A Framework for the Identification of Men at Increased Risk for Prostate Cancer
Purpose
We assessed the risk of prostate cancer over time, and the implications for screening strategies and potential risk reduction approaches to provide a framework for clinical use of this approach concordant with the use of prostate specific antigen as a marker of current prostate cancer risk.
Materials and Methods
A comprehensive review of the relevant literature was performed. In this article the phrase risk of/for prostate cancer refers to the risk of developing prostate cancer.
Results
Prostate specific antigen is the single most significant predictive factor for identifying men at increased risk for prostate cancer. A suspicious digital rectal examination, a family history of prostate cancer, the presence of high grade prostatic intraepithelial neoplasia or atypical small acinar proliferation and black ethnicity are also important predictive factors, while larger prostate volume and a previous negative biopsy are negative predictors. For men of screening age (50 to 70 years) a prostate specific antigen of greater than 1.5 ng/ml is a marker for greater than average risk up to 8 years (7.5-times greater risk vs 1.5 ng/ml or less). This prostate specific antigen threshold for a man at above average risk can be modified by the presence of other predictive factors. It should be lower for men with a prostate volume less than 40 cc, black ethnicity or a family history of prostate cancer. For younger men with longer followup a lower prostate specific antigen may be considered.
Conclusions
The risk of prostate cancer can be estimated in individual men primarily using prostate specific antigen, but also using prostate volume, previous biopsy status, family history and ethnicity. Men at increased risk warrant enhanced surveillance and in the future may also be candidates for active risk reduction strategies.
Key Words: prostatic neoplasms, risk factors, prostate-specific antigen, biological markers, early detection of cancer
Abbreviations and Acronyms: %fPSA, percent free PSA, ASAP, atypical small acinar proliferation, BLSA, Baltimore Longitudinal Study of Aging, DRE, digital rectal examination, ERSPC, European Randomized Study of Screening for Prostate Cancer, fPSA, free PSA, HG-PIN, high grade prostatic intraepithelial neoplasia, hK2, human kallikrein 2, PCa, prostate cancer, PSA, prostate specific antigen, PSAD, PSA density, PSAV, PSA velocity, SNP, single nucleotide polymorphism, tPSA, total PSA
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Supported by GlaxoSmithKline.
See Editorial on page 2101.
Editor's Note: This article is the first of 5 published in this issue for which category 1 CME credits can be earned. Instructions for obtaining credits are given with the questions on pages 2538 and 2539.
PII: S0022-5347(09)01742-X
doi:10.1016/j.juro.2009.07.018
© 2009 American Urological Association. Published by Elsevier Inc. All rights reserved.
Refers to article:
- Can Men Reduce the Risk of Prostate Cancer Through Lifestyle Changes? , 16 September 2009

