跳至主要内容
临床试验/NCT01148056
NCT01148056终止不适用

A Phase II Study of Neoadjuvant Short Course Intensity Modulated Radiation Therapy (IMRT) for Patients With Rectal Cancer: An Analysis of Quality of Life and Biomarkers of Response

Massachusetts General Hospital1 个研究点 分布在 1 个国家目标入组 2 人开始时间: 2010年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
2
试验地点
1
主要终点
Bowel Quality of Life

研究概览

简要总结

This study will investigate short course radiation therapy using IMRT as an alternative to standard chemo radiation because prior studies have shown that this method of treatment will potentially reduce some fo the side effects of standard treatment, improve quality of life, and help to control the growth of rectal cancer cells. IMRT is a type of radiation that uses computer-generated images to match radiation to the size and shape of the tumor. Since the intensity of each radiation beam can be controlled, the radiation dose can wrap around normal tissue which allows the study doctor to deliver a higher dose of radiation to the tumor with less damage to nearby healthy tissue. The purpose of this research study is to see what impact this treatment will have on quality of life, as well as to see if there are any late side effects that come about after the participant has completed the treatment.

详细描述

  • Radiation treatment to the rectum will be given once a day, for 5 days. Each radiation treatment will take about 20-30 minutes.
  • The following procedures will be performed on day 1 of radiation treatment: physical examination, blood tests and quality of life questionnaire.
  • During radiation treatment a physical examination will be performed once during the 5 days of radiation treatment. A Quality of Life Questionnaire will be administered on the last day of radiation treatment.
  • Surgery will be performed within 3-14 days after the last day of radiation treatment.

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

入选标准

  • •Histologically or cytologically confirmed adenocarcinoma of the rectum
  • •T3 or N+ disease by MRI or endoscopic ultrasound. Metastatic disease is permitted, except for known brain metastases, as long as local treatment with RT and surgery is recommended.
  • •Prior chemotherapy is permitted. For patients who have previously received bevacizumab, the last dose must be greater than 4 weeks prior to initiation of radiation therapy.
  • •18 years of age or older
  • •Life expectancy of greater than 3 months
  • •ECOG (Eastern Cooperative Oncology Group) Performance Status of 0, 1 or 2
  • •Normal organ and marrow function as outlined in the protocol
  • •Women of child-bearing potential and men must agree to use of adequate contraception prior to study entry and for the duration of study participation

排除标准

  • •Pelvic radiotherapy prior to entering the study or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier
  • •Participants may not be receiving any other investigational agents. Patients may not be receiving any other treatment for their rectal cancer during study participation
  • •Participants with known brain metastases are excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events
  • •History of known radiation sensitivity syndrome
  • •History of inflammatory bowel disease
  • •Active scleroderma or CREST syndrome
  • •Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
  • •Pregnant or nursing women

研究组 & 干预措施

Short course IMRT

Experimental

Patients will receive short course IMRT (Intensity Modulated Radiation Therapy) prior to surgery. Dose will be 5 Gy x 5, followed by surgery the week after

干预措施: Intensity Modulated Radiation Therapy (Radiation)

结局指标

主要结局

Bowel Quality of Life

时间窗: 2 years

To determine the rate of fecal incontinence at 1 year in patients undergoing an low anterior resection (LAR), as measured by bowel quality of life measure after preoperative conformal radiation therapy delivered in one week for rectal cancer.

次要结局

  • Pelvic Control Rate(2 years)
  • Quantity of Circulating Tumor Cells(2 years)
  • Surgical Complication Rate(2 years)
  • Tissue Microarray(2 years)
  • Accuracy(2 years)

研究者

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

Theodore Sunki Hong

Radiation Oncologist

Massachusetts General Hospital

研究点 (1)

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