| Literature DB >> 12381711 |
Emanuel F Petricoin1, David K Ornstein, Cloud P Paweletz, Ali Ardekani, Paul S Hackett, Ben A Hitt, Alfredo Velassco, Christian Trucco, Laura Wiegand, Kamillah Wood, Charles B Simone, Peter J Levine, W Marston Linehan, Michael R Emmert-Buck, Seth M Steinberg, Elise C Kohn, Lance A Liotta.
Abstract
Pathologic states within the prostate may be reflected by changes in serum proteomic patterns. To test this hypothesis, we analyzed serum proteomic mass spectra with a bioinformatics tool to reveal the most fit pattern that discriminated the training set of sera of men with a histopathologic diagnosis of prostate cancer (serum prostate-specific antigen [PSA] > or =4 ng/mL) from those men without prostate cancer (serum PSA level <1 ng/mL). Mass spectra of blinded sera (N = 266) from a test set derived from men with prostate cancer or men without prostate cancer were matched against the discriminating pattern revealed by the training set. A predicted diagnosis of benign disease or cancer was rendered based on similarity to the discriminating pattern discovered from the training set. The proteomic pattern correctly predicted 36 (95%, 95% confidence interval [CI] = 82% to 99%) of 38 patients with prostate cancer, while 177 (78%, 95% CI = 72% to 83%) of 228 patients were correctly classified as having benign conditions. For men with marginally elevated PSA levels (4-10 ng/mL; n = 137), the specificity was 71%. If validated in future series, serum proteomic pattern diagnostics may be of value in deciding whether to perform a biopsy on a man with an elevated PSA level.Entities:
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Year: 2002 PMID: 12381711 DOI: 10.1093/jnci/94.20.1576
Source DB: PubMed Journal: J Natl Cancer Inst ISSN: 0027-8874 Impact factor: 13.506