Validation of Molecular Biomarkers for the Early Detection of Lung Cancer in the setting of Indeterminate Pulmonary Nodules (Lung Team Project #2)
- Abbreviated Name
- LTP2
- Lead Investigator
- Lenburg, Marc — Boston University
- Coordinating Investigator
- Feng, Ziding — Fred Hutchinson Cancer Center
- Involved Investigators
-
- Feng, Ziding — Fred Hutchinson Cancer Center
- Herman, James — University of Pittsburgh School of Medicine
- Huflejt, Margaret E. — New York University School of Medicine
- Crichton, Dan — NASA Jet Propulsion Laboratory
- Schabath, Matthew — H. Lee Moffitt Cancer Center & Research Institute, Inc.
- Stass, Sanford — University of Maryland School of Medicine
- Lenburg, Marc — Boston University
- Grogan, Eric — Vanderbilt -Ingram Cancer Center
- Willey, James — University of Toledo College of Medicine
- Sidransky, David — Johns Hopkins University
- Vuskovic, Marko — San Diego State University
- Pass, Harvey Ira — New York University School of Medicine
- Lamb, Carla — Lahey Hospital and Medical Center
- Spira, Avrum — Boston University
- Diaz-Mayoral, Norma — Frederick National Laboratory for Cancer Research
- Srivastava, Sudhir — National Cancer Institute
- Dubinett, Steve — University of California Los Angeles
- Rom, William — New York University School of Medicine
Abstract
To characterize intra or within subject reproducibility and variability To characterize inter or across subject variability by adenoma phenotype (normal vs. adenoma) To evaluate biomarker expression in relation to long term adenoma recurrence
Aims
3.1.1 Aim 1 Establish a cohort (n=200) of current and former smokers with indeterminate pulmonary nodules (7mm-25mm) on whom clinical, radiographic and biospecimen repositories are developed and who are followed prospectively until final diagnosis. 3.1.2 Aim 2 Validate the diagnostic accuracy of existing molecular biomarkers in the airway and blood to detect lung cancer in this clinical cohort.
Analytic Method
Airway gene-expression biomarker (BU) Airway protein biomarker (VU): LC-MRM-MS analyses Serum glycan biomarker (NYU): Plasma promoter methylation biomarker (JHU): Serum cytokines biomarker (UCLA): Serum/Plasma miRNA biomarker (OSU): Plasma miRNA biomarker (UMD):
Outcome
To characterize intra or within subject reproducibility and variability To characterize inter or across subject variability by adenoma phenotype (normal vs. adenoma) To evaluate biomarker expression in relation to long term adenoma recurrence
Publications
- No publications available at this time for this protocol.
Biomarkers
- Bronchial proteomic biomarkers (50)
- CDO1 methylation loci
- CEA (by CBSI from serum)
- CYFRA 21.1 (by CBSI from serum)
- Gene-expression profile (RNA and DNA from nasal and bronchial brushings)
- HE4 (by CBSI from serum)
- HOXA7 methylation loci
- LCP-CNN model (CT-images)
- LFAMB (5 loci in three gene regions of RNA and DNA from nasal and bronchial brushings)
- miRNA profile (plasma)
- NanoString Panel (539 gene-expression probes)
- Radiomic signature (CT-images)
- Serum based quantitation of CYFRA 21.1, CEA and HE4
- SOX17 methylation loci
- TAC1 methylation loci
Data Collections
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Team Project
- Start Date
- Mar 8 2012
- Estimated Finish Date
- Mar 7 2015
- Protocol ID
- 354
- Protocol Type
- Validation
- Fields of Research
-
- Genomics
- Proteomics
- Collaborative Group
- Lung and Upper Aerodigestive Cancers Research Group
- Cancer Types
-
- Malignant neoplasm of bronchus and lung
- Phased Status
- 2