Freeman Debra, Dickerson Gregg, Perman Mark
Naples Radiation Oncology , Naples, FL , USA.
Anova Cancer Center , Denver, CO , USA.
Front Oncol. 2015 Jan 22;4:369. doi: 10.3389/fonc.2014.00369. eCollection 2014.
To report on the design, methodology, and early outcome results of a multi-institutional registry study of prostate cancer radiosurgery.
The Registry for Prostate Cancer Radiosurgery (RPCR) was established in 2010 to further evaluate the efficacy and toxicity of prostate radiosurgery (SBRT) for the treatment of clinically localized prostate cancer. Men with prostate cancer were asked to voluntarily participate in the registry. Demographic, baseline medical, and treatment-related data were collected and stored electronically in a Health Insurance Portability and Accountability Act-compliant database, maintained by Advertek, Inc. Enrolled men were asked to complete short, multiple choice questionnaires regarding their bowel, bladder, and sexual function. Patient-reported outcome forms were collected at baseline and at regular intervals (every 3-6 months) following treatment. Serial prostate-specific antigen measurements were obtained at each visit and included in the collected data.
From July 2010 to July 2013, nearly 2000 men from 45 participating sites were enrolled in the registry. The majority (86%) received radiosurgery as monotherapy. At 2 years follow-up, biochemical disease-free survival was 92%. No Grade 3 late urinary toxicity was reported. One patient developed Grade 3 gastrointestinal toxicity (rectal bleeding). Erectile function was preserved in 80% of men <70 years old. Overall compliance with data entry was 64%.
Stereotactic radiosurgery is an alternative option to conventional radiotherapy for the treatment of organ-confined prostate cancer. The RPCR represents the collective experience of multiple institutions, including community-based cancer centers, with outcome results in keeping with published, prospective trials of prostate SBRT.
报告一项前列腺癌放射外科多机构注册研究的设计、方法及早期结果。
前列腺癌放射外科注册研究(RPCR)于2010年设立,以进一步评估前列腺放射外科(SBRT)治疗临床局限性前列腺癌的疗效和毒性。邀请前列腺癌患者自愿参与该注册研究。收集人口统计学、基线医学及治疗相关数据,并以电子方式存储在由Advertek公司维护的符合《健康保险流通与责任法案》的数据库中。要求入组男性完成关于其肠道、膀胱和性功能的简短多项选择题问卷。在基线及治疗后定期(每3 - 6个月)收集患者报告的结果表格。每次就诊时均进行连续前列腺特异性抗原测量,并纳入收集的数据中。
2010年7月至2013年7月,来自45个参与站点的近2000名男性入组该注册研究。大多数(86%)接受放射外科作为单一疗法。在2年随访时,生化无病生存率为92%。未报告3级晚期泌尿毒性。1例患者发生3级胃肠道毒性(直肠出血)。70岁以下男性中80%的勃起功能得以保留。数据录入的总体依从率为64%。
立体定向放射外科是治疗器官局限性前列腺癌的传统放疗的替代选择。RPCR代表了多个机构(包括社区癌症中心)的集体经验,其结果与已发表的前列腺SBRT前瞻性试验一致。