Biochemical Outcome for Hormone‐Naïve Patients with High‐Risk Prostate Cancer Managed with Permanent Interstitial Br achy therapy and Supplemental External‐Beam Radiation

G. Merrick, W. Butler, J. Lief, R. Galbreath, E. Adamovich
{"title":"Biochemical Outcome for Hormone‐Naïve Patients with High‐Risk Prostate Cancer Managed with Permanent Interstitial Br achy therapy and Supplemental External‐Beam Radiation","authors":"G. Merrick, W. Butler, J. Lief, R. Galbreath, E. Adamovich","doi":"10.1097/00130404-200207000-00008","DOIUrl":null,"url":null,"abstract":"PURPOSEThe purpose of this article is to report the 5-year biochemical disease-free outcome for hormone-naive patients with high-risk disease who underwent permanent prostate brachytherapy. Multiple clinical and treatment parameters were also evaluated to determine whether any of these influence biochemical outcome. MATERIALS AND METHODSSixty-six hormone-naïve patients underwent transperineal ultrasound-guided permanent prostate brachytherapy with generous periprostatic margins by use of either 103Pd or 125I for high-risk prostate cancer from April 1995 to October 1999. High-risk patients presented with two or three of the following risk factors: Gleason score ≥ 7, prostate-specific antigen ≥ 10 ng/mL, and clinical stage ≥ T2b, 1997 AJCC. No patient underwent pathological lymph node staging. Only one patient was implanted with monotherapy, whereas 65 patients received supplemental external-beam radiation therapy before a prostate brachytherapy boost. The median patient age was 69 years (range, 50–81 years). No patient was lost to follow-up. The mean follow-up and median follow-up were 53.2 ± 14.9 months and 53.7 months, respectively (range, 19.8–79.7 months). Follow-up was calculated from the day of implantation. Biochemical disease-free survival was defined by the American Society of Therapeutic Radiology and Oncology consensus definition. Clinical parameters evaluated for biochemical disease-free survival included patient age, clinical stage, Gleason score, and pretreatment prostate-specific antigen. Treatment parameters included use of supplemental external-beam radiation therapy and choice of isotope. RESULTSThe 5-year actuarial biochemical disease-free survival rate was 79.9%. In multivariate analysis, preimplantation prostate-specific antigen (P = 0.008) was the only clinical or treatment parameter that predicted for biochemical failure. The mean and median posttreatment prostate-specific antigen levels were 0.13 ± 0.22 ng/mL and < 0.1 ng/mL, respectively. DISCUSSIONAt a median follow-up of 53.7 months, hormone-naive patients with high-risk disease who undergo permanent prostate brachytherapy have a high probability of 5-year biochemical disease-free survival and an apparent plateau on the biochemical disease-free survival curve.","PeriodicalId":22430,"journal":{"name":"The Cancer Journal","volume":"25 1","pages":"322–327"},"PeriodicalIF":0.0000,"publicationDate":"2002-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"25","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Cancer Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/00130404-200207000-00008","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 25

Abstract

PURPOSEThe purpose of this article is to report the 5-year biochemical disease-free outcome for hormone-naive patients with high-risk disease who underwent permanent prostate brachytherapy. Multiple clinical and treatment parameters were also evaluated to determine whether any of these influence biochemical outcome. MATERIALS AND METHODSSixty-six hormone-naïve patients underwent transperineal ultrasound-guided permanent prostate brachytherapy with generous periprostatic margins by use of either 103Pd or 125I for high-risk prostate cancer from April 1995 to October 1999. High-risk patients presented with two or three of the following risk factors: Gleason score ≥ 7, prostate-specific antigen ≥ 10 ng/mL, and clinical stage ≥ T2b, 1997 AJCC. No patient underwent pathological lymph node staging. Only one patient was implanted with monotherapy, whereas 65 patients received supplemental external-beam radiation therapy before a prostate brachytherapy boost. The median patient age was 69 years (range, 50–81 years). No patient was lost to follow-up. The mean follow-up and median follow-up were 53.2 ± 14.9 months and 53.7 months, respectively (range, 19.8–79.7 months). Follow-up was calculated from the day of implantation. Biochemical disease-free survival was defined by the American Society of Therapeutic Radiology and Oncology consensus definition. Clinical parameters evaluated for biochemical disease-free survival included patient age, clinical stage, Gleason score, and pretreatment prostate-specific antigen. Treatment parameters included use of supplemental external-beam radiation therapy and choice of isotope. RESULTSThe 5-year actuarial biochemical disease-free survival rate was 79.9%. In multivariate analysis, preimplantation prostate-specific antigen (P = 0.008) was the only clinical or treatment parameter that predicted for biochemical failure. The mean and median posttreatment prostate-specific antigen levels were 0.13 ± 0.22 ng/mL and < 0.1 ng/mL, respectively. DISCUSSIONAt a median follow-up of 53.7 months, hormone-naive patients with high-risk disease who undergo permanent prostate brachytherapy have a high probability of 5-year biochemical disease-free survival and an apparent plateau on the biochemical disease-free survival curve.
激素- Naïve高危前列腺癌患者接受永久性间质放射治疗和补充外束放射治疗的生化结果
目的:报道未接受激素治疗的高危疾病患者行永久性前列腺近距离放射治疗的5年生化无病预后。还评估了多个临床和治疗参数,以确定是否有任何这些影响生化结果。材料与方法自1995年4月至1999年10月,66例hormone-naïve高危前列腺癌患者接受经会阴超声引导下,采用103Pd或125I进行前列腺周围大范围永久前列腺近距离治疗。高危患者存在以下2个或3个危险因素:Gleason评分≥7,前列腺特异性抗原≥10 ng/mL,临床分期≥T2b (1997 AJCC)。未见病理淋巴结分期。只有一名患者接受了单一治疗,而65名患者在前列腺近距离治疗前接受了补充外束放射治疗。患者年龄中位数为69岁(范围50-81岁)。无患者失访。平均随访时间53.2±14.9个月,中位随访时间53.7个月(范围19.8 ~ 79.7个月)。随访时间自着床当日起计算。生化无病生存是由美国治疗放射学和肿瘤学学会共识定义的。评估生化无病生存的临床参数包括患者年龄、临床分期、Gleason评分和预处理前列腺特异性抗原。治疗参数包括使用辅助外束放射治疗和选择同位素。结果5年精算生化无病生存率为79.9%。在多因素分析中,植入前前列腺特异性抗原(P = 0.008)是预测生化失败的唯一临床或治疗参数。治疗后前列腺特异性抗原水平的平均值和中位数分别为0.13±0.22 ng/mL和< 0.1 ng/mL。在中位53.7个月的随访中,接受永久性前列腺近距离放射治疗的未接受激素治疗的高危疾病患者5年生化无病生存的概率很高,生化无病生存曲线上有明显的平台期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信