Clinical trial Recruiting at 1 site Observational Ages 18 to 120

Collecting and analyzing lung tissue samples from patients with non-small cell lung cancer

Official title: Molecular Fingerprinting of Lung Cancer

Run by Vanderbilt-Ingram Cancer Center · NCT00897117 · Data updated 2026-11-12

This study is trying to see if analyzing lung tissue samples from patients with non-small cell lung cancer can help predict how their tumors will behave and how well they might do after treatment.

Quick facts

Study typeObservational
Ages18 Years to 120 Years
SexAll
Enrollment4000 (estimated)
SponsorVanderbilt-Ingram Cancer Center
Academic / other
Drugs / interventionsChemotherapy
Locations3 sites (Nashville, Tennessee and 2 other locations)
StatusRecruiting
StartedMay 1, 2001
Main results expectedMay 31, 2031
Study endsMay 31, 2031
Registry record updatedAugust 20, 2026
Trial IDNCT00897117 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are patients diagnosed with resectable stage I or II non-small cell lung cancer who are undergoing surgical resection.

Probably not a fit

Patients who have received chemotherapy or radiotherapy prior to surgery may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This research focuses on collecting and analyzing lung tissue samples from patients undergoing surgery for non-small cell lung cancer. The study aims to develop statistical and computational methods to model the relationships between protein and RNA expression data and clinical outcomes. By examining tissue samples, researchers will identify molecular features that may predict tumor behavior and correlate these findings with clinical data, such as recurrence and survival rates. The study involves multiple centers and utilizes advanced techniques like gene expression analysis and microarray analysis.

Why it matters

Potential benefit: If successful, this study could lead to improved understanding of lung cancer biology and the development of new biomarkers for better patient outcomes.

How similar studies have gone: Other studies have shown success in analyzing tumor tissue samples to identify biomarkers, making this approach promising but not entirely novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion criteria

* Diagnosis of non-small cell lung cancer

  * Clinical stage I and II disease
  * Resectable disease and complete surgical resection planned
* Treated on companion studies at Vanderbilt University, the Veterans Administration hospital, St. Thomas, and Vanderbilt-Ingram Cancer Center Affiliate Network
* Tumor specimen samples must be available at resection

Exclusion criteria

* Chemotherapy before surgery
* Radiotherapy before surgery

Where it's running

  • Vanderbilt-Ingram Cancer Center
    Nashville, Tennessee, United States
    Recruiting
  • Dan Rudy Cancer Center at Saint Thomas Hospital
    Nashville, Tennessee, United States
    Completed
  • Veterans Affairs Medical Center - Nashville
    Nashville, Tennessee, United States
    Suspended

Study contacts

  • Principal investigator: Eric Grogan, MD — Vanderbilt Medical Center
  • Study coordinator: VICC Clinical Trials Information Program
  • Email: cip@vumc.org
  • Phone: 800-811-8480

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.