Development of new approaches for immunotherapy of non-small cell lung cancer
- Conditions
- C34Malignant neoplasm of bronchus and lung
- Registration Number
- DRKS00029641
- Lead Sponsor
- Molekulare PneumologieUniversitätsklinikum Erlangen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- Not specified
Lung tumor patients and control patients with indication for VATS:
Male and female patients 18 years of age and older with a diagnosis of lung cancer who meet the following additional criteria during clinical intervention will be included:
-Completion of a thoracoscopic-guided (VATS = video-assisted thoracic surgery) or open surgical procedure on the lung; and
-performance of a blood sampling procedure and/or
-performing an ultrasound-guided, percutaneous diagnostic or therapeutic puncture of the pleural cavity (effusion, empyema) or a pleural mass and/or
-performance of a bronchoscopy using a flexible or rigid technique (with endobronchial ultrasound: EBUS, if necessary) and/or
-Performing a bronchoscopy with bronchial lavage.
Healthy controls:
-Healthy adults with no past or current tumor diagnosis.
-Non-smokers
Smoker controls:
-Healthy adults with no past or current tumor diagnosis.
-Regular tobacco consumption for at least 1 year.
Lung tumor patients and control patients with indications for VATS:
-Autoimmune diseases
-Severe chron. Diseases
-Other cancer types
Healthy controls and smokers:
-Autoimmune diseases
-Severe chron. Diseases
-Malignant diseases
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Collection of lung tissue, BAL and blood samples. Collection of immunological parameters by flow cytometry, cell culture, ELISA and RNA analysis. Survey of epidemiological parameters by questionnaires.
- Secondary Outcome Measures
Name Time Method