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Utility of Biomarkers for Early Detection of Malignant Mesothelioma in a High-risk Population

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No involved investigator sites defined.

Quantitative measurement of SMRPs will be done by two-step immunoassay on human serum using enzyme immunoassay technology with colorimetric detection in a standard sandwich ELISA format. Two monoclonal antibodies are used, one for capture and the other for detection. Sera will be sent to the NYU biomarker labor atory and also measured for SMRP in within one month to compare with the levels in found in Chile. Osteopontin and fibulin-3 will be measured in plasma samples, following manufacturer specifications similar to those used for SMRPs. HMGB1 will also be measured by standard ELISA from serum.
Proteomics
Epigenomics
Lung and Upper Aerodigestive Cancers Research Group

A prospective study to evaluate the utility of various biomarkers in the context of an MM Early Detection Program. The study cohort will be composed of workers at a company with known asbestos exposure. Historically, a considerable number of workers at this company have developed MM.

Determine whether serial determination of osteopontin, mesothelin and fibulin-3, and HMGB1 in plasma samples can be used as biomarkers [sic] for early detection of MM in high-risk populations.  Determine the utility of measuring levels of t hese biomarkers in pleural fluid samples from patients who develop pleural effusion.  Determine the utility of these biomarkers for monitoring MM patients undergoing different treatment modalities.  Create a plasma/serum/PAXgene/DNA sample "bank" that can be used for genetic and biomarker studies by researchers at participating institutions or other researchers worldwide.
Assuming 300-375 participants, a 0.5-1.0% per year incidence rate of MM, and three years of follow-up per participant, we project 4-11 incident cases of MM over the course of the study. This sample size will provide insufficient power to build and test models combining multiple markers. The study will have low power but will have the benefits of having a ProBE design with the ability to examine the time course of mark ers and their prognostic ability to detect MM prior to detection via chest CT scan. The performance of the individual markers (SMRP, osteopontin, fibulin-3, and HMGB1) at the time of a chest CT scan will be assessed by ROC curves. Blood measurements taken at a time that there is not a concurrent chest CT scan (e.g., mid-year blood draws without an 17 actionable SMRP level for which there would be no protocol-specified chest CT scan) will not be included in this analysis. The prognostic ability of markers will be assessed by ROC curves using marker values one or two years prior to the time of diagnosis of MM. For each marker, we will produce a plot of the ti me course of the marker for each individual with the time courses for cases of MM highlighted and the time of MM detection indicated, to develop hypotheses about the time course of marker values prior to MM detection, which in turn can be used to develop alternative marker decision rules (e.g ., based on SMRP trajectory) that incorporate longitudinal marker values. This analysis will be exploratory.

There are currently no biomarkers annotated for this protocol.

No datasets are currently associated with this protocol.


2015 EDRN PI Orientation

The New and Continuing EDRN Principal Investigator Orientation will take place January 20–21, 2016 in Bethesda, Maryland.

Announcement 08/26/2015

Thank you to everyone who made the 29th EDRN Steering Committee Meeting a success. The orientation for new and continuing EDRN PIs will be held Wednesday-Thursday, January 20-21, 2016, on the NCI campus. More information will be available later this summer.

Announcement 06/30/2015

A funding opportunity for a new pancreatic cancer initiative, called The Pancreatic Cancer Detection Consortium (U01), has been released. For more information, please go to http://grants.nih.gov /grants/guide/ pa-files/ PAR-15-289.html.