Current Age and Race Adjusted Prostate Specific Antigen Threshold Values Delay Diagnosis of High Grade Prostate Cancer
Purpose
Age specific prostate specific antigen ranges have been advocated to increase the predictive value of prostate specific antigen based on increases that occur with aging. We suggest that prostate specific antigen is not a dichotomous biomarker and age specific reference ranges delays the diagnosis of high grade prostate cancer in older and black American men.
Materials and Methods
Using the Prostate Cancer Prevention Trial risk calculator we evaluated the impact of age on the risk of high grade prostate cancer in white and black men. We created a hypothetical population of men by standardizing risk variables, including negative family history, normal digital rectal examination and no history of negative biopsy. Results were compared in the 2 populations using 5-year age increments from ages 55 to 75 years and increasing prostate specific antigen.
Results
Increasing age was associated with a higher risk of high grade prostate cancer in white and black men. The risk of high grade prostate cancer in a black man was twice that in a white man with the same prostate specific antigen at all prostate specific antigen values.
Conclusions
Age specific and race specific prostate specific antigen ranges are flawed. Many patients who would not be considered for biopsy based on these prostate specific antigen ranges are at significant risk for high grade prostate cancer. The risk of high grade prostate cancer in black men is twice that in white men. Risk assessment in black men and older men is necessary to diagnose high grade prostate cancer when treatment can be effective.
Key Words: prostate, prostatic neoplasms, prostate-specific antigen, African Americans, European continental ancestry group
Abbreviations and Acronyms: CAP, prostate cancer, DRE, digital rectal examination, PCPT, Prostate Cancer Prevention Trial, PSA, prostate specific antigen
Supported by National Cancer Institute and Early Detection Research Network Grant U01-CA86402 and a University of Texas Health Sciences Center-San Antonio Institute for Integration of Medicine and Science Mentored Career Development Award (DJP).
PII: S0022-5347(07)01781-8
doi:10.1016/j.juro.2007.07.045
© 2007 American Urological Association. Published by Elsevier Inc. All rights reserved.

