Lung Neoplasms Clinical Trial
Official title:
Randomized Study Comparing Standard Staging of Lung Cancer With Extended Staging Including EBUS-TBNA and PET-MRI
The overall aim of this study is to compare standard staging of lung cancer (which includes clinical examination, CT, MRI, bone scan and PET-CT) with comprehensive staging - which includes the new staging methods (PET-MRI and systematic mapping of mediastinal and hilar lymph nodes using endobronchial ultrasound) with respect to disease stage and outcomes of therapy.
The trial is a randomized, explorative study. Patients undergoing examinations for suspicions
of lung cancer (Stage I-III) are randomized to either standard diagnostic work-up for lung
cancer (Arm A, n=75) or comprehensive diagnostic work-up (Arm B, n=75) with standard
examinations plus endobronchial-screening for metastatic lymph nodes (EBUS-TBNA) and PET-MRI.
All patients will undergo todays' standard examination for diagnosing and staging lung
cancer. This will be individualized for each patient according to current guidelines. In
addition to the standard diagnostic work-up, patients in the interventional group (ArmB) will
undergo
1) PET-MRI 2) systematic mediastinal and hilar lymph node mapping using EBUS-TBNA
(endobronchial ultrasound transbronchial needle aspiration of lymph nodes)
1. PET-MRI PET-MRI will be done immediate after the standard PET-CT using the same infusion
of tracer (18-fluorodeoxyglucose, FDG). The sequence protocols used for MRI will be
standardized for the study, according to each body compartment. Measurement of Standard
Uptake Values (SUV) of the tracer (FDG) will be recorded in pathological lesions. In the
mediastinum, each lymph node station will be evaluated with description of visible
nodes.
2. Systematic mediastinal mapping The EBUS-TBNA will be done at the initial bronchoscopy
and using standard conscious sedation according to the local guidelines at St.Olavs
Hospital. Each lymph node station (station 2, 4, 7, 10 and 11 bilateral) will be
examined and all lymph nodes ≥ 0,5 cm in short diameter that is easily accessible will
be punctured for rapid on-site cytological evaluation (ROSE).
After the initial diagnostic work-up is completed, the patient will be given treatment
according to existing guidelines for lung cancer based on the given clinical stage.
For patients undergoing surgery all accessible lymph nodes will be resected according to
standard practice. Every resected lymph node will be carefully named according to the
standard lymph station for comparison with clinical findings.
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