4 results on '"Oesterling, Joseph E."'
Search Results
2. Incidence of prostate cancer diagnosis in the eras before and after serum prostate-specific antigen testing
- Author
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Jacobsen, Steven J., Katusic, Slavica K., Bergstralh, Erik J., Oesterling, Joseph E., Ohrt, Del, Klee, George G., Chute, Christopher G., and Lieber, Michael M.
- Subjects
Prostate-specific antigen ,Prostate cancer -- Demographic aspects - Abstract
The increase in the incidence of prostate cancer in the late 1980s and early 1990s may be partly due to the increased use of prostate-specific antigen (PSA) as a diagnostic test. Prostate cancer is the second cause of cancer death in men and is expected to cause 44,000 deaths in 1995. Researchers at the Mayo Clinic in Rochester, MN compared the use of PSA testing in the community beginning in 1987 with the incidence of prostate cancer. The use of PSA testing increased steadily after 1987, especially in men older than 60. The incidence of prostate cancer more than tripled between 1983 and 1992, from 64 cases per 100,000 to 215 per 100,000. The incidence doubled between 1987 and 1988. The incidence of prostate cancer in many age groups began to decline after 1990, indicating that most of the men with prostate cancer have been diagnosed. PSA testing detected prostate cancer earlier, which could lead to higher survival rates., Objective.--To estimate the incidence of prostate cancer in Olmsted County, Minnesota, from 1983 through 1992 to describe the secular changes that have occurred since the introduction of serum prostate-specific antigen (PSA) testing to the community medical practice in 1987. Design.--Population-based, descriptive epidemiological study with ecologic and individual level comparisons over time. Study Setting.--Olmsted County, Minnesota, where the Rochester Epidemiology Project provides passive surveillance of the population for health outcomes. Subjects.--All 511 biopsy-proven incident cases of adenocarcinoma of the prostate diagnosed from 1983 through 1992. The community inpatient and outpatient medical records of all incident cases were reviewed to evaluate the presenting characteristics of men at the time of diagnosis. Results.--The age-adjusted incidence of biopsy-proven prostate cancer increased from 64 per 1 00 000 person-years in 1983 to 215 per 1 00 000 person-years in 1992. The increase occurred primarily between 1987 and 1988 and was predominately for organ-confined tumors. The age-specific incidence increased dramatically in this same period among men aged 50 years and older. Among men aged 70 years and older, however, prostate carcinoma incidence rates declined after 1990 following the initial increase. This decline among older men contrasted with community-based estimates of PSA utilization rates, which demonstrated consistent increases since 1987 to nearly 50% of the older population in 1992. Conclusion.--These results support the premise that the recent increase in prostate cancer is due in part to the increased utilization of serum PSA testing. Further, the increased incidence appears to be a transient phenomenon due to the depletion of previously undiagnosed cases from the prevalence pool. Finally, these data suggest that, in terms of stage at diagnosis, early detection efforts may be effective in identifying more early stage (smaller) cancers. (JAMA. 1995;274:1445-1449)
- Published
- 1995
3. Prostate specific antigen: its role in the diagnosis and staging of prostate cancer
- Author
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Oesterling, Joseph E.
- Subjects
Prostate cancer -- Diagnosis ,Prostate-specific antigen ,Health - Abstract
Prostate specific antigen (PSA) is the most valuable clinical tool available for the diagnosis and staging of prostate cancer. Serum PSA can detect twice as many prostate cancers as digital rectal examination can, and nearly two thirds of these detected tumors are organ-confined and potentially curable. While the diagnostic, routine digital rectal examination has no clinically significant effect on the serum PSA concentration, finasteride therapy causes a 50% lowering of the serum PSA value. The new concepts of PSA velocity, free versus complexed PSA, and age-specific reference ranges all appear to improve further the clinic utility of PSA as a detector of early, potentially curable prostate cancers in men who are most likely to benefit from therapeutic intervention. The serum PSA concentration, when combined with the local clinical stage and histologic grade based on the biopsy specimen, is an excellent predictor of pelvic lymph node status. The probability of pelvic lymph node involvement approaches zero for prostate cancer patients who have the following characteristics: local clinical Stage T1a-T2b disease, primary Gleason grade 1 or 2, and a serum PSA level of 17.1 ng/ml or less; local clinical Stage Tla-T2b disease, primary Gleason grade 3, and a serum PSA level of 8.0 ng/ml or less; local clinical Stage T1a-T2b disease, primary Gleason grade 4 or 5, and a serum PSA level of 4.2 ng/ml or less; local clinical Stage T2c disease, primary Gleason grade 1 or 2, and a serum PSA level of 4.1 ng/ml or less; local clinical Stage T2c disease, primary Gleason grade 3, and a serum PSA level of 2.0 ng/ ml or less; and local clinical Stage T2c disease, primary Gleason grade 4 or 5, and a serum PSA level of 1.0 ng/ ml or less. Staging bilateral pelvic lymph node dissection (open or laparoscopic) can be avoided in these select men. Serum PSA is also an excellent predictor of radionuclide bone scan findings. For patients with newly diagnosed, untreated prostate cancer, no skeletal symptoms, and a serum PSA concentration higher than 10 ng/ml, the probability of a positive bone scan approaches zero. For men who present with this clinical scenario, a staging radionuclide bone scan is not necessary. Using serum PSA to eliminate the staging bilateral pelvic lymph node dissection and radionuclide bone scan in select patients can result in significant economic savings to the health care system. Cancer 1995,75:1795-804.
- Published
- 1995
4. PSA screening and prostate cancer incidence
- Author
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Rhoads, George G., Mills, Orlando F., Berman, Jules J., Moore, G. William, Alonsozana, Edgar L.C., Brown, Lawrence A., Jacobsen, Steven J., Katusic, Slavica K., Bergstralh, Erik J., Klee, George G., Chute, Christopher G., Lieber, Michael M., and Oesterling, Joseph E.
- Subjects
Prostate cancer -- Demographic aspects ,Prostate-specific antigen - Published
- 1996
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