Predictors of Castration-Resistant Prostate Cancer After Dose-Escalated External Beam Radiotherapy

被引:12
|
作者
Spratt, Daniel E. [1 ]
Zumsteg, Zachary S. [1 ]
Pei, Xin [1 ]
Romesser, Paul B. [1 ]
Yamada, Josh [1 ]
Kollmeier, Marisa A. [1 ]
Woo, Kaitlin [2 ]
Zhang, Zhigang [2 ]
Zelefsky, Michael J. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY 10065 USA
来源
PROSTATE | 2015年 / 75卷 / 02期
关键词
castration resistant prostate cancer; radiotherapy; androgen deprivation therapy; ANDROGEN RECEPTOR GENE; ACQUIRED-RESISTANCE; RADIATION-THERAPY; DEPRIVATION; SURVIVAL; TRIAL; AMPLIFICATION; INTERMITTENT; PROGRESSION; INHIBITORS;
D O I
10.1002/pros.22902
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUNDCastration-resistant prostate cancer (CRPC) is a near uniformly fatal form of prostate cancer; however, information on time to development and predictors for progression to CRPC is limited. We report a detailed longitudinal study for development of CRPC in men initially treated with external beam radiotherapy (EBRT). METHODSDuring 1991-2008, 2,478 patients with clinically localized prostate cancer were treated with dose-escalated EBRT at a single institution. The primary objective was to determine predictors of CRPC among men who failed definitive EBRT and progressed to salvage androgen-deprivation therapy (ADT). CRPC was defined as castrate levels of testosterone (<50ng/dl) with progressive biochemical or radiographic disease. RESULTSFor the entire cohort (n=2,478), the 10-year cumulative incidence rate for developing CRPC was 9.9%. For those that progressed to salvage ADT (n=362), the 7-year cumulative incidence rates for developing CRPC from time of salvage ADT was 33.7%. Amongst this cohort, multivariable analysis demonstrated that PSA doubling-time (continuous; hazard ratio [HR], 0.98 [0.97-0.99], P<0.001), higher Gleason score (HR, 1.96 [1.12-3.43]; P=0.034), and duration of ADT at time of EBRT (continuous; HR, 1.02 [1.01-1.03]; P=0.007) were associated with development of CRPC. CONCLUSIONSThis represents the first report of predictors of CRPC for patients treated with modern dose-escalated EBRT. We demonstrate that among the minority of patients not initially cured after EBRT, those treated with longer-course ADT have higher rates of resistance to the re-introduction of ADT. Future trials will need to test this subgroup with more aggressive or alternative forms of salvage therapies. Prostate 75:175-182, 2015. (c) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:175 / 182
页数:8
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