Gastric Cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Cases in which HER2_IHC was performed when performing chemotherapy for unresectable advanced/recurrent gastric cancer. 2. Cases in which clinicopathological information can be collected at the time of HER2_IHC measurement.
Exclusion criteria
Exclusion criteria: 1. Cases in which HER2_IHC has not been performed. 2. Patients judged by the principal investigator to be inappropriate as research subjects.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| HER2 positive rate: sample type (biopsy / surgical specimen) and test submission date (Weekday / Weekend) | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. HER2 positive rate among all study subjects 2. Comparison of HER2 positive rate by sample collection date (WD/WE) for different sample types (biopsy/surgical specimen) 3. Comparison of formalin fixation time by sample collection date (WD/WE) 4. Comparison of formalin fixation time by sample type (biopsy/surgical specimen) 5. Comparison of formalin fixation time in the sample type (biopsy/surgical specimen) according to the sample collection date (WD/WE) 6. Comparison of formalin fixation time and HER2 expression rate by sample type (biopsy/surgical specimen) 7. The difference in formalin fixation time (all population/sample type/sample collection date) 8. Comparison of treatment results by HER2 status (positive/negative) (overall survival from the start of chemotherapy, duration of response to trastuzumab combination therapy, and response rate) | — |
Countries
Japan
Contacts
Sapporo City General Hospital Department of Gastroenterology