Acute urinary morbidity following I-125 interstitial implantation of the prostate gland.

J Desai, R G Stock, N N Stone, C Iannuzzi, J K DeWyngaert
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引用次数: 134

Abstract

The objective of this paper was to evaluate the acute urinary morbidity associated with I-125 interstitial implantation of the prostate gland. From 1991-1995, 117 patients underwent ultrasound (U/S)-guided implantation of the prostate gland. Median dose to 90% of the gland (d90) was 14.68 Gy (range = 1.65-21.75 Gy). The patients' urinary symptoms were recorded pre-implantation and at regular intervals after implantation using the International Prostate Symptom Score (IPSS), a self-assessment questionnaire in which patients scored 7 symptoms: incomplete emptying, frequency, intermittency, urgency, weak stream, straining, and nocturia. Median follow-up was 12 months. The natural history of implant-related urinary symptoms was assessed in this manner. In addition, dosimetric factors including U/S prostate volume, total activity, activity per seed, dose volume histogram (DVH) values for dose to gland, and dose area histogram (DAH) values for dose to urethra and bladder were examined for correlation to the severity of each symptom as well as to total IPSS (sum of the individual symptom scores). Total IPSS peaked at 1 month post-implant and gradually returned to approximately baseline at 24 months. Total IPSS directly correlated with total activity and DVH for the prostate. Total IPSS, however, did not correlate with bladder or urethral DAH. With the exception of frequency, individual symptoms did not correlate with dose to gland, bladder, or urethra. Frequency scores did, however, correlate not only with dose to prostate gland but also dose to urethra. The acute urinary side effects of I-125 prostate implantation are transient and peak at 1 month post-implant. The severity of the urinary irritative symptoms developed are closely related to total dose to the gland. Urethral dose appears to affect frequency most significantly. Urinary symptoms, therefore, may be a limiting factor when considering dose escalation with I-125.

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前列腺I-125间质植入后的急性泌尿系统疾病。
本文的目的是评估前列腺I-125间质植入的急性泌尿系统发病率。1991-1995年间,117例患者接受超声引导下的前列腺植入。90%腺体(d90)的中位剂量为14.68 Gy(范围= 1.65-21.75 Gy)。采用国际前列腺症状评分(IPSS)(一种自我评估问卷)记录患者在植入前和植入后定期出现的泌尿系统症状。IPSS评分包括排空不完全、尿频、间歇性、尿急、尿流弱、紧张和夜尿等7种症状。中位随访时间为12个月。以这种方式评估植入物相关泌尿系统症状的自然史。此外,剂量学因素包括前列腺体积U/S、总活度、每粒活度、剂量到腺体的剂量体积直方图(DVH)值、剂量到尿道和膀胱的剂量面积直方图(DAH)值,以检查与每种症状严重程度以及总IPSS(个体症状评分之和)的相关性。总IPSS在植入后1个月达到峰值,并在24个月时逐渐恢复到接近基线的水平。总IPSS与前列腺总活动和DVH直接相关。然而,总IPSS与膀胱或尿道DAH无关。除频率外,个别症状与对腺体、膀胱或尿道的剂量无关。然而,频率评分不仅与前列腺剂量有关,而且与尿道剂量有关。I-125前列腺植入的急性泌尿系统副作用是短暂的,在植入后1个月达到高峰。尿路刺激症状的严重程度与对腺体的总剂量密切相关。尿道剂量对频率的影响最为显著。因此,在考虑I-125剂量增加时,泌尿系统症状可能是一个限制因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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