advanced and recurrent non-small cell lung cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Aged 20<= 2)Histologically or cytologically proven non-small cell lung cancer 3)Stage IIIB without any indications for radiotherapy or stage IV ECOG PS 0 or 1 4)Written informed consent
Exclusion criteria
Exclusion criteria: 1)Patients with serious liver dysfunction or renal dysfunction 2)Pregnant or lactating females 3)Patients with clinically significant psychiatric disease that would interfere with participation in this study 4)Patients with history of previous immune checkpoint inhibitor treatment 5)Patients with history of autoimmune diseases 6)Patients with serious interstitial lung disease or infection
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate correlation between response rates of immune checkpoint inhibitors by PERCIST, by thallium scintigraphy and by RECIST before and 8 weeks after treatment. | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate correlation between response rates of immune checkpoint inhibitors by PERCIST, by thallium scintigraphy and progression free survival and overall survival. | — |
Countries
Japan
Contacts
Kansai Medecal University Hospital Department of Thoracic Oncology