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1456 PATIENT SELECTION FOR ADJUVANT THERAPY OF PROSTATE CANCER 14. Foster, L. S., Jajodia, P.. Fournier, G., Jr., Shinohara, K., Carroll, P. and Narayan, P.: The value of prostate specific antigen and transrectal ultrasound guided biopsy in detecting prostatic fossa recurrences following radical prostatectomy. J. Urol.. 149 1024, 1993. 15. Ferguson. J. K. and Oesterling, J. E.: Patient evaluation of prostate specific antigen that becomes elevated following rad- ical prostatectomy or radiation therapy. Urol. Clin. N. Amer., 21: 677. 1994. 16. Trapasso. J . G., deKernion. J. B.. Smith, R. B. and Dorey, F.: The incidence and significance of detectable levels of serum pros- tate specific antigen after radical prostatectomy. J. Urol., part 2, 152: 1821, 1994. 17. Epstein, J. I.. Carmichael, M. J.. Pizov. G. and Walsh, P. C.: Influence of capsular penetration on progression following rad- ical prostatectomy: a study of 196 cases with long-term fol- lowup. J. Urol., 150 135, 1993. 18. Norberg, M., Holmberg. L., Wheeler. T. and Magnusson. A.: Five year follow-up after radical prostatectomy for localized pros- tate cancer-a study of the impact of different tumor variables on progression. Scand. J. Urol. Nephrol., 28 391, 1994. 19. DAmico, A. V., Whittington, R., Malkowicz, S. B., Schultz, D., Schnall, M., Tomaszewsh, J. E. and Wein, A,: A multivariate analysis of clinical and pathological factors that predict for prostate specific antigen failure after radical prostatectomy for prostate cancer. J. Urol., 154: 131, 1995. EDITORIAL COMMENT This article contains extremely valuable information for the prac- ticing urologist confronted with an unfavorable pathology report after radical prostatectomy. Setting aside patients with nodal involv- ment it is interesting to note that the incidence of biochemical failure defined by a PSA greater than 0.2 ng./ml. is identical whatever the level of extracapsular extension-roughly 30%, the only difference being the delay at which biochemical relapse occurs: 9 months when the seminal vesicles are invaded versus 30 months in the other cases, indicating that the primary determinant of biochemical relapse may indeed be capsular penetration. When biochemical failure occurs roughly 20%' of untreated pa- tients will experience local or distant progression at 5 years whereas 77% of the patients offered local or systemic chemotherapy will experience a complete response during the same timeframe; this suggests that treatment at biochemical relapse is indeed beneficial, It is possible to define a group of patients who in spite of the presence of extracapsular extension are at low risk of biochemical failure. These patients are characterized by a PSA less than 10 ng./ml. prior to surgery, a specimen Gleason score Of less than 6 and a unique positive margin. The risk of biochemical failure in these patients is identical to what it is observed in patients with pT1-T2 disease, leading to suspect that the patients with pTl-T2 disease who experience biochemical relapse probably have undetected lim- ited capsular penetration. On the contrary, patients with a PSA greater than 10 ng./ml., specimen Gleason score greater than 7 and several positive margins are at high risk of biochemical relapse which will however occur in only 50% of the cases. The question remains open whether all of these patients should be submitted to immediate adjuvant treatment at the risk of over treat- ing 1 patient of 2 or whether adjuvant treatment should be imple- mented only at biochemical relapse. The superiority of immediate versus delayed (at biochemical relapse) therapeutic intervention has yet to be proved. L. BoccowGibod Department of Urology H6pital Bichat Paris. France

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Page 1: EDITORIAL COMMENT

1456 PATIENT SELECTION FOR ADJUVANT THERAPY O F PROSTATE CANCER

14. Foster, L. S., Jajodia, P.. Fournier, G., Jr . , Shinohara, K., Carroll, P. and Narayan, P.: The value of prostate specific antigen and transrectal ultrasound guided biopsy in detecting prostatic fossa recurrences following radical prostatectomy. J. Urol.. 149 1024, 1993.

15. Ferguson. J. K. and Oesterling, J. E.: Patient evaluation of prostate specific antigen that becomes elevated following rad- ical prostatectomy or radiation therapy. Urol. Clin. N. Amer., 21: 677. 1994.

16. Trapasso. J . G., deKernion. J. B.. Smith, R. B. and Dorey, F.: The incidence and significance of detectable levels of serum pros- tate specific antigen after radical prostatectomy. J . Urol., part 2, 152: 1821, 1994.

17. Epstein, J. I . . Carmichael, M. J.. Pizov. G. and Walsh, P. C.: Influence of capsular penetration on progression following rad- ical prostatectomy: a study of 196 cases with long-term fol- lowup. J. Urol., 150 135, 1993.

18. Norberg, M., Holmberg. L., Wheeler. T. and Magnusson. A.: Five year follow-up after radical prostatectomy for localized pros- tate cancer-a study of the impact of different tumor variables on progression. Scand. J. Urol. Nephrol., 2 8 391, 1994.

19. DAmico, A. V., Whittington, R., Malkowicz, S. B., Schultz, D., Schnall, M., Tomaszewsh, J. E. and Wein, A,: A multivariate analysis of clinical and pathological factors tha t predict for prostate specific antigen failure after radical prostatectomy for prostate cancer. J. Urol., 154: 131, 1995.

EDITORIAL COMMENT

This article contains extremely valuable information for the prac- ticing urologist confronted with a n unfavorable pathology report after radical prostatectomy. Setting aside patients with nodal involv- ment it is interesting to note tha t the incidence of biochemical failure defined by a PSA greater than 0.2 ng./ml. is identical whatever the

level of extracapsular extension-roughly 30%, the only difference being the delay at which biochemical relapse occurs: 9 months when the seminal vesicles are invaded versus 30 months in the other cases, indicating tha t the primary determinant of biochemical relapse may indeed be capsular penetration.

When biochemical failure occurs roughly 20%' of untreated pa- tients will experience local or distant progression a t 5 years whereas 77% of the patients offered local or systemic chemotherapy will experience a complete response during the same timeframe; this suggests that treatment a t biochemical relapse is indeed beneficial,

It is possible to define a group of patients who in spite of the presence of extracapsular extension are a t low risk of biochemical failure. These patients are characterized by a PSA less than 10 ng./ml. prior to surgery, a specimen Gleason score Of less than 6 and a unique positive margin. The risk of biochemical failure in these patients is identical to what it is observed in patients with pT1-T2 disease, leading to suspect tha t the patients with pTl-T2 disease who experience biochemical relapse probably have undetected lim- ited capsular penetration. On the contrary, patients with a PSA greater than 10 ng./ml., specimen Gleason score greater than 7 and several positive margins are a t high risk of biochemical relapse which will however occur in only 50% of the cases.

The question remains open whether all of these patients should be submitted to immediate adjuvant treatment at the risk of over treat- ing 1 patient of 2 or whether adjuvant treatment should be imple- mented only at biochemical relapse. The superiority of immediate versus delayed (at biochemical relapse) therapeutic intervention has yet to be proved.

L. BoccowGibod Department of Urology H6pital Bichat Paris. France