Chevli Connor, Narayanan Ramkishen, Rambarran Lisa, Kubicek Gregory, Chevli K Kent, Duff Michael
Cancer Care of Western New York, Cheektowaga, NY, USA.
Cancer Care of Western New York, Cheektowaga, NY, USA ; State University of New York at Buffalo School of Medicine and Biomedical Sciences, Buffalo, NY, USA.
Res Rep Urol. 2013 Jan 14;5:29-37. doi: 10.2147/RRU.S38093. eCollection 2013.
The aim of this study was to describe the effect of pretreatment prostate volume on urinary quality of life after intensity-modulated radiation therapy (IMRT) for clinically localized prostate cancer.
A total of 368 men treated with prostate IMRT (77.4-81 Gy) were stratified into three gland volume groups, ie, <30 g (group 1), 30-60 g (group 2), and >60 g (group 3). Post-IMRT urinary function was evaluated by National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) version 4.0 genitourinary guidelines at one year post-IMRT, and surveyed by the International Prostate Symptom Score (IPSS) before treatment, and then at one month and one year post-IMRT.
Late (one year post-IMRT) CTCAE version 4.0 genitourinary toxicity occurred in 11/368 (3.0%) men, but was not severe (grade ≥ 3); total toxicity was similar between the prostate volume groups (P = 0.86). Continuous prostate volume neither correlated with (P = 0.50) nor predicted late genitourinary toxicity (univariate odds ratio 0.99, 95% confidence interval 0.96-1.02). The total IPSS cohort, group 1 (<30 g) and 2 (30-60 g), showed a similar IPSS trend of elevation from pretreatment baseline to one month post-IMRT (each P < 0.01), then a reduction to baseline at one year (each P < 0.01). Group 3 (>60 g) had the highest pretreatment IPSS, but uniquely showed a better urinary symptom trend than the smaller volume groups, with similar IPSS from baseline to one month post-IMRT (P = 0.88) and improved post-treatment IPSS from baseline at one year (P = 0.003).
Pretreatment prostate volume and initial IPSS scores were not associated with increased late genitourinary toxicity after IMRT in our series. Patients with smaller prostates had an initial increase in urinary symptoms, but returned to baseline at one year. Larger prostate glands (>60 g) had comparatively worse pretreatment symptoms, but at one year showed an overall improvement in IPSS versus baseline.
本研究旨在描述临床局限性前列腺癌调强放射治疗(IMRT)前前列腺体积对泌尿生活质量的影响。
共有368例接受前列腺IMRT(77.4 - 81 Gy)治疗的男性被分为三个腺体体积组,即<30 g(第1组)、30 - 60 g(第2组)和>60 g(第3组)。IMRT后1年,根据美国国立癌症研究所不良事件通用术语标准(CTCAE)第4.0版泌尿生殖系统指南评估IMRT后的泌尿功能,并在治疗前、IMRT后1个月和1年通过国际前列腺症状评分(IPSS)进行调查。
11/368(3.0%)的男性出现晚期(IMRT后1年)CTCAE第4.0版泌尿生殖系统毒性,但不严重(≥3级);前列腺体积组之间的总毒性相似(P = 0.86)。前列腺体积的连续性与晚期泌尿生殖系统毒性既无相关性(P = 0.50)也不能预测晚期泌尿生殖系统毒性(单因素优势比0.99,95%置信区间0.96 - 1.02)。整个IPSS队列、第1组(<30 g)和第2组(30 - 60 g)显示出从治疗前基线到IMRT后1个月IPSS升高的相似趋势(各P < 0.01),然后在1年时降至基线(各P < 0.01)。第3组(>60 g)治疗前IPSS最高,但独特地显示出比小体积组更好的泌尿症状趋势,从基线到IMRT后1个月IPSS相似(P = 0.88),且治疗后1年相对于基线IPSS有所改善(P = 0.003)。
在我们的系列研究中,治疗前前列腺体积和初始IPSS评分与IMRT后晚期泌尿生殖系统毒性增加无关。前列腺较小的患者泌尿症状最初增加,但在1年时恢复到基线。前列腺较大(>60 g)的患者治疗前症状相对更差,但在1年时IPSS相对于基线总体有所改善。