The purpose of this study is to assess the treatment-related adverse events and associated healthcare resource use in programmed death ligand 1 (PD-L1) negative individuals diagnosed with advanced/metastatic non-small cell lung cancer (NSCLC) who received first-line therapy
Study Type
OBSERVATIONAL
Enrollment
300
According to the product label
According to the product label
According to the product label
Florida Cancer Specialists & Research Institute
Fleming Island, Florida, United States
Incidence of treatment-related adverse events
Time frame: Baseline
Participant baseline clinical characteristics
Time frame: Baseline
Time to onset of treatment-related adverse events
Time frame: Up to 8 years
Number of treatment-related adverse events resolved
Time frame: Up to 8 years
Number of participants receiving treatment for treatment-related adverse events by drug class
Time frame: Up to 8 years
Number of participants that discontinued immune-oncology therapy due to treatment-related adverse events
Time frame: Up to 8 years
Healthcare Resource Utilization (HCRU) associated with treatment-related adverse event
Time frame: Up to 8 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
According to the product label