PREDICTING THE RISK OF LYMPH-NODE INVOLVEMENT USING THE PRETREATMENT PROSTATE-SPECIFIC ANTIGEN AND GLEASON SCORE IN MEN WITH CLINICALLY LOCALIZED PROSTATE-CANCER

Citation
M. Roach et al., PREDICTING THE RISK OF LYMPH-NODE INVOLVEMENT USING THE PRETREATMENT PROSTATE-SPECIFIC ANTIGEN AND GLEASON SCORE IN MEN WITH CLINICALLY LOCALIZED PROSTATE-CANCER, International journal of radiation oncology, biology, physics, 28(1), 1994, pp. 33-37
Citations number
32
Categorie Soggetti
Oncology,"Radiology,Nuclear Medicine & Medical Imaging
ISSN journal
03603016
Volume
28
Issue
1
Year of publication
1994
Pages
33 - 37
Database
ISI
SICI code
0360-3016(1994)28:1<33:PTROLI>2.0.ZU;2-K
Abstract
Purpose: To evaluate the predictive value of an empirically derived eq uation for identifying patients with clinically localized prostate can cer at low and high risk for harboring occult lymph node metastasis. M ethods and Materials: A simple equation for estimating the risk of pos itive lymph nodes was empirically derived from a nomogram published by Partin ef al. demonstrating the value of combining the pre-treatment prostate specific antigen and Gleason Score in predicting the risk of lymph node metastasis for patients with clinically localized prostate cancer. The risk of positive nodes (N+) was calculated using the equat ion; N+ = 2/3(PSA) + (GS - 6) x 10, where PSA and GS are the pre-treat ment prostate specific antigen and Gleason Score respectively, and the calculated risk is constrained between 0-65% for a PSA less than or e qual to 40 ng/ml (as in the nomogram). To test the general applicabili ty of this equation, we reviewed the pathologic features of 282 of our patients who had undergone a radical prostatectomy. Results: Based on 212 patients for whom the pre-operative prostate specific antigen's a nd Gleason Scores were available, we identified 145 patients with a ca lculated risk of positive nodes of < 15%, (low risk group) and 67 pati ents with a calculated risk as greater than or equal to 15% (high risk group). The observed incidence of positive nodes, was 6% and 40% amon g the low and high risk groups respectively (p < 0.001). When used alo ne neither clinical stage, pretreatment prostate specific antigen nor the pre-treatment Gleason Score was as useful in identifying the large st low and high risk groups. Conclusion: Using the equation described we confirmed the general applicability of the nomogram reported by Par tin ef al. and identified patients at low and high risk for lymph node involvement. Based on these data we have adopted a policy of omitting whole pelvic irradiation in patients identified as low risk.