跳至主要内容
临床试验/NCT02195141
NCT02195141Unknown2 期

Randomized Phase II Tiral of Using SIB-IMRT in Preoperative Radiotherapy for Locally Advanced Rectum Cancer

Chinese Academy of Medical Sciences2 个研究点 分布在 1 个国家目标入组 104 人开始时间: 2014年1月最近更新:
适应症

试验速览

阶段
2 期
入组人数
104
试验地点
2
主要终点
• Pathological complete remission rate (pCR)

研究概览

简要总结

Pathological complete response, (pCR) correlates with a favorable overall prognosis in locally advanced rectal cancer patients underwent preoperative chemoradiation, so obtaining a pCR might be beneficial. The aim of the study is to investigate safety and efficacy of preoperative SIB-IMRT(56Gy) combine with capecitabine. primary endpoint is pathological complete remission rate.

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 75 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

  • 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

• Pathological complete remission rate (pCR)

时间窗: after pathological examination of surgical speciments (6-8 weeks after chemoradiation)

次要结局

  • Number of participants with adverse events (according to the National Cancer Institute (NCI) - Common Terminology Criteria for Adverse Events v3.0 (CTCAE)(during preoperative treatment and after surgery for 5 years)

研究者

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

Hua Ren

Attending physician

Chinese Academy of Medical Sciences

研究点 (2)

Loading locations...

相似试验