USING PROSTATE-SPECIFIC ANTIGEN TO ELIMINATE THE STAGING RADIONUCLIDE BONE SCAN - 11/09/11
Résumé |
In 1996, an estimated 317,000 new cases of prostate cancer will be diagnosed in the United States, and an estimated 41,000 men will die of this disorder.26 Clearly, cancer of the prostate is an important disease process that deserves the attention of clinicians and researchers alike. Managing prostate cancer in a clinically efficient manner ultimately will allow improved economic conditions that will serve our community. For this reason, efforts have been made to improve many facets of the management of prostate cancer, including staging. Scientists continue to seek molecular, clinical, and radiographic aids to develop a refined, low-cost, and precise staging system.
Traditionally, the standard initial staging evaluation for the newly diagnosed prostate cancer patient included the digital rectal examination (DRE), serum prostatic acid phosphatase (PAP) measurement, a chest radiograph, and a radionuclide bone scan. In more recent years, important clinical data15 , 20 , 23 , 24 , 29 , 30 have permitted prostate-specific antigen (PSA) essentially to replace PAP as a staging tumor marker. Under specific clinical situations, PSA also may replace other staging modalities, such as the radionuclide bone scan.
This article discusses the rationale and methods for using the serum PSA level to eliminate the radionuclide bone scan as a staging tool in many patients with newly diagnosed prostate cancer. Specific clinical scenarios in which this elimination is applicable are outlined and reviewed in the discussion that follows.
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Address reprint requests to Joseph E. Oesterling, MD, The Michigan Prostate Institute, The University of Michigan, 1500 East Medical Center Drive, Ann Arbor, MI 48109–0330 |
Vol 24 - N° 2
P. 389-394 - mai 1997 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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