Abstract
Prostate-specific antigen (PSA) is widely used today for the diagnosis and management of men with prostate cancer. It is well known that PSA screening has led to a major stage migration, with most prostate cancers now diagnosed at a localized, curable stage (National Cancer Institute Surveillance Research Program SEER*Stat software, 6.2.4 edn. Available at: http://www.seer.cancer.gov/seerstat). Epidemiologic studies have also shown that prostate cancer mortality rates are lowest in areas where the rates of distant-stage disease are lowest, and distant-stage disease is lowest in areas with the highest PSA utilization (Jemal et al. Cancer Epidemiol Biomarkers Prev 14(3):590–5, 2005). Finally, randomized trials of PSA screening have recently been reported. The European Randomized Study of Screening for Prostate Cancer (ERSPC) and the Goteborg population-based screening trial (including a subset of Swedish ERSPC participants) reported a 21 % and 44 % relative reduction in prostate cancer mortality with screening at 11 and 14 years, respectively (Schroder et al. N Engl J Med Hugosson et al. Lancet Oncol 11(8):725–32, 2010). The US Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial reported no difference in mortality with screening in the overall results (Andriole et al. JNCI 2012; 104: 125-32).
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Loeb, S., Carter, H.B. (2013). PSA Dynamics. In: Jones, J. (eds) Prostate Cancer Diagnosis. Current Clinical Urology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-188-2_4
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DOI: https://doi.org/10.1007/978-1-62703-188-2_4
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