Combination of the preoperative PSA level, biopsy Gleason score, percentage of positive biopsies, and MRI T-stage to predict early PSA failure in men with clinically localized prostate cancer

被引:104
作者
D'Amico, AV
Whittington, R
Malkowicz, SB
Wu, YH
Chen, MH
Art, M
Tomaszewski, JE
Wein, A
机构
[1] Brigham & Womens Hosp, Dept Radiat Oncol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Radiat Oncol, Boston, MA 02115 USA
[3] Hosp Univ Penn, Dept Radiat Oncol, Philadelphia, PA 19104 USA
[4] Hosp Univ Penn, Dept Urol, Philadelphia, PA 19104 USA
[5] Worcester Polytech Inst, Dept Math Sci, Worcester, MA 01609 USA
[6] Hosp Univ Penn, Dept Pathol, Philadelphia, PA 19104 USA
关键词
D O I
10.1016/S0090-4295(99)00479-3
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objectives. Early (2 years or less) prostate-specific antigen (PSA) failure has been shown to predict for distant failure, The independent clinical predictors of time to postoperative PSA failure were used to identify prostate cancer patients at high risk for early PSA failure. Methods. A Cox regression multivariable analysis was used to determine whether additional predictive information was provided by the endorectal coil magnetic resonance imaging (erMRI) T-stage when controlling for the established prognostic factors in predicting the time to postoperative PSA failure in 977 men with palpable (T2) or PSA-detected (T1c) prostate cancer. Results. Preoperative PSA (P = 0.0001), percentage of positive prostate biopsies (P = 0.0001), erMRI T-stage (P = 0.0001), biopsy Gleason score (P = 0.0015), and clinical stage T2c disease (P = 0.004) were independent predictors of time to postoperative PSA failure. Two-year PSA failure rates derived from the Cox regression model and bootstrap estimates of the 95% confidence intervals are presented in nomogram format stratified by the preoperative PSA, percentage of positive prostate biopsies, erMRI T-stage, and the biopsy Gleason score. Conclusions, Patients at high risk for early PSA failure and subsequent distant progression include men with erMRI T3 disease and 3 or more of 6 cores positive for a Gleason score 6 or higher disease when the PSA is more than 10 but not more than 20 ng/mL and any Gleason score when the PSA is more than 20 ng/mL. Men with erMRI T2 disease and 3 or more of 6 cores positive for a Gleason score 8 or higher disease and who have a PSA more than 20 ng/mL are also at high risk. Neoadjuvant therapy trials in these select patients may be justified, UROLOGY 55: 572-577, 2000. (C) 2000, Elsevier Science Inc.
引用
收藏
页码:572 / 577
页数:6
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