C34.9
Conditions
Interventions
Group 1: Female lung cancer patients treated with checkpoint inhibitors
Group 2: Male lung cancer patients treated with checkpoint inhibitors
Sponsors
LMU Klinikum
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: written informed consent, NSCLC or SCLC, histological diagnosis, Stage IV
Exclusion criteria
Exclusion criteria: Unwilling to provide clinical history or blood sample
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Response to Treatment (Routine follow up imaging, generally CT, PET-CT or MRI 6-12 weeks after first treatment and at 6-12 week intervals thereafter) | — |
Secondary
| Measure | Time frame |
|---|---|
| Immune Biomarkers | — |
Countries
Germany
Contacts
Public ContactAmanda Tufman
LMU Klinikum, Medzinische Klinik V
Outcome results
None listed