Gastric cancer

Interventions

group of patients with gastric cancer undergoing preoperative chemotherapy:NA

Sponsors

China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Patient has given informed consent; 2.Aged >= 18 years; 3.Patient has been diagnosed with gastric adenocarcinoma through histopathological biopsy and has available pathological WSI (Whole Slide Imaging); 4.Underwent standardized contrast-enhanced abdominal CT scan prior to neoadjuvant chemotherapy; 5.Diagnosed with locally advanced gastric cancer through contrast-enhanced abdominal CT scan, with infiltration beyond the submucosa and no distant metastasis; 6.No previous gastric surgery; 7.No history of other malignancies before neoadjuvant treatment; 8.No anti-tumor treatment before the contrast-enhanced abdominal CT scan; 9.No mental disorders or cognitive impairment.

Exclusion criteria

Exclusion criteria: 1.Receiving neoadjuvant chemotherapy regimens other than XELOX and SOX; 2.Did not undergo radical surgery after neoadjuvant chemotherapy; 3.Postoperative pathological TRG (Tumor Regression Grade) is unknown; 4.Poor quality of CT images (due to insufficient gastric filling or artifacts) or poor quality of WSI (Whole Slide Imaging); 5.Perioperative death.

Design outcomes

Primary

MeasureTime frame
Tumor regression grade;Efficacy evaluation criteria for solid tumors (RECIST 1.1);

Secondary

MeasureTime frame
overall survival;event-free survival;

Countries

China

Contacts

Public ContactWang Zhenning

The First Hospital of China Medical University

josieon826@sina.cn+86 139 9889 1377

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026