Potters Louis, Morgenstern Carol, Calugaru Emil, Fearn Paul, Jassal Anup, Presser Joseph, Mullen Edward
New York Prostate Institute at South Nassau Communities Hospital, Oceanside, New York 11572, USA.
J Urol. 2008 May;179(5 Suppl):S20-4. doi: 10.1016/j.juro.2008.03.133.
We reviewed the outcomes in men treated with permanent prostate brachytherapy (PPB).
A total of 1,449 consecutive patients with a mean age of 68 years treated with PPB between 1992 and 2000 and mean pretreatment prostate specific antigen (PSA) 10.1 ng/ml were included in this study. Of the patients 55% presented with Gleason 6 tumors and 28% had Gleason 7 disease. A total of 400 patients (27%) were treated with neoadjuvant hormones and 301 (20%) were treated in combination with external radiation plus PPB. Several biochemical freedom from recurrence (BFR) definitions were determined. Statistical analysis consisted of log rank testing, Kaplan-Meier estimates and Cox regression analysis.
Median followup was 82 months with 39 patients at risk at for 144 months. Overall and disease specific survival at 12 years was 81% and 93%, respectively. The 12-year BFR was 81%, 78%, 74% and 77% according to the American Society for Therapeutic Radiology and Oncology (ASTRO), ASTRO-Kattan, ASTRO-Last Call and Houston definitions, respectively. The 12-year ASTRO-Kattan BFR using risk stratification was 89%, 78% and 63% in patients at low, intermediate and high risk, respectively (p = 0.0001). Multivariate analysis identified the dose that 90% of the target volume received (p <0.0001), pretreatment PSA (p = 0.001), Gleason score (p = 0.002), the percent positive core biopsies (p = 0.037), clinical stage (p = 0.689), the addition of hormones (p = 0.655) and the addition of external radiation (p = 0.724) for predicting BFR-ASTRO. Five-year disease specific survival was 44% in patients with a PSA doubling time of less than 12 months vs 88% in those with a PSA doubling time of 12 months or greater (p = 0.0001).
PPB offers acceptable 12-year BFR in patients who present with clinically localized prostate cancer. Implant dosimetry continues as an important predictor for BFR, while the addition of adjuvant therapies such as hormones and external radiation are insignificant. In patients who experience biochemical failure it appears that PSA doubling time is an important predictor of survival.
我们回顾了接受永久性前列腺近距离放射治疗(PPB)的男性患者的治疗结果。
本研究纳入了1992年至2000年间连续接受PPB治疗的1449例患者,平均年龄68岁,治疗前前列腺特异性抗原(PSA)平均为10.1 ng/ml。其中,55%的患者为Gleason 6级肿瘤,28%为Gleason 7级疾病。共有400例患者(27%)接受了新辅助激素治疗,301例(20%)接受了外照射联合PPB治疗。确定了几种生化无复发生存(BFR)的定义。统计分析包括对数秩检验、Kaplan-Meier估计和Cox回归分析。
中位随访时间为82个月,有39例患者随访了144个月。12年时的总生存率和疾病特异性生存率分别为81%和93%。根据美国放射肿瘤学会(ASTRO)、ASTRO-Kattan、ASTRO-Last Call和休斯顿的定义,12年的BFR分别为81%、78%、74%和77%。使用风险分层的12年ASTRO-Kattan BFR在低、中、高风险患者中分别为89%、78%和63%(p = 0.0001)。多因素分析确定了90%靶体积所接受的剂量(p <0.0001)、治疗前PSA(p = 0.001)、Gleason评分(p = 0.002)、阳性穿刺活检百分比(p = 0.037)、临床分期(p = 0.689)、激素添加情况(p = 0.655)和外照射添加情况(p = 0.724)可用于预测BFR-ASTRO。PSA倍增时间小于12个月的患者5年疾病特异性生存率为44%,而PSA倍增时间为12个月或更长的患者为88%(p = 0.0001)。
PPB为临床局限性前列腺癌患者提供了可接受的12年BFR。植入剂量测定仍然是BFR的重要预测指标,而激素和外照射等辅助治疗的添加并无显著影响。在发生生化失败的患者中,PSA倍增时间似乎是生存的重要预测指标。