Advanced Lung Adenocarcinoma
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Patients with histologically diagnosed lung adenocarcinoma (2) Patients who received immune checkpoint inhibitors plus chemotherapy for advanced recurrent lung adenocarcinoma (3) Patients whose information can be obtained from the medical record (4) more than 20 years old
Exclusion criteria
Exclusion criteria: (1) Patients who have requested not to participate in this study (2) Patients who are judged ineligible by the principal investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare progression-free survival (PFS) in patients with TTF-1 positive and negative tumors | — |
Secondary
| Measure | Time frame |
|---|---|
| To analyze objective response rate (ORR) PFS and overall survival(OS). To compare ORR and OS in patients with TTF-1 positive and negative tumors. To compare ORR, PFS and OS in patients with TTF-1 positive and negative tumors of Hematoxylin-Eosin Stain-diagnosed lung adenocarcinoma and in patients with TTF-1-diagnosed non-small cell lung cancer (NSCLC) favor adenocarcinoma. To compare ORR, PFS and OS in patients with TTF-1 positive and negative tumors for each chemotherapy regimen. To compare ORR, PFS and OS in patients for each PD-L1 expression. To compare ORR, PFS and OS in patients with TTF-1 positive and negative tumors for each PD-L1 expression. To compare TTF-1 positivity rates by histopathology and compare ORR, PFS and OS in patients with TTF-1 positive and negative tumors. | — |
Countries
Japan
Contacts
Kobe University Graduate School of Medicine division of respiratory medicine, department of Internal medicine,