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临床试验/NCT00232453
NCT00232453已完成2 期

A Phase II Protocol of Preoperative Combined Radiation and Chemotherapy for Resectable Primary Rectal Cancer

University Health Network, Toronto2 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2001年3月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
34
试验地点
2
主要终点
Assess acute toxicity and complete remission rate of combined preoperative radiation and chemotherapy

研究概览

简要总结

There is no established standard preoperative treatment in rectal cancer. Two large randomized studies in North America closed from lack of accrual; therefore the only method of assessing preoperative treatment in rectal cancer is from Phase II studies. This study builds on the experience at PMH gained in two previous studies which demonstrated a lower than expected toxicity with concurrent 5FU infusion and external radiotherapy. The current standard at PMH is preoperative radiation, 46Gy in 23 fractions with concurrent 5FU infusion 225mg/m2. An increase of radiation dose and consequent increase in chemotherapy may improve the response rate, but may also increase toxicity. It is proposed to increase the dose of radiotherapy to 50Gy in 25 fractions with concurrent chemotherapy and measure acute toxicity and complete remission rate.

研究设计

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

入排标准

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

入选标准

  • Biopsy proven adenocarcinoma of the rectum
  • Performance status <2 (ECOG, appendix II)
  • Clinical Stage T2 N1-2, T3-4 NO-2, without evidence of distant metastasis

排除标准

  • Prior pelvic irradiation
  • Inflammatory bowel disease
  • Evidence of distant metastasis
  • Performance status >2

结局指标

主要结局

Assess acute toxicity and complete remission rate of combined preoperative radiation and chemotherapy

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (2)

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