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临床试验/NCT02635256
NCT02635256已完成不适用

Hypofractionated Radiosurgery for Localised Prostate Cancer

University Hospital Schleswig-Holstein10 个研究点 分布在 1 个国家目标入组 85 人开始时间: 2015年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
85
试验地点
10
主要终点
Late toxicity measured with Radiation Therapy Oncology Group-(RTOG)-Score

研究概览

简要总结

Hypofractionated radiosurgery has been investigated in a few trials and appears to be safe and feasible.

Investigators initiated this multicenter phase II prospective trial to analyse feasibility (toxicity) of hypofractionated radiosurgery with 5 fractions in patients with localised prostate cancer, who are ineligible for the "PREFERE trial" under the hypothesis that the ratio of patients with late toxicity ≥ grade 2 after 1 year amounts 2,8% and is significant lower than 17.5%.

详细描述

Experimental radiosurgery of prostate with 5 fractions each with 7,00 Gy (total application rate of 35,00 Gy).

Planned visits are: Baseline, visits at every radiation day and four follow ups (4-6 weeks, 3 months, 6 months and one year after last day of radiation).

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
60 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Localised, histopathologically confirmed Prostate Cancer (cT1-3 N0 M0)
  • Gleason-grade ≤7
  • Guideline-based staging
  • Age ≥ 60 years
  • PSA < 15 ng/ml
  • Volume of the prostate <80 cm³
  • IPSS-Score ≤12
  • Written informed consent

排除标准

  • History of prior pelvic radiotherapy
  • Contraindication to MRI or Fiducial marker implantation (e.g. allergy to gold),
  • Immunosuppressive therapy
  • Relevant comorbidity thought to adversely affect treatment compliance,
  • Legal incapacity or lack of informed consent

结局指标

主要结局

Late toxicity measured with Radiation Therapy Oncology Group-(RTOG)-Score

时间窗: 12-15 months after radiotherapy

次要结局

  • Acute toxicity analysed by Adverse Event (AE)- and Serious Adverse Event (SAE)-reports.(through study completion)
  • International Prostate Symptom Score (IPSS)(Screening and 3, 6-9 and 12-15 months after radiotherapy)
  • Prostate Specific Antigen (PSA)(At the time of inclusion and 1, 3, 6-9 and 12-15 months after radiotherapy)
  • EORTC Quality of Life Questionnaire (QLQ) C30(At the time of inclusion and 12-15 months after radiotherapy)

研究者

发起方
University Hospital Schleswig-Holstein
申办方类型
Other
责任方
Principal Investigator
主要研究者

Juergen Dunst, Prof.

Prof. Dr. med. Juergen Dunst

University Hospital Schleswig-Holstein

研究点 (10)

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