Non-small cell lung cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Age 20 or over. 2) Patients with pathologically confirmed advanced non-small cell lung cancer (NSCLC), and indication of PD-1 immune checkpoint inhibitors (nivolumab or pembrolizumab). 3) Written informed consent.
Exclusion criteria
Exclusion criteria: 1) Patients with metallic device in their body. 2) Patients with claustrophobia. 3) Pregnant or lactating woman. 4) Other cases attending physician it is determined unsuitable for registration of the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage change in FLT accumulation in lymphoid tissues (spleen and bone marrow) before and after PD-1 inhibitor treatment and tumor response to PD-1 inhibitor treatment | — |
Secondary
| Measure | Time frame |
|---|---|
| Relationship between FLT accumulation and patient background (gender, age, height, weight, BMI, smoking history, comorbidities, previous treatment), blood test data and its rate of change (white blood cell count, neutrophil count, lymphocyte count, red blood cell count, hemoglobin, platelet count, RDW, CRP, T.bil, AST, ALT, LDH, BUN, Cr, albumin, tumor markers). Percentage change in FLT accumulation in lymphoid tissue before and after PD-1 inhibitor treatment and its association with progression-free survival and overall survival for PD-1 antibody treatment. | — |
Countries
Japan
Contacts
Faculty of Medical Sciences, University of Fukui Third Department of Internal Medicine