The primary objective is to identify a panel of plasma and/or serum proteins that differentiates the absence or presence of lung malignancy in samples obtained from subjects enrolled in this IRB/EC approved study with pulmonary nodules.
Blood samples are obtained from those patients undergoing procedures to determine if a lung nodule is benign or cancerous. The data from the study will not be used to guide or influence the treatment of the patients enrolled in this study. There is no change from the normal standard of care that patients receive.
Study Type
OBSERVATIONAL
Enrollment
475
Kaiser Permanente Northern California
San Francisco, California, United States
University of Miami - Sylvester Comprehensive Cancer Center
Miami, Florida, United States
North East Alabama Regional Medical Center
Anniston, Georgia, United States
Incidence rate of Non-Small Cell Lung Cancer
The incidence rate of non-small cell lung cancer in the study population will be correlated to the predictive value of the Sponsor's blood test.
Time frame: 24 months after enrollment
Panel of proteins
The positive and negative predictive value of the test to differentiate between malignancy and inflammatory diseases such as granulomatous disorders.
Time frame: At the end of the study
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Greater Baltimore Medical Center
Baltimore, Maryland, United States
Lahey Hospital & Medical Center
Burlington, Massachusetts, United States
Henry Ford Hospital
Detroit, Michigan, United States
Mayo Clinic
Rochester, Minnesota, United States
University of Cincinnati
Cincinnati, Ohio, United States
Geisinger Medical Center
Danville, Pennsylvania, United States
Cardiopulmonary Research Science and Technology Institute
Dallas, Texas, United States
...and 2 more locations