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临床试验/NCT02229734
NCT02229734已完成2 期

Fairly Brief Androgen Suppression and Stereotactic Radiotherapy for High Risk Prostate Cancer - Protocol 2

Lawson Health Research Institute1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2014年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
60
试验地点
1
主要终点
Genitourinary and Gastrointestinal Toxicity at 1 year

研究概览

简要总结

This study will explore the combination of a stereotactic body radiation therapy (SBRT) approach combined with one year of luteinizing hormone releasing hormone (LHRH) agonist for older men with high risk prostate cancer, or men unwilling to undertake conventionally fractionated therapy and three years of adjuvant hormone therapy.

The purpose of this study is to examine the safety of a shorter course of radiation treatment combined wtih androgen deprivation therapy.

详细描述

Randomized controlled trials have established the improved efficacy (better biochemical control and disease free survival) of combined radical radiation (70-80 Gy over 7-8 weeks) combined with long term hormone therapy (2-3 years of adjuvant LHRH agonist) compared to a primary hormone therapy or radiation therapy alone in men with locally advanced/high risk disease. While this approach may be tolerable in fit individuals, this combination may not be well tolerated by frail individuals, or those who live at a distance who may find it difficult to attend for 7 weeks of radiation treatments. Those individuals with co-morbidities such as diabetes, coronary artery disease or osteoporosis may have those conditions exacerbated by long term hormone therapy.

The combination of short course radiation and hormone therapy was explored in the FASTR trial. As part of the trial, patients received 12 months of hormone therapy with radiation treatment to the pelvic lymph nodes (dose of 25 Gy in 5 fractions, 1 fraction per week) concomitant with radiation treatment to the prostate (dose of 40 Gy in 5 fractions, 1 fraction per week). The study was discontinued due to toxicity. For the FASTR-2 study, these concerns are being addressed through the use of a lower total dose to the prostate (35 Gy in 5 fractions, 1 fraction per week). Given the uncertainty of the benefit of pelvic nodal radiation in prostate cancer, it was decided to omit the pelvic nodal radiation in the FASTR-2 study. In addition, given the recent evidence supporting the equivalence of 18 months of hormone therapy, compared to 36 months, it was decided to lengthen the duration of hormone therapy in the FASTR-2 study to 18 months (versus 12 months in the FASTR study).

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

入选标准

  • High risk prostate cancer
  • Has had multidisciplinary consultation with radiation oncologist and urologist
  • Age >70 or refuses standard treatment
  • No evidence of extra-prostatic disease on screening bone scan and CT scan (non-contrast CT used for CT simulation acceptable)
  • Signed written and voluntary informed consent provided.
  • Patients must be willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures

排除标准

  • Patients not meeting the eligibility criteria
  • Prior pelvic radiotherapy or brachytherapy
  • Use of anti-coagulation (low molecular weight heparin or Coumadin)
  • History of inflammatory bowel disease, Crohn's disease, diverticulitis or collagen vascular disease (other than rheumatoid arthritis)
  • Previous treatment for malignancy (other than basal or squamous cell skin cancer) within 3 years of prostate cancer diagnosis
  • patients on androgen deprivation therapy > 2 months prior to study enrolment

研究组 & 干预措施

Radiation plus Androgen Supression

Experimental

Radiation plus Androgen Suppression give as stereotactic radiation 7gray (Gy) per week x 5 weeks and leuprolide 45mg every 6 months for 18 months

干预措施: Radiation (Radiation)

Radiation plus Androgen Supression

Experimental

Radiation plus Androgen Suppression give as stereotactic radiation 7gray (Gy) per week x 5 weeks and leuprolide 45mg every 6 months for 18 months

干预措施: Androgen Suppression (Drug)

结局指标

主要结局

Genitourinary and Gastrointestinal Toxicity at 1 year

时间窗: Year 1 of follow-up

Genitourinary and gastrointestinal toxicity measured at year 1 of follow-up using the Common Toxicity Criteria

次要结局

  • Disease Free Survival at 3 years(1, 2, and 3 years of follow-up)
  • Quality of Life(1, 2, and 3 years of follow-up)
  • Genitourinary and Gastrointestinal Toxicity at 2 years(Year 2 of follow-up)
  • Genitourinary and gastrointestinal toxicity measured at 3 years(Year 3 of follow-up)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Glenn Bauman

Principal Investigator

Lawson Health Research Institute

研究点 (1)

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