Macdonald O Kenneth, Lee R Jeffrey, Snow Greg, Lee Christopher M, Tward Jonathan D, Middleton Anthony W, Middleton George W, Sause William T
Department of Radiation Oncology, LDS Hospital, Salt Lake City, Utah 84143, USA.
Urology. 2007 Feb;69(2):295-9. doi: 10.1016/j.urology.2006.09.058.
To analyze the prostate-specific antigen (PSA) outcome after low-dose adjuvant RT at a single institution, because the role and optimal dose of external beam radiotherapy (RT) after radical prostatectomy for prostate cancer remain controversial.
We retrospectively identified 65 men who had received low-dose adjuvant RT (median 50 Gy) for microscopically positive margins with an undetectable postoperative PSA from 1990 to 2004. Biochemical failure-free survival was the primary endpoint. Biochemical failure was defined as two consecutive PSA increases to greater than 0.2 ng/mL.
At a median follow-up of 5 years, 2 men had developed distant metastasis, 2 had local recurrence, and 2 had died (neither attributable to prostate cancer). Biochemical failure had occurred in 7 men (11%). The 5 and 8-year rate of biochemical failure-free survival was 87%. A greater Gleason score (P = 0.04) and seminal vesicle invasion (P = 0.04) predicted significantly for increased biochemical failure on univariate analysis. No single factor was significant on multivariate analysis. Men with a Gleason score of 7 or less had a 5-year biochemical failure-free survival rate of more than 90%. In contrast, those with a Gleason score of 8 or more had a 50% risk of biochemical failure at 5 years. Acute bowel or bladder toxicity (all grade 2 or less) developed in 25%. Two men developed chronic urethral stricture requiring dilation, and 34 (51%) developed surgery-related toxicity that persisted throughout and after RT.
Low-dose RT is well tolerated and can potentially provide PSA control in men with Gleason score 7 or less disease with positive surgical margins after radical prostatectomy.
分析在单一机构接受低剂量辅助放疗后的前列腺特异性抗原(PSA)结果,因为前列腺癌根治术后外照射放疗(RT)的作用和最佳剂量仍存在争议。
我们回顾性确定了1990年至2004年间65例接受低剂量辅助放疗(中位剂量50 Gy)的男性,这些男性术后PSA不可检测且切缘镜下阳性。生化无复发生存是主要终点。生化失败定义为PSA连续两次升高至大于0.2 ng/mL。
中位随访5年时,2例发生远处转移,2例局部复发,2例死亡(均与前列腺癌无关)。7例男性(11%)发生生化失败。5年和8年生化无复发生存率为87%。在单因素分析中,较高的 Gleason评分(P = 0.04)和精囊侵犯(P = 0.04)显著预测生化失败增加。多因素分析中无单一因素显著。Gleason评分为7分及以下的男性5年生化无复发生存率超过90%。相比之下,Gleason评分为8分及以上的男性5年生化失败风险为50%。25%出现急性肠道或膀胱毒性(均为2级或以下)。2例发生慢性尿道狭窄需要扩张,34例(51%)出现与手术相关的毒性,在放疗期间及放疗后持续存在。
低剂量放疗耐受性良好,对于前列腺癌根治术后切缘阳性、Gleason评分为7分及以下的男性,可能实现PSA控制。