Prostate Rapid Pre-Validation Set
- Abbreviated Name
- PROS-RAPID
- Lead Investigator
- Sanda, Martin — Emory University
- Coordinating Investigator
- Zheng, Yingye — Fred Hutchinson Cancer Center
- Involved Investigators
-
- — Johns Hopkins University Department of Urology
- Lokshin, Anna — University of Pittsburgh Cancer Institute
- Wagner, Andrew — Beth Israel Deaconess Medical Center
- Haab, Brian — Van Andel Research Institute
- Chan, Daniel — Johns Hopkins Medical Institutions
- Leach, Robin J — University of Texas Health Science Center at San Antonio
- Srivastava, Sudhir — National Cancer Institute
- Diamandis, Eleftherios P. — Mount Sinai Hospital
- Sanda, Martin — Emory University
- Zheng, Yingye — Fred Hutchinson Cancer Center
Abstract
Determine which markers move to validation using the prospectie prostate reference set samples.
Aims
Test candidate prostate markers at various labs using specimens collected and processed in a similar manner.
Analytic Method
N/A
Comments
Specimen Set Depleted
Outcome
hK2, hK4 and hK11 do not distinguish cases from controls. TSP-1 does not seem to distinguish cases from controls. %free PSA has some value: at 0-10% free PSA range for men whose PSA between 4-10 ng/ml, this cutoff point picks up near three folds cases as controls and has since moved on to validation.
Secure Outcome
No secure outcome available.
Publications
- No publications available at this time for this protocol.
Biomarkers
Data Collections
- No data collections available at this time for this protocol.
Team Project
- Start Date
- Feb 1 2006
- Estimated Finish Date
- Feb 10 2007
- Finish Date
- Dec 31 2005
- Protocol ID
- 127
- Protocol Type
- Reference Set
- Fields of Research
-
- Other
- Proteomics
- Collaborative Group
- Prostate and Urologic Cancers Research Group
- Cancer Types
-
- Malignant neoplasm of prostate