Impact of race on prostate-specific antigen outcome after radical prostatectomy for clinically localized adenocarcinoma of the prostate

被引:40
作者
Cross, CK
Shultz, D
Malkowicz, SB
Huang, WC
Whittington, R
Tomaszewski, JE
Renshaw, AA
Richie, JP
D'Amico, AV
机构
[1] Brigham & Womens Hosp, Dept Radiat Oncol, Boston, MA 02215 USA
[2] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02215 USA
[3] Brigham & Womens Hosp, Dept Urol, Boston, MA 02215 USA
[4] Dana Farber Canc Inst, Boston, MA 02115 USA
[5] Millersville Univ Pennsylvania, Dept Math, Millersville, PA 17551 USA
[6] Hosp Univ Penn, Dept Urol, Philadelphia, PA 19104 USA
[7] Hosp Univ Penn, Dept Radiat Oncol, Philadelphia, PA 19104 USA
[8] Hosp Univ Penn, Dept Pathol, Philadelphia, PA 19104 USA
关键词
D O I
10.1200/JCO.2002.11.054
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose : To compare prostate-specific antigen (PSA) outcome after radical prostatectomy (RP) for prostate cancer in African-American and white men using previously established risk groups. Patients and Methods: Between 1989 and 2000, 2,036 men (n = 162 African-American men, n = 1,874 white men) underwent RP for clinically localized prostate cancer. Using pretreatment PSA, Gleason score, clinical T stage, and percentage of positive biopsy specimens, patients were stratified into low- and high-risk groups. For each risk group, PSA outcome was estimated using the actuarial method of Kaplan and Meier. Comparisons of PSA outcome between African-American and white men were made using the log-rank test. Results: The median age and PSA level for African-American and white men were 60 and 62 years old and 8.8 and 7.0 ng/mL, respectively. African-Americans had a statistically significant increase in PSA (P =.002), Gleason score (P =.003), clinical T stage (P =.004), and percentage of positive biopsy specimens (P =.04) at presentation. However, there was no statistical difference in the distribution of PSA, clinical T stage, or Gleason score between racial groups in the low- and high-risk groups. The 5-year estimate of PSA outcome was 87% in the low-risk group for all patients (P =.70) and 28% versus 32% in African-American and white patients in the high-risk group (P =.28), respectively. Longer follow-up is required to confirm if these results are maintained at 10 years. Conclusion: Even though African-American men presented at a younger age and with more advanced disease compared with white men with prostate cancer, PSA outcome after RP when controlled for known clinical predictive factors was not statistically different. This study supports earlier screening in African-American men. (C) 2002 by American Society of Clinical Oncology.
引用
收藏
页码:2863 / 2868
页数:6
相关论文
共 49 条
[1]  
ALTSMAN K, 1998, INT J RAD ONCOL B S1, V42, P303
[2]  
*AM CANC SOC, CANC FACTS FIG 2001
[3]  
[Anonymous], UROLOGIC PATHOLOGY
[4]   Population-based study of pelvic lymph node positivity in clinically localized prostate cancer: A study comparing African Americans and whites [J].
Barroso, U ;
Oskanian, P ;
Tefilli, MV ;
Banerjee, M ;
Grignon, D ;
Sakr, W ;
Pontes, JE ;
Powell, IJ .
UROLOGY, 1999, 53 (01) :187-191
[5]  
BEAHRS OH, 1992, AM JOINT COMMITEE CA
[6]   Equivalent racial outcome after conformal radiotherapy for prostate cancer: A single departmental experience [J].
Connell, PP ;
Ignacio, L ;
Haraf, D ;
Awan, AM ;
Halpern, H ;
Abdalla, I ;
Nautiyal, J ;
Jani, AB ;
Weichselbaum, RR ;
Vijayakumar, S .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (01) :54-61
[7]  
CORDER EH, 1995, CANCER EPIDEM BIOMAR, V4, P655
[8]   Biochemical outcome after radical prostatectomy, external beam radiation therapy, or interstitial radiation therapy for clinically localized prostate cancer [J].
D'Amico, AV ;
Whittington, R ;
Malkowicz, SB ;
Schultz, D ;
Blank, K ;
Broderick, GA ;
Tomaszewski, JE ;
Renshaw, AA ;
Kaplan, I ;
Beard, CJ ;
Wein, A .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1998, 280 (11) :969-974
[9]   Clinical utility of the percentage of positive prostate biopsies in defining biochemical outcome after radical prostatectomy for patients with clinically localized prostate cancer [J].
D'Amico, AV ;
Whittington, R ;
Malkowicz, SB ;
Schultz, D ;
Fondurulia, J ;
Chen, MH ;
Tomaszewski, JE ;
Renshaw, AA ;
Wein, A ;
Richie, JP .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (06) :1164-1172
[10]  
Dale W, 1996, PROSTATE, V29, P271, DOI 10.1002/(SICI)1097-0045(199611)29:5<271::AID-PROS1>3.0.CO