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Retrospective Evaluation of Nivolumab in First-line unresectable advanced or metastatic Gastric Cancer (GC) and Gastroesophageal Junction Cancer (GEJC) : A Non-interventional Study in China

Retrospective Evaluation of Nivolumab in First-line unresectable advanced or metastatic Gastric Cancer (GC) and Gastroesophageal Junction Cancer (GEJC) : A Non-interventional Study in China

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400087604
Enrollment
Unknown
Registered
2024-07-31
Start date
2024-09-05
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Gastric Cancer and Gastroesophageal junction cancer

Interventions

adult patients diagnosed with unresectable advanced or metastatic GC/GEJC and received nivolumab 1L treatment:None

Sponsors

Tongji Hospital, Tongji Medical College ,Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1.Patients with histologically or cytologically confirmed of diagnosis of unresectable advanced or metastatic GC/GEJC; 2.Patients newly received nivolumab as 1L treatment between 15 June 2018 and 30 June 2023; 3.Patients were aged = 18 years at date of first administration of nivolumab; 4.Patients with at least one tumor assessment after index date, patients who have died or stopped treatment with nivolumab due to AE and have not been evaluated will still be included.

Exclusion criteria

Exclusion criteria: 1.Patients with primary malignancies other than unresectable advanced or metastatic GC/GEJC; 2.Patients who participate in an interventional clinical trial in or before 1L nivolumab treatment for advanced/metastatic GC/GEJC; 3.Patients with known HER2 status positive; 4.Patients who investigator deems inappropriate for inclusion, for example clinical data was incomplete;

Design outcomes

Primary

MeasureTime frame
Time to progression (TTP) in 1L;

Secondary

MeasureTime frame
Objective response rate (ORR) in 1L;Clinical characteristics and treatment patterns of patieents who received nioolumab in first-line;Duration of response (DOR) in 1L;Overall survival (OS);All immune-related adverse event (irAE) and adverse events (AEs) that lead to nivolumab discontinuat;

Countries

China

Contacts

Public ContactXianglin Yuan

Tongji Hospital, Tongji Medical College ,Huazhong University of Science and Technology

yuanxianglin@hust.edu.cn+86 27 83663342

Outcome results

None listed

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