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Prognosis and Immunotherapy Efficacy Prediction in Gastric Cancer Using a Multimodal Fusion Model

Prognosis and Immunotherapy Efficacy Prediction in Gastric Cancer Using a Multimodal Fusion Model

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116635
Enrollment
Unknown
Registered
2026-01-13
Start date
2026-01-15
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Gastric cancer

Interventions

Retrospective overall cohort:None
Prospective overall cohort:None

Sponsors

Southern Medical University Southern Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Retrospective cohort 1. Age >= 18 years (); 2. Pathologically or cytologically confirmed gastric cancer, eligible for radical resection, and histologically verified to be predominantly adenocarcinoma (retrospective cohort); 3. Gender: male or female (retrospective cohort); 4. Patients who visited Nanfang Hospital, Southern Medical University between January 2010 and November 2024; met the requirements for regular clinical follow-up of gastric cancer; had no contact with the hospital for at least one year after the follow-up time point; and received complete immunotherapy (including preoperative neoadjuvant immunotherapy) (retrospective cohort); 5. Received complete immunotherapy (including preoperative neoadjuvant immunotherapy) (retrospective cohort); prospective cohort 1. Voluntarily signed the informed consent form; 2. Age >= 18 years; 3. Pathologically or cytologically confirmed gastric cancer, eligible for radical resection, and histologically verified to be predominantly adenocarcinoma; 4. Gender: male or female; 5. Received complete immunotherapy (including preoperative neoadjuvant immunotherapy); 6. Agreed to the use of their own medical data for this research study.

Exclusion criteria

Exclusion criteria: 1.Judged by the researchers as ineligible for participation in this study.

Design outcomes

Primary

MeasureTime frame
Pathological Complete Response;Overall Survival;Major Pathological Response;Area Under the Curve;Progression-Free Survival;

Countries

China

Contacts

Public ContactYanfeng Hu

Southern Medical University Southern Hospital

yfenghu@qq.com+86 20 6278 6329

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026