Prostate Cancer Screening: What We Know and What We Need To Know

  1. Barnett S. Kramer, MD, MPH;
  2. Martin L. Brown, PhD;
  3. Philip C. Prorok, PhD;
  4. Arnold L. Potosky, MHS; and
  5. John K. Gohagan, PhD
  1. From the Division of Cancer Prevention and Control, National Cancer Institute, Bethesda, Maryland. Acknowledgments: The authors thank Drs. Paul Schellhammer (urology), Ian Thompson (urology), Donald Henson (pathology), and Peter Greenwald (public health) for the critical review and comments on the manuscript.

    Abstract

    Objective: To critically evaluate the evidence for recommending the screening of asymptomatic men for prostate cancer with a blood test to detect a prostate-specific antigen (PSA).

    Data Sources: Relevant articles on screening for prostate cancer were identified from MEDLINE searches, from the authors' files, and from the bibliographies of identified articles.

    Study Selection: In the absence of controlled prospective trials, the studies are primarily retrospective and contain information about the sensitivity, specificity, and predictive values of tests used to screen for prostate cancer; the natural history of untreated prostate cancer; the morbidity, mortality, and costs of definitive treatment; and reviews of screening study biases.

    Data Extraction: Potential treatment-related mortality and costs that could be incurred by screening were estimated using defined assumptions.

    Results: Although screening for prostate cancer has the potential to save lives, because of possible over-diagnosis, screening and subsequent therapy could actually have a net unfavorable effect on mortality or quality of life or both. Given the performance characteristics of the test, widespread screening efforts would probably cost billions of dollars.

    Conclusions: The net benefit from widespread screening is unclear. A randomized prospective study of the effect of screening on prostate cancer mortality has therefore been initiated by the National Cancer Institute.

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