Non-small-cell lung cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Pathologically confirmed advanced non-small cell lung cancer (NSCLC) 2) Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2 3) Patient with evaluable lesion based on RECIST 4) Written informed consent
Exclusion criteria
Exclusion criteria: Other cases attending physician it is determined unsuitable for registration of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| PD-L1 expression status of small samples with each procedure (under rigid bronchoscopy, flexible bronchoscopy, CT & US-guided core-needle, excisional method) | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Total number of tumor cells 2) Comparison of sample size, nunber of tumor cells and PD-L1 expression in BF 1T260 and BF P260F 3) Concordance rate of PD-L1 expression status in biopsy and surgical materials. 4) Efficacy for administration of PD-1 immune checkpoint inhibitor antibody | — |
Countries
Japan
Contacts
St. Marianna University School of Medicine Division of Respiratory Diseases, Department of Internal Medicine