跳至主要内容
临床试验/NCT01254591
NCT01254591Unknown不适用

Tumor Angiogenesis in Non-Small Cell Lung (NSCLC), Colorectal, Breast, Esophageal, Head and Neck Cancer: Radiology-Pathology and Prognostic Correlation

University College London (UCL) Cancer Institute1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2006年11月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
500
试验地点
1
主要终点
Clinical, radiological, and pathological correlation

研究概览

简要总结

RATIONALE: Diagnostic procedures, such as positron emission tomography/computed tomography (PET/CT) scanning before surgery, may help measure the extent of disease.

PURPOSE: This clinical trial is studying PET/CT scanning before surgery in patients with non-small cell lung cancer, colorectal cancer, breast cancer, esophageal cancer, or head and neck cancer.

详细描述

OBJECTIVES:

  • To determine the ability of preoperative fludeoxyglucose F 18 positron emission tomography/computed tomography (PET/CT) scanning in assessing tumor angiogenesis in patients with potentially operable non-small cell lung cancer, colorectal cancer, breast cancer, esophageal cancer, or head and neck cancer.
  • To determine the ability of preoperative fludeoxyglucose F 18 PET/CT scanning in assessing prognosis by means of measuring angiogenesis in these patients.

OUTLINE: All patients undergo fludeoxyglucose F 18 positron emission tomography/computed tomography (PET/CT) scanning for staging, tumor perfusion measurement/angiogenesis, and glucose metabolism. If staging confirms operable disease, then the patient proceeds to surgery as planned. Resected tumor tissue samples are examined for tumor angiogenesis in the various cancer types.

Some patients undergo a half-dose of rubidium Rb-82 or 18F-fluoromisonidazole or [18F]-ML-10 PET scan or fluorescence angiography. Patients with colorectal cancer undergo a CT scan for perfusion of the tumor after the staging PET/CT. Patients with breast cancer undergo infrared thermometry as well as a MRI scan for staging and to predict angiogenesis.

After completion of study therapy, patients are followed up at 1 month and then every 6 months for 5 years.

研究设计

研究类型
Interventional
主要目的
Diagnostic

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •DISEASE CHARACTERISTICS:
  • •Diagnosis of non-small cell lung cancer, colorectal cancer, breast cancer, esophageal cancer, or head and neck cancer
  • •Potentially operable disease
  • •Hormone receptor status not specified
  • •PATIENT CHARACTERISTICS:
  • •Not specified
  • •Menopausal status not specified
  • •PRIOR CONCURRENT THERAPY:
  • •Not specified

排除标准

  • 未提供

结局指标

主要结局

Clinical, radiological, and pathological correlation

Prognosis (6-month, 1-year, 3-year, and 5-year mortality including local/distance recurrence rates)

次要结局

未报告次要终点

研究者

发起方
University College London (UCL) Cancer Institute
申办方类型
Other

研究点 (1)

Loading locations...

相似试验