Positron Emission Tomography (PET) Imaging in Stage III Non-small Cell Lung Cancer (PET START Trial)
Non-Small-Cell Lung Carcinoma
About this trial
This is an interventional diagnostic trial for Non-Small-Cell Lung Carcinoma focused on measuring Positron-Emission Tomography, PET Scan, Non-Small-Cell Lung Carcinoma, Diagnosis, Radiation Oncology, Lung Cancer, Randomized Controlled Trial, Oncology, Radiation Planning
Eligibility Criteria
Inclusion Criteria: Histological or cytological evidence of NSCLC. Must have documented pathology report with histology indicated (e.g. squamous, adenocarcinoma, large cell, NSCLC not otherwise specified). Stage III (mediastinal node positive) NSCLC based on conventional staging (e.g. computed tomography [CT] scan of chest and upper abdomen, CT or magnetic resonance imaging [MRI] of brain, bone scan). Suitable for combined modality (chemotherapy and radiation) therapy or radical radiation therapy or trimodality therapy (chemotherapy, radiation and surgery). Exclusion Criteria: Stage IV NSCLC (by conventional staging). Small cell lung cancer. Poor performance status Eastern Cooperative Oncology Group (ECOG) 3-4. Poor pulmonary function precluding radical radiation therapy (Adequate pulmonary reserve for radical radiation therapy. Pulmonary function tests should have forced expiratory volume in 1 second (FEV1) > 1.0 liter or > 40% predicted, diffusing capacity of the lung for carbon monoxide (DLCO) > 45% and/or predicted contralateral FEV1 > 800 cc based on quantitative ventilation perfusion lung scan). Significant concurrent medical problems (e.g. uncontrolled diabetes, active cardiac problems, significant chronic obstructive pulmonary disease). Insulin dependent diabetic where requirements for PET imaging may be problematic. Unable to lie supine for at least 30 minutes in radiation treatment position for imaging with PET. Failure to provide informed consent. Previous PET scan relating to recent cancer diagnosis prior to entry into study. Pregnant or lactating females. Prior thoracic radiation. Prior malignancy within 3 years from randomization (except nonmelanotic skin cancer or carcinoma in situ of the cervix). Administered more than two cycles of chemotherapy prior to radical radiation therapy or concurrent chemoradiation (as part of induction or sequential chemotherapy prior to randomization) for the current malignancy.
Sites / Locations
- Juravinski Cancer Centre
- London Regional Cancer Centre
- Ottawa Hospital Regional Cancer Centre
- Toronto-Sunnybrook Odette Regional Cancer Centre
- Princess Margaret Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
1
2
PET Imaging
Standard Imaging