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Positron Emission Tomography/Computed Tomography Scanning Before Surgery in Patients With Non-Small Cell Lung Cancer, Colorectal Cancer, Breast Cancer, Esophageal Cancer, or Head and Neck Cancer

U

University College London (UCL) Cancer Institute

Status

Unknown

Conditions

Breast Cancer
Esophageal Cancer
Lung Cancer
Head and Neck Cancer
Colorectal Cancer

Treatments

Procedure: therapeutic conventional surgery
Radiation: fludeoxyglucose F 18
Other: laboratory biomarker analysis
Procedure: infrared thermography
Other: 18F-fluoromisonidazole
Radiation: [18F]-ML-10
Other: fluorescence angiography
Radiation: rubidium Rb-82
Procedure: magnetic resonance imaging

Study type

Interventional

Funder types

Other

Identifiers

NCT01254591
UCL-TUMOR-ANGIOGENESIS
CDR0000689973
EU-21086

Details and patient eligibility

About

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.

Full description

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.

Enrollment

500 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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