Gutman Sarah, Merrick Gregory S, Butler Wayne M, Wallner Kent E, Allen Zachariah, Galbreath Robert W, Adamovich Edward
Schiffler Cancer Center, Wheeling Hospital, Wheeling, WV 26003, USA.
BJU Int. 2006 Jan;97(1):62-8. doi: 10.1111/j.1464-410X.2006.05887.x.
To determine if the International Prostate Symptom Score (IPSS) before seed implantation, stratified into mild (0-7), moderate (8-19) and severe (>20) categories, predicts brachytherapy-related morbidity in terms of IPSS resolution, catheter dependency and the need for surgical intervention after brachytherapy.
From January 1998 to September 2003, 1034 consecutive patients had permanent interstitial brachytherapy for clinical stage T1b-T3a NXM0 (2002 system) prostate cancer. Of the 1034 patients, 739 (71.5%) presented with an IPSS of 0-7, 287 (27.7%) of 8-19, and eight (0.8%) of > or = 20. The IPSS 8-19 cohort was further stratified into 8-14 (237 men) and 15-19 (50 men) subgroups. The median follow-up was 38.2 months. In all patients, an alpha-blocker was initiated before brachytherapy and continued at least until the IPSS normalized, the latter defined as a return to within 1 point of that before implantation. A median of 21 IPSS questionnaires were obtained per patient. Several clinical, treatment and dosimetric variables were evaluated as predictors of urinary morbidity.
For the entire cohort, the IPSS peaked at a mean of 0.5 months after implantation and resolved at a mean of 1.7 months. At 5 years after brachytherapy, 90.1% of patients at risk (88.8%, 95.5%, and four of eight patients with a pre-implant IPSS of 0-7, 8-19 and > or = 20, respectively) were within the IPSS 0-7 category. Compared to the pre-implant IPSS, 13 patients (8%) were assigned to a higher IPSS severity category. Neither prolonged urinary catheter dependency (>5 days; 16 patients, 1.5%) or transurethral resection of the prostate (TURP, 17 patients, 1.6%) depended on the pre-implant IPSS subgroup. In Cox regression analysis, IPSS resolution was best predicted by pre-implant IPSS, prolonged catheter dependency by patient age, and TURP by any catheter dependency, the maximum IPSS increase and the maximum urethral dose.
The IPSS before implantation predicted the resolution of IPSS after brachytherapy, but did not correlate with substantial urinary morbidity, including catheter dependency or the need for TURP. At 5 years after brachytherapy, 90.1% of patients at risk were assigned to the IPSS 0-7 category.
确定在进行粒子植入前根据国际前列腺症状评分(IPSS)分为轻度(0 - 7分)、中度(8 - 19分)和重度(>20分)类别,能否依据IPSS改善情况、导尿管依赖情况以及近距离放射治疗后手术干预需求来预测近距离放射治疗相关的发病率。
1998年1月至2003年9月,1034例连续患者接受了针对临床分期为T1b - T3a NXM0(2002系统)前列腺癌的永久性组织间近距离放射治疗。在这1034例患者中,739例(71.5%)IPSS为0 - 7分,287例(27.7%)为8 - 19分,8例(0.8%)为≥20分。IPSS为8 - 19分的队列进一步分为8 - 14分(237例男性)和15 - 19分(50例男性)亚组。中位随访时间为38.2个月。所有患者在近距离放射治疗前开始使用α受体阻滞剂,并至少持续至IPSS恢复正常,后者定义为恢复到植入前1分以内。每位患者平均获得21份IPSS问卷。评估了多个临床、治疗和剂量学变量作为泌尿生殖系统发病率的预测因素。
对于整个队列,IPSS在植入后平均0.5个月达到峰值,并在平均1.7个月时恢复正常。近距离放射治疗后5年,处于风险中的患者中90.1%(植入前IPSS为0 - 7分、8 - 19分和≥20分的患者分别为88.8%、95.5%和8例中的4例)处于IPSS 0 - 7分类范围内。与植入前IPSS相比,13例患者(8%)被归类到更高的IPSS严重程度类别。延长的导尿管依赖(>5天;16例患者,1.5%)或经尿道前列腺切除术(TURP,17例患者,1.6%)均不依赖于植入前IPSS亚组。在Cox回归分析中,植入前IPSS对IPSS恢复情况预测最佳,患者年龄对延长的导尿管依赖预测最佳,而TURP则由任何导尿管依赖、IPSS最大增加量和最大尿道剂量预测。
植入前的IPSS可预测近距离放射治疗后IPSS的恢复情况,但与包括导尿管依赖或TURP需求在内的严重泌尿生殖系统发病率无关。近距离放射治疗后5年,90.1%处于风险中的患者被归类到IPSS 0 - 7分类范围内。