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临床试验/NCT00619515
NCT00619515终止不适用

Prospective Evaluation of Cyberknife Stereotactic Radiosurgery for Low and Low/Intermediate Risk Prostate Cancer

Case Comprehensive Cancer Center8 个研究点 分布在 1 个国家目标入组 73 人开始时间: 2007年12月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
73
试验地点
8
主要终点
Number of Grade 3-5 Adverse Events as Assessed by NCI CTCAE v3.0

研究概览

简要总结

RATIONALE: Stereotactic radiation therapy may be able to send x-rays directly to the tumor and cause less damage to normal tissue.

PURPOSE: This trial is studying the side effects of stereotactic radiation therapy and to see how well it works in treating patients with prostate cancer.

详细描述

OBJECTIVES:

Primary

  • To estimate in both low- and low-to-intermediate-risk groups of patients with prostate cancer, the rate of acute toxicities observed during the 5 years following CyberKnife® stereotactic radiosurgery (SRS).

Secondary

  • To estimate the rate of late grade 3-5 toxicities after SRS in these patients.
  • To measure biochemical disease-free survival of patients treated with this therapy.
  • To measure rates of local failure, distant failure, disease-free survival, disease-specific survival, and overall survival of patients treated with this therapy.
  • To measure quality of life in generic and organ-specific domains in patients treated with this therapy.
  • To evaluate imaging modalities and their potential role in the detection of prostate cancer persistence, recurrence, and/or progression in patients treated with this therapy.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
— 至 120 Years(Child, Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

CyberKnife® stereotactic radiosurgery

Experimental

干预措施: questionnaire administration (Other)

CyberKnife® stereotactic radiosurgery

Experimental

干预措施: implanted fiducial-based imaging (Procedure)

CyberKnife® stereotactic radiosurgery

Experimental

干预措施: stereotactic radiosurgery (Radiation)

结局指标

主要结局

Number of Grade 3-5 Adverse Events as Assessed by NCI CTCAE v3.0

时间窗: Within 90 days of completing treatment

This study's primary goal is to determine the rate of acute grade 3-5 toxicities following CyberKnife treatment. Per RTOG/ECOG, acute toxicity will be defined as occurring within 90 days of completing treatment.

次要结局

  • Disease-specific Survival(Assessed yearly for 5 years)
  • Overall Survival(Assessed yearly for 5 years)
  • Number of Late Grade 3-5 Toxicities as Assessed by NCI CTCAE v3.0(Within 5 years of completing treatment)
  • Biochemical Disease-free Survival(Assessed at months 3,6,12,18,24 and every 6 months through 5 years)
  • Disease-free Survival (Phoenix and ASTRO Definitions)(Assessed yearly for 5 years)
  • Rate of Local Failure(Assessed at months 3,6,12,18,24 and every 12 months through 5 years)
  • Quality of Life as Measured by the Short Form-12 Health Survey, Expanded Prostate Cancer Index Composite, and the American Urological Association Symptom Index, and the Utilization of Sexual Medications/Devices(Survey at 1,6,12 months and yearly up to 5 years)
  • Rate of Distant Failure(Assessed at months 3,6,12,18,24 and every 12 months through 5 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (8)

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