Optimizing patient selection for dose escalation techniques using the prostate-specific antigen level, biopsy Gleason score, and clinical T-stage

被引:17
作者
D'Amico, AV
Whittington, R
Malkowicz, SB
Schultz, D
Renshaw, AA
Tomaszewski, JE
Richie, JP
Wein, A
机构
[1] Harvard Univ, Sch Med, Joint Ctr Radiat Therapy, Boston, MA 02215 USA
[2] Hosp Univ Penn, Dept Radiat Oncol, Philadelphia, PA 19104 USA
[3] Hosp Univ Penn, Dept Urol, Philadelphia, PA 19104 USA
[4] Hosp Univ Penn, Dept Pathol, Philadelphia, PA 19104 USA
[5] Millersville Univ Pennsylvania, Dept Math, Millersville, PA 17551 USA
[6] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[7] Brigham & Womens Hosp, Dept Urol, Boston, MA 02115 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 1999年 / 45卷 / 05期
关键词
prostate cancer; 3D conformal dose escalation; implant boost; patient selection; prostate-specific antigen;
D O I
10.1016/S0360-3016(99)00303-X
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Ideal candidates for 3D dose escalation conformal radiation or external beam + implant therapy are identified on the basis of the prostate-specific antigen (PSA) level, biopsy Gleason score, and the 1992 American Joint Commission Cancer (AJCC) clinical T-stage. Methods and Materials: The pathologic findings of 1742 men with clinical stage T1c,2 prostate cancer managed with a radical prostatectomy (RP) between 1990 and 1998 were subjected to a logistic regression multivariable analysis. The endpoints examined included pathologic organ-confined (OC), specimen-confined (SC), and margin (M) or seminal vesicle (SV) positive disease. SC disease was defined as extracapsular extension (ECE) with a negative surgical margin. The clinical factors tested included PSA level, biopsy Gleason score, and the 1992 AJCC clinical T-stage. PSA failure-free (bNED) survival was calculated according to the method of Kaplan and Meier. Results: Significant negative predictors of pathologic CC-disease or positive predictors of M+ or SV+ disease included a PSA > 10 ng/ml (p < 0.0001), biopsy Gleason score greater than or equal to 7 (p less than or equal to 0.0004), and greater than or equal to T2b disease (p less than or equal to 0.03). Only biopsy Gleason score 7 (p = 0.0006) and PSA 10-15 ng/ml (p = 0.04) were significant predictors of SC disease. The estimates of 5-year bNED survival were 80%, 62%, and 35% (p < 0.0001) for patients having a low, intermediate, or high likelihood of having Mt or SV+ disease respectively. Conclusions: Patients most likely to derive a survival benefit from the improved local control possible using dose escalation techniques were those who had both a low risk of having occult micrometastatic disease (<25% M+ or SV+) and a reasonable likelihood of remaining disease-free after RP (>50% 5-year bNED). These patients included those having T1c, 2a, PSA > 10-15 ng/ml, and biopsy Gleason less than or equal to 6 or Tie, 2a, 2b, PSA less than or equal to 10 ng/mI, and biopsy Gleason less than or equal to 7 prostate cancer. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:1227 / 1233
页数:7
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