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Serum proteomic patterns for detection of prostate cancer

  • Emanuel F. Petricoin*
  • , 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
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

678 Scopus citations

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] ≥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 classifled 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.

Original languageEnglish
Pages (from-to)1576-1578
Number of pages3
JournalJournal of the National Cancer Institute
Volume94
Issue number20
DOIs
StatePublished - 16 Oct 2002
Externally publishedYes

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