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EXTERNAL BEAM RADIATION THERAPY DOES NOT OFFER LONG-TERM CONTROL OF PROSTATE CANCER - 11/09/11

Doi : 10.1016/S0094-0143(05)70340-2 
Erik T. Goluboff, MD *, Mitchell C. Benson, MD *

Resumen

Prostate cancer is the most common cancer among American men, projected to account for over 240,000 new cases in 1995.25 The advent of prostate-specific antigen (PSA) screening for prostate cancer has led to more cancers being discovered at an early, apparently localized stage.3 Potentially curative treatments for localized prostate cancer include radical prostatectomy and external beam radiation therapy (XRT).1 Another use of serum PSA is to detect early recurrence or persistence of prostate cancer following apparently curative treatment for clinically localized prostate cancer.2, 4, 15 The current definition for cure following radical prostatectomy includes an undetectable serum PSA. A serum PSA of less than 1.5 ng/dL has been suggested as an end point in patients after XRT.2, 4, 8, 9, 10, 11, 15 Whether this is an appropriate end point or a lower PSA is necessary is, to date, unknown.

Cure rates from studies prior to the use of PSA are significantly higher than those being found with the use of this serum marker.7, 19 Using clinical nonbiochemical end points, the efficacies of radical surgery and XRT in the treatment of localized prostate cancer have generally been reported to be relatively equivalent, although this remains very controversial.1, 30 Although desperately needed, no recent controlled studies comparing these two modalities have been completed. The only randomized, controlled trial was reported in 1982 by Paulson et al17 for the Uro-Oncology Research Group. In this study, 97 patients with clinically localized prostate cancer, including normal prostatic acid phosphatase levels, negative bone scans, and negative pelvic lymphadenectomies, were randomized to either radical surgery or XRT. Of the 59 patients randomized to XRT, 52 actually received it and 3 had radical surgery. Of the 47 patients randomized to surgery, 38 received it and 4 had XRT. Although this study has been criticized for many reasons, including this high crossover rate and for data analysis by treatment received and not by the treatment randomized to, the results were quite impressive and the study represents the only randomized data available. The results demonstrated that time to first evidence of treatment failure was significantly shorter (p = 0.037) for those treated by XRT than those treated by surgery. In addition, only four patients in the surgery group had evidence of disease progression in the follow-up period, whereas 17 did in the XRT group.

Recently, Zietman et al30 attempted to compare these two modalities by performing a retrospective literature review with particular attention to long-term follow-up inclusive of PSA and concluded that XRT and radical surgery produced similar results. These authors felt that any differences found (i.e., lower long-term control rates with XRT) could be attributed to differences in patient selection, although it is not clear how this was determined. Adolfsson et al1 reviewed the world's literature to determine the relative efficacies of deferred treatment, radical prostatectomy, and XRT in the treatment of localized prostate cancer. Although this was simply an exhaustive review, not a randomized study, and did not include PSA data, they concluded that 10-year disease-specific survival after surgery was 93%, 83% for deferred therapy and 74% for XRT. Interestingly, mortality due to intercurrent disease was 49.9 per 1000 person-years over the 10-year period in patients treated with deferred therapy, whereas it was 36.3 in those treated with XRT, and only 7 in those treated with surgery, showing significant differences in patient populations between the different treatment groups. This also suggests, however, that those treated with radical surgery had more person-years at risk for prostate cancer progression.

Given the disagreements in the literature concerning the relative efficacies of XRT and surgery in the treatment of clinically localized prostate cancer, we sought to examine the literature with particular attention to posttreatment serum PSA levels. PSA levels are perhaps the most objective and easily obtainable parameter that can be assessed and, in our opinion, the most meaningful surrogate end point.

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Esquema


 Address reprint requests to Mitchell C. Benson, MD, Department of Urology, Columbia-Presbyterian Medical Center, 161 Fort Washington Avenue, New York, NY 10032


© 1996  W. B. Saunders Company. Publicado por Elsevier Masson SAS. Todos los derechos reservados.
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Vol 23 - N° 4

P. 617-621 - novembre 1996 Regresar al número
Artículo precedente Artículo precedente
  • LONG-TERM CONTROL OF PROSTATE CANCER WITH RADIATION : Past, Present, and Future
  • Gerald E. Hanks
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  • SHOULD CRYOSURGERY BE CONSIDERED A THERAPEUTIC OPTION IN LOCALIZED PROSTATE CANCER?
  • John A. Connolly, Katsuto Shinohara, Joseph C. Presti, Peter R. Carroll

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