Non-Small Cell Lung Carcinoma, Small Cell Lung Carcinoma
Conditions
Brief summary
This pilot clinical trial studies how well bronchoscopy with bronchoalveolar lavage works in identifying biomarkers of response to immune checkpoint inhibitors in patients with non-small cell or small cell lung cancer. Bronchoscopy uses a thin, tube-like instrument inserted through the nose or mouth to view the inside of the trachea, air passages, and lungs. Bronchoalveolar lavage washes out the bronchi and alveoli by flushing with a fluid. Bronchoscopy with bronchoalveolar lavage may make it easier to help determine biomarkers that are more present in some cancers than others that will help determine which individuals have a greater or lesser chance of benefiting from immunotherapy.
Detailed description
PRIMARY OBJECTIVES: I. To discover predictive immune biomarkers of response to immune checkpoint inhibitor therapy in individuals with primary lung cancer. SECONDARY OBJECTIVES: I. To determine biomarkers that may be predictive of treatment related adverse events, specifically pneumonitis. II. To further elucidate lung immunologic microenvironment by performing single cell analysis in addition to mass cytometry (Cytof) on cells of bronchoalveolar lavage. OUTLINE: Patients undergo bronchoscopy with bronchoalveolar lavage over 45 minutes. After completion of study, patients are followed up at 3, 6, 12, and 24 months.
Interventions
Undergo bronchoscopy with bronchoalveolar lavage
OTHERLaboratory Biomarker Analysis
Laboratory Biomarker Analysis
Sponsors
National Cancer Institute (NCI)
Vanderbilt-Ingram Cancer Center
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Confirmed diagnosis of non-small cell lung cancer (NSCLC) or small cell lung cancer (SCLC) * Candidate to undergo immune checkpoint inhibitor (ICI) therapy for SCLC or NSCLC (ICI as any line of chemotherapy is acceptable) as deemed by individual's treating oncologist * Enrollment into this study may occur in tandem with other clinical therapeutics trials occurring at Vanderbilt University Medical Center (VUMC) as long as this trial does not violate protocol or inclusion criteria of that study
Exclusion criteria
* Coagulopathy with international normalized ratio (INR) \> 2.0 or * Coagulopathy with platelets (Plt) \< 10 k * Prior therapy with anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or anti-CTLA-4 antibody (including ipilimumab or any other antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways) * Subjects with an active or recent history of a known or suspected autoimmune disease or recent history of a syndrome that required systemic corticosteroids/immunosuppressive medications * Respiratory failure requiring greater than 6 Lpm supplemental oxygen (O2) by nasal cannula or mechanical ventilation within the past six weeks * Inability to perform informed consent due to any medical or psychiatric condition
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Biomarker response to immune checkpoint inhibitor therapy as measured by Response Evaluation Criteria in Solid Tumors version 1.1 criteria | Up to 24 months |
Countries
United States
Outcome results
None listed