Moreira Daniel M, Howard Lauren E, Sourbeer Katharine N, Amarasekara Hiruni S, Chow Lydia C, Cockrell Dillon C, Hanyok Brian T, Aronson William J, Kane Christopher J, Terris Martha K, Amling Christopher L, Cooperberg Matthew R, Liede Alex, Freedland Stephen J
Department of Urology, Mayo Clinic, Rochester, MN.
Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC; Urology Section, Veterans Affairs Medical Center, Durham, NC.
Urology. 2016 Oct;96:171-176. doi: 10.1016/j.urology.2016.06.011. Epub 2016 Jun 16.
To investigate predictors of time to metastasis among men treated with androgen deprivation therapy for nonmetastatic prostate cancer who developed castration-resistant prostate cancer (CRPC) within the Shared Equal Access Regional Cancer Hospital cohort.
This is a retrospective analysis of 458 nonmetastatic CRPC men. Metastases were detected in routine bone scans or other imaging tests. Predictors of time to metastasis were analyzed using proportional hazards model with CRPC as time zero.
A total of 256 (56%) men were diagnosed with metastatic disease over a median follow-up of 36 months. Metastasis-free survival was 79%, 65%, 52%, 47%, and 41% at 1, 2, 3, 4, and 5 years after CRPC, respectively. In multivariable analysis, Gleason score 8-10 (hazard ratio [HR] = 1.61; P = .026), receiving primary localized treatment (HR = 1.38; P = .028), higher prostate-specific antigen (PSA) levels at CRPC diagnosis (logPSA HR = 1.64; P < .001), and PSA doubling time ≤6 months (HR = 1.42; P = .040) were independently associated with shorter time to metastasis. Race, year of CRPC, age, and time from androgen deprivation therapy to CRPC were not associated with metastasis.
Among nonmetastatic CRPC men, nearly 60% developed metastatic disease during the first 5 years, with most of the metastasis occurring within the first 3 years. Higher Gleason score, receiving primary treatment, higher PSA, and shorter PSA doubling time were independently associated with shorter time to metastasis. Therefore, these variables can be used to stratify patients according to metastasis risk.
在共享平等准入区域癌症医院队列中,研究接受雄激素剥夺治疗的非转移性前列腺癌且发生去势抵抗性前列腺癌(CRPC)的男性患者发生转移时间的预测因素。
这是一项对458例非转移性CRPC男性患者的回顾性分析。通过常规骨扫描或其他影像学检查检测转移情况。以CRPC发生时间为零,使用比例风险模型分析转移时间的预测因素。
在中位随访36个月期间,共有256例(56%)男性被诊断为转移性疾病。CRPC发生后1年、2年、3年、4年和5年的无转移生存率分别为79%、65%、52%、47%和41%。多变量分析显示, Gleason评分8 - 10分(风险比[HR]=1.61;P = 0.026)、接受原发局部治疗(HR = 1.38;P = 0.028)、CRPC诊断时较高的前列腺特异性抗原(PSA)水平(logPSA HR = 1.64;P < 0.001)以及PSA倍增时间≤6个月(HR = 1.42;P = 0.040)与较短的转移时间独立相关。种族、CRPC发生年份、年龄以及从雄激素剥夺治疗到CRPC的时间与转移无关。
在非转移性CRPC男性患者中,近60%在最初5年内发生转移性疾病,且大多数转移发生在最初3年内。较高的Gleason评分、接受原发治疗、较高的PSA水平以及较短的PSA倍增时间与较短的转移时间独立相关。因此,这些变量可用于根据转移风险对患者进行分层。