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临床试验/NCT01053923
NCT01053923撤回不适用

A Feasibility Study of MRI in Assessment of Primary Tumor During Chemoradiation for Anal Canal and Perianal Cancer

University Health Network, Toronto0 个研究点开始时间: 2009年12月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
主要终点
Primary tumor dimensions at simulation and during week 3 and last week of fractionated radiotherapy from MRI

研究概览

简要总结

The purpose of this study is to establish a prospective database of anal canal and perianal cancer patients treated with IMRT and chemotherapy with curative intent at PMH for the purposes of investigating MRI-derived primary tumor parameters. Patients who decide to participate in this study will be treated according to standard treatment policies and radiation therapy planning protocols at Princess Margaret Hospital (PMH) with radiation therapy +/- chemotherapy. IMRT for all treatment phases of radiotherapy has been implemented as standard treatment. Surgery is reserved for salvage treatment.

详细描述

Anal cancer is an uncommon cancer, accounting for 2% of gastrointestinal cancers. Prognostic factors include tumor differentiation and staging, along with patient gender, race, and socioeconomic status. The standard of care is radical chemoradiation with 5-fluorouracil and mitomycin C, with surgery reserved for salvage. Intensity modulated radiation therapy (IMRT) is a specialized radiotherapy technique that may be used for anal cancer. IMRT allows the radiation dose to conform to the three-dimensional shape of the target volume more than conventional two-dimensional techniques, and it may reduce treatment toxicities without compromising tumor control. At the Princess Margaret Hospital (PMH) since July 2007, IMRT for all treatment phases of radiotherapy has been implemented as standard treatment for patients with anal canal and perianal cancer.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

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

入选标准

  • histological confirmation of invasive primary squamous cell carcinoma or adenocarcinoma of the anal canal or perianal region
  • treatment with curative intent
  • patients who are not eligible for chemotherapy and receive IMRT alone are eligible for evaluation
  • primary anal or perianal cancer evaluable on cross-sectional imaging (CT or MRI) scan
  • ECOG performance status of 0, 1, or 2
  • age > 18 years
  • able to provide informed consent

排除标准

  • evidence of distant metastasis (M1)
  • prior radiation therapy to the pelvis or contraindication to radiotherapy
  • contraindication to MRI imaging
  • known allergy to intravenous Gadolinium
  • renal insufficiency (serum creatinine greater than 150)
  • serious claustrophobia
  • cardiac pacemaker
  • hip prosthesis
  • major medical or psychiatric illness which, in the investigator's opinion, would prevent completion of imaging study

结局指标

主要结局

Primary tumor dimensions at simulation and during week 3 and last week of fractionated radiotherapy from MRI

时间窗: 12 months

Primary tumor perfusion coefficient at simulation and during week 3 and last week of fractionated radiotherapy from MRI

时间窗: 12 months

Primary tumor apparent diffusion coefficient at simulation and during week 3 and last week of fractionated radiotherapy from MRI

时间窗: 12 months

次要结局

  • Change with time from start of radiotherapy course in primary tumor dimensions from MRI(12 months)
  • Change with time from start of radiotherapy course in primary tumor perfusion coefficient from MRI(12 months)
  • Change with time from start of radiotherapy course in primary tumor apparent diffusion coefficient from MRI(12 months)

研究者

申办方类型
Other
责任方
Sponsor

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