Time to prostate specific antigen recurrence after radical prostatectomy and risk of prostate cancer specific mortality

被引:97
作者
Freedland, Stephen J.
Humphreys, Elizabeth B.
Mangold, Leslie A.
Eisenberger, Mario
Partin, Alan W.
机构
[1] James Buchanan Brady Urol Inst, Dept Urol, Baltimore, MD USA
[2] James Buchanan Brady Urol Inst, Dept Oncol, Baltimore, MD USA
关键词
prostate; prostatic neoplasms; prostatectomy; prostate-specific antigen; mortality;
D O I
10.1016/j.juro.2006.06.017
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
Purpose: In patients treated with radical prostatectomy who have biochemical recurrence we have previously reported that time from surgery to biochemical recurrence and postoperative prostate specific antigen doubling time are significantly related to the risk of prostate cancer death. We performed a more thorough examination of the association of time from surgery to biochemical recurrence and the risk of prostate cancer death. Materials and Methods: We retrospectively studied the records of 379 patients treated with radical prostatectomy between 1982 and 2000 who had had biochemical recurrence. We examined the association of time from surgery to prostate specific antigen recurrence and prostate specific antigen doubling time, and the risk of prostate cancer death using the Spearman correlation and Cox proportional hazards regression, respectively. Results: Longer time from surgery to prostate specific antigen recurrence was associated with a slower prostate specific antigen doubling time (Spearman r = 0.36, p < 0.001) and a decreased risk of prostate cancer death (RR 0.76, 95% CI 0.66 to 0.88, p < 0.001). The 15-year actuarial prostate cancer specific survival rate after biochemical recurrence in patients with recurrence at 3 years or less was 41% (95% CI 29 to 53) compared to 87% (95% CI 75 to 93) in patients with recurrence more than 3 years after radical prostatectomy. On multivariate analysis a shorter time from surgery to prostate specific antigen recurrence was associated with an increased risk of prostate cancer death (3 or less vs more than 3 years, RR 2.70, 95% CI 1.37 to 5.31, p = 0.004). Conclusions: Earlier prostate specific antigen recurrence is associated with an increased risk of prostate cancer death. These data suggest that perhaps time to prostate specific antigen recurrence may be a reasonable intermediate end point in patients treated with radical prostatectomy, although this must be validated in other studies.
引用
收藏
页码:1404 / 1408
页数:5
相关论文
共 14 条
[1]   Validation of increasing prostate specific antigen as a predictor of prostate cancer death after treatment of localized prostate cancer with surgery or radiation [J].
Albertsen, PC ;
Hanley, JA ;
Penson, DF ;
Fine, J .
JOURNAL OF UROLOGY, 2004, 171 (06) :2221-2225
[2]   Defining prostate specific antigen progression after radical prostatectomy: What is the most appropriate cut point? [J].
Amling, CL ;
Bergstralh, EJ ;
Blute, ML ;
Slezak, JM ;
Zincke, H .
JOURNAL OF UROLOGY, 2001, 165 (04) :1146-1151
[3]   Early versus late hormonal therapy: Debating the issues [J].
Crawford, ED .
UROLOGY, 2003, 61 (2A) :8-13
[4]   Surrogate end point for prostate cancer-specific mortality after radical prostatectomy or radiation therapy [J].
D'Amico, AV ;
Moul, JW ;
Carroll, PR ;
Sun, L ;
Lubeck, D ;
Chen, MH .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (18) :1376-1383
[5]   Risk of prostate cancer-specific mortality following biochemical recurrence after radical prostatectomy [J].
Freedland, SJ ;
Humphreys, EB ;
Mangold, LA ;
Eisenberger, M ;
Dorey, FJ ;
Walsh, PC ;
Partin, AW .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2005, 294 (04) :433-439
[6]   Defining the ideal cutpoint for determining PSA recurrence after radical prostatectomy [J].
Freedland, SJ ;
Sutter, ME ;
Dorey, F ;
Aronson, WJ .
UROLOGY, 2003, 61 (02) :365-369
[7]   A randomised comparison of bicalutamide ('Casodex') 150 mg versus placebo as immediate therapy either alone or as adjuvant to standard care for early non-metastatic prostate cancer - First report from the Scandinavian Prostatic Cancer Group Study No. 6 [J].
Iversen, P ;
Tammela, TLJ ;
Vaage, S ;
Lukkarinen, O ;
Lodding, P ;
Bull-Njaa, T ;
Viitanen, J ;
Hoisaeter, P ;
Lundmo, P ;
Rasmussen, E ;
Johansson, JE ;
Persson, BE ;
Carroll, K .
EUROPEAN UROLOGY, 2002, 42 (03) :204-211
[8]   Immediate hormonal therapy compared with observation after radical prostatectomy and pelvic lymphadenectomy in men with node-positive prostate cancer [J].
Messing, EM ;
Manola, J ;
Sarosdy, M ;
Wilding, G ;
Crawford, ED ;
Trump, D .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (24) :1781-1788
[9]   Early versus delayed hormonal therapy for prostate specific antigen only recurrence of prostate cancer after radical prostatectomy [J].
Moul, JW ;
Wu, HY ;
Sun, L ;
McLeod, DG ;
Amling, C ;
Donahue, T ;
Kusuda, L ;
Sexton, W ;
O'Reilly, K ;
Hernandez, J ;
Chung, A ;
Soderdahl, D .
JOURNAL OF UROLOGY, 2004, 171 (03) :1141-1147
[10]   Predictors of metastatic disease in men with biochemical failure following radical prostatectomy [J].
Okotie, OT ;
Aronson, WJ ;
Wieder, JA ;
Liao, Y ;
Dorey, F ;
deKernion, JB ;
Freedland, SJ .
JOURNAL OF UROLOGY, 2004, 171 (06) :2260-2264