Salvage radiotherapy for recurrent prostate cancer after radical prostatectomy

被引:526
作者
Stephenson, AJ
Shariat, SF
Zelefsky, MJ
Kattan, MW
Butler, EB
Teh, BS
Klein, EA
Kupelian, PA
Roehrborn, CG
Pistenmaa, DA
Pacholke, HD
Liauw, SL
Katz, MS
Leibel, SA
Scardino, PT
Slawin, KM
机构
[1] Baylor Coll Med, Scott Dept Urol, Houston, TX 77030 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Urol, Sidney Kimmel Ctr Prostate & Urol Canc, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, New York, NY 10021 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY 10021 USA
[5] Univ Texas, SW Med Ctr, Dept Urol, Dallas, TX USA
[6] Univ Texas, SW Med Ctr, Dept Radiat Oncol, Dallas, TX USA
[7] Cleveland Clin, Dept Urol, Cleveland, OH 44106 USA
[8] Cleveland Clin, Dept Radiat Oncol, Cleveland, OH 44106 USA
[9] Univ Florida, Dept Radiat Oncol, Gainesville, FL USA
[10] Methodist Hosp, Houston, TX 77030 USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2004年 / 291卷 / 11期
关键词
D O I
10.1001/jama.291.11.1325
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Salvage radiotherapy may potentially cure patients with disease recurrence after radical prostatectomy, but previous evidence has suggested that it is ineffective in patients at the highest risk of metastatic disease progression. Objective To delineate patients who may benefit from salvage radiotherapy for prostate cancer recurrence by identifying variables associated with a durable response. Design, Setting, and Patients Retrospective review of a cohort of 501 patients at 5 US academic tertiary referral centers who received salvage radiotherapy between June 1987 and November 2002 for detectable and increasing prostate-specific antigen (PSA) levels after radical prostatectomy. Main Outcome Measure Disease progression after salvage radiotherapy, defined as a serum PSA value greater than or equal to0.1 ng/mL above the postradiotherapy PSA nadir confirmed by a second PSA measurement that was higher than the first by any amount, by,a continued increase in PSA level after treatment, or by the initiation of androgen deprivation therapy after treatment. Results Over a median follow-up of 45 months, 250 patients (50%) experienced disease progression after treatment, 49 (10%) developed distant metastases, 20 (4%) died from prostate cancer, and 21 (4%) died from other or unknown causes. The 4-year progression-free probability (PFP) was 45% (95% confidence interval [01, 40%-50%). By multivariable analysis, predictors of progression were Gleason score of 8 to 10 (hazard ratio [HRI, 2.6; 95% Cl, 1.7-4.1; P<.001), preradiotherapy PSA level greater than 2.0 ng/mL (HR, 2.3; 95% Cl, 1.7-3.2; P<.001), negative surgical margins (HR, 1.9; 95% Cl, 1.4-2.5; P<.001), PSA doubling time (PSADT) of 10 months or less (HR, 1.7; 95% Cl, 1.2-2.2; P=.001), and seminal vesicle invasion (HR, 1.4; 95% Cl, 1.1-1.9; P=.02). Patients with no adverse features had a 4-year PFP of 77% (95% Cl, 64%-91%). When treatment was given for early recurrence (PSA level <= 2.0 ng/mL), patients with Gleason scores of 4 to 7 and a rapid PSADT had a 4-year PFP of 64% (95% Cl, 51%-76%) and of 22% (95% Cl, 6%-38%) when the surgical margins were positive and negative, respectively. Patients with Gleason scores of 8 to 10, positive margins, and receiving early salvage radiotherapy had a 4-year PFP of 81% (95% Cl, 57%-100%) when the PSADT was longer than 10 months and of 37% (95% Cl, 16%-58%) when the PSADT was 10 months or less. Conclusions Gleason score, preradiotherapy PSA level, surgical margins, PSADT, and seminal vesicle invasion are prognostic variables for a durable response to salvage radiotherapy. Selected patients with high-grade disease and/or a rapid PSADT who were previously thought to be destined to develop progressive metastatic disease may achieve a durable response to salvage radiotherapy.
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收藏
页码:1325 / 1332
页数:8
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