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CompletedNCT01580332ISRUSAL01Updated Jul 23, 2014

Non-Invasive Biomarkers For Early Detection Of Lung Cancers

An observational study in Lung Cancer, sponsored by Douglas W. Johnson MD, FACR. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2014-07-23.

Sponsored by Douglas W. Johnson MD, FACR · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
50
Ages
18 Years and older
Sex
All
01

Study summary

Recent studies have shown that low-dose chest CT scans can detect lung cancers in high-risk populations (age >50yo, >30 pack-years of tobacco use), and can lower cancer mortality. Unfortunately, the vast majority of "positive" findings on these CT scans are benign (>95%). Currently, an inordinate amount of expensive follow-up testing is required for these patients to try to prove who among them truly has a cancer.

Several new emerging non-invasive and potentially cheaper tests are now being investigated to help differentiate patients with cancers versus just benign lung nodules. These new tests include a new type of sputum analysis, a breath analysis, a blood test measuring certain tumor markers, a blood test looking for auto-antibodies, and a standard PET/CT scan. Each of these tests have different sensitivity and specificity rates when looking for lung cancer, and it is unclear which test is best.

This study will employ a panel of all 5 of these non-invasive tests on an initial cohort of 50 patients with recently diagnosed lung cancer to try to measure the sensitivity of the tests. A follow-on study will then perform the same panel of tests on 300 lung nodule patients to see which test, or combination of tests, gives the best overall accuracy in terms of predicting who really has lung cancer. It is hoped that the use of such a panel could lead to dramatically decreased need for expensive and morbid invasive testing for this population.

Read the detailed description

The study revolves around specifying the exact signatures and accuracy associated with discriminating between benign and malignant SPNs for each of the biomarkers in the specific high risk cohort under the NLST screening protocol. To help identify and quantify these signatures, we will evaluate specifically the volatile signature in the exhaled breath, the accuracy of LuCED sputum detection, the profile of tumor markers and the specifications of auto-antibodies through immunoassays and Orbitrap technology, and the PET/CT in patients already diagnosed with lung cancer.

02

Conditions studied

  • Lung Cancer

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Keywords

  • biomarkers
  • lung cancer
  • solitary pulmonary nodules
  • SPN
  • breath analysis
  • VOC
  • volatile organic compounds
  • sputum
  • auto-antibodies
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In context

Lung Neoplasms

7,243 studies on the registry are indexed under Lung Neoplasms; 1,557 are open to participants now.

This study's planned enrollment of 50 is below the median of 189 across 1,514 observational studies indexed under Lung Neoplasms.

Browse Lung Neoplasms studies →

Lead sponsor

This is the only study on the registry with Douglas W. Johnson MD, FACR as lead sponsor.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

any patient with newly diagnosed lung cancer (any histology, any stage) who has not yet begun definitive treatment, and who has no prior history of cancer of any type

Inclusion criteria

  • newly diagnosed cancer, prior to treatment

Exclusion criteria

Exclusion Criteria:

  • prior treatment for this cancer
  • a history of any other cancer
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
50 participants (estimated)
Biospecimen retention
Samples with dna
06

Study locations

1 site
  • Baptist Cancer Institute, Baptist Medical Center
    Jacksonville, Florida 32207, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 23, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT01580332
Lead sponsor
Douglas W. Johnson MD, FACR
Responsible party
Douglas W. Johnson MD, FACR (Principal Investigator, Baptist Cancer Institute) — Sponsor-investigator
First posted
Apr 19, 2012
Start date
Jan 2012
Primary completion
Jun 2014
Completion
Jul 2014
Last update
Jul 23, 2014

Study contacts

Douglas W Johnson, MD
principal investigator · Baptist Cancer Institute

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2012. You cannot join it, but the record below documents what was studied.

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