C34.9
Conditions
Interventions
Group 1: advanced NSCLC with indication for palliative immunotherapy with or without chemotherapy
- determination of the immune cell repertoire in the blood of patients with NSCLC at different points
Sponsors
Krankenhaus Martha-Maria Halle-Dölau
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Patients must be able to give consent themselves - signed consent form - histologically confirmed NSCLC with indication for palliative immunotherapy with or without chemotherapy
Exclusion criteria
Exclusion criteria: - histologically confirmed SCLC - previous immunotherapies
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| progressionfree survival - controll via CT and MRI after 4th cycle of immunotherapy and afterwards every 3 month or if there is clinical indication of progress | — |
Secondary
| Measure | Time frame |
|---|---|
| Overall survival - controll every 3 month - acquiation via Klinisches Krebsregister or genaral practitioner | — |
Countries
Germany
Contacts
Public ContactWolfgang Schütte
Krankenhaus Martha-Maria Halle-Dölau
Outcome results
None listed