Open Actively Recruiting

DECAMP 1 PLUS: Prediction of Lung Cancer Using Noninvasive Biomarkers

About

Brief Summary

DECAMP 1 PLUS aims to improve the efficiency of the diagnostic evaluation of patients with indeterminate pulmonary nodules (8-25 mm). Molecular biomarkers for lung cancer diagnosis measured in minimally invasive and non-invasive biospecimens may be able to distinguish between malignant or benign indeterminate pulmonary nodules in high-risk smokers. Ultimately, this study aims to validate molecular as well as clinical and imaging biomarkers of lung cancer in individuals with indeterminate lung nodules.

Study Type
Observational
Phase
N/A

Eligibility

Gender
All
Healthy Volunteers
No
Minimum Age
46 Years
Maximum Age
N/A

Inclusion Criteria:

  • Radiologic diagnosis of solid indeterminate pulmonary nodule (0.8 to 2.5 cm) identified in the past 3 months OR semi-solid (mixed density) nodule with solid component of at least 0.6 cm identified in the past 12 months; must be of appropriate size at enrollment.
  • CT scan completed within 3 months prior to enrollment
  • Able to tolerate all biospecimen collection as required by protocol
  • Able to comply with standard of care follow up visits including clinical exams, diagnostic work-ups, and imaging for approximately three years from enrollment
  • Able to complete the Patient Lung History questionnaire with study staff Arm 1 - Screening
  • Age 55-77 years old
  • Current and former smokers with 30 pack-years or more(and quit less than 15 years ago) Arm 2 - Incidental
  • Age > 45 years old
  • Current and former smokers with 10 pack-years or more(and quit less than 15 years ago)

Exclusion Criteria:

  • History or previous diagnosis of primary lung cancer, metastatic lung cancer, or any other non-lung cancer within 5 years (not including non-melanoma skin cancer)
  • Symptoms of lung cancer (unexplained weight loss 10 lbs or more in 3 months, recent hemoptysis)
  • Diagnosis of pure ground glass opacities for the target lesion on chest CT within the last 12 months (i.e., mixed features on the target lesion and pure ground glass opacity on non-target lesions are acceptable as mentioned above)

Join this Trial

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Study Stats
Protocol No.
20-001577
Category
Oncology
Radiological Sciences
Contact
MEGUMI YOKOMIZO
Location
  • UCLA Santa Monica
  • UCLA Valencia
  • UCLA Westwood
For Providers
NCT No.
NCT04165564
For detailed technical eligibility, visit ClinicalTrials.gov.