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临床试验/NCT01224392
NCT01224392已完成3 期

Randomized Trial of Preoperative Radiotherapy With an Integrated Simultaneous Boost Compared to Chemoradiotherapy for T3-4 Rectal Cancer

Universitair Ziekenhuis Brussel4 个研究点 分布在 1 个国家目标入组 156 人开始时间: 2010年1月最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
156
试验地点
4
主要终点
reduction in metabolic tumor activity

研究概览

简要总结

The investigators propose a randomized non-inferiority trial that compares preoperative Fluoro Uracil (FU)-based chemoradiotherapy to radiotherapy with a simultaneous integrated boost. In patients with T3-4 rectal cancer, the latter approach is considered preferential with regard to toxicity and cost. The metabolic response of the tumor, as assessed by 18F-2-Fluoro-2-Deoxyglucose-Positron Emission tomography (18F-FDG PET) or PET-CT, will be used as a surrogate marker of cause specific outcome

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 95 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • histopathologically confirmed rectal adenocarcinoma with an inferior border within 15 cm of the anal verge
  • the tumor has to have evidence of T3 or T4 disease on Magnetic Resonance Imaging (MRI) or endoluminal ultrasound

排除标准

  • unresectable metastatic disease
  • Eastern Cooperative Oncology Group (ECOG) performance status > 3
  • patients not deemed fit for radiotherapy, capecitabine or surgery
  • pregnant or lactating patients
  • women with child bearing potential who lack effective contraception
  • patients below 18 years old

结局指标

主要结局

reduction in metabolic tumor activity

时间窗: at baseline and at 5 to 6 weeks after neo-adjuvant therapy

次要结局

  • survival(every 6 months in the first year after completion of radiotherapy and then yearly until 3 years)
  • acute and late toxicity, according to the National Cancer Institute (NCI) - Common Terminology Criteria for Adverse Events v3.0 (CTCAE)(at baseline, every 6 months after completion of radiotherapy and then yearly until 3 years)
  • histological downgrading (Dworak classification)(after the rectum surgery)
  • progression free survival(every 6 months in the first year after completion of radiotherapy and then yearly until 3 years)
  • number of R0, R1 and R2 resections(after the rectum surgery)
  • local control(every 6 months in the first year after completion of radiotherapy and then yearly until 3 years)
  • cost evaluation(during the treatment and follow-ups)
  • quality of life(at baseline, every 6 months in the first year after completion of radiotherapy and then yearly until 3 years)

研究者

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

Mark De Ridder

Head of Radiotherapy Department

Universitair Ziekenhuis Brussel

研究点 (4)

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