Abbreviated Name

Breast Ref Set App: Zangar (2012)

Lead Investigator

Zangar, Richard (Rick) C. — Pacific Northwest National Laboratory

Coordinating Investigator

Feng, Ziding — Fred Hutchinson Cancer Center

Involved Investigators

• Feng, Ziding — Fred Hutchinson Cancer Center
• Srivastava, Sudhir — National Cancer Institute
• Zangar, Richard (Rick) C. — Pacific Northwest National Laboratory

Abstact

No abstract availalbe.

Aims

Overall, we believe we have identified a promising set of candidate biomarkers for the detection of breast cancer, and our preliminary data justify a validation study using the EDRN Breast Cancer Reference Set. This reference set would be especially valuable for these purposes because: 1. Like our samples, most of the samples for the EDRN Reference Set were collected at the time of biopsy. Thus, this sample set seems particularly well suited for validating our initial study. 2. Given our desire to look at different subtypes of breast cancer, we require a relatively large set of samples to make valid statistical inferences. That is, there are 5 different subtypes of breast cancer, which will effectively reduce the number of samples per group. In this regard, we have previously successfully analyzed a similar number of samples. That is, we previously analyzed nitrotyrosine levels in 24 proteins in 458 plasma samples, and each analysis was done on triplicate ELISA microarray chips [16]. Results from this study demonstrated that we were able to show significant differences between study groups with p values as low as 10-10. Thus, this prior study demonstrates that we can process hundreds of plasma samples and still obtain quality data that is useful for statistical analysis and biological inferences.

Analytic Method

We are proposing a two-stage analysis approach. This approach is based in part on communication with Dr. Margaret Pepe, and her suggestions. Notably, she suggested that in the first phase of the study we should analyze all of the samples except the ones from FCCC. The FCCC samples, which were collected at the time of screening mammography rather than biopsy (as were the rest of the samples), will be analyzed in the second phase, if justified by the first phase. We recognize this is a reasonable and prudent approach, but we would still prefer to simultaneously analyze all 832 plasma samples in the Reference Set, if those samples were made available to us.

Outcome

Our immediate goal is to define a set of biomarkers (composed of circulating plasma proteins) that can be used to distinguish between true and false screens, primarily mammograms. Our preliminary data suggest that different breast cancer subtypes need to be considered when developing this panel. Our long-term goal is to develop a panel of biomarkers that can accurately detect the presence of breast cancer regardless of subtype.

Publications

• No publications available at this time for this protocol.

Biomarkers

• CCL5
• MMP9

Data Collections

• No data collections available at this time for this protocol.

Start Date

Jun 1 2012

Estimated Finish Date

Sep 11 2014

Finish Date

Sep 11 2014

Protocol ID

355

Protocol Type

Reference Set

Field of Research

Proteomics

Collaborative Group

Breast and Gynecologic Cancers Research Group

Cancer Types

• Malignant neoplasm of breast

Phased Status

1