IRCT201501059979N2已完成2 期
Study of efficacy and safety of low-dose rate endorectal brachytherapy in patients with clinical stage T2N1 or T3-4N0-2 resectable low rectal cancer
Vice chancellor for research,, Shiraz University of Medical Sciences0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 years 至 90 years（—）
- 性别
- All
入选标准
- •Inclusion Criteria:
- •Pathologically proved adenocarcinoma of the rectum
- •Age 18 or older
- •Clinically staged II-III tumor by MRI and/or EUS
- •ECOG performance status of 0 or 1
- •Tumors located at up to10 cm of the anus
- •No previous history of malignancy, pelvic radiotherapy or chemotherapy
- •Normal or adequate bone marrow reserve
- •Normal or adequate liver and kidney function
排除标准
- •Patients with tumors >12 cm from the anal verge.
- •Near obstructing or bulky tumors which will not allow application of the endorectal applicator before or after chemoradiation
- •Patients with distant metastatic disease
- •Prior history of radiation therapy to the pelvis
- •Prior history of chemotherapy for rectal cancer
- •Active connective tissue disease such as scleroderma or Crohn's disease
- •Uncontrolled diabetes mellitus, hypertension or recent cardiovascular disease
- •Significant neuropathy
- •Any previous or recent hypersensitivity or contraindication for chemotherapy agents
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