Evaluation of a Pneumotachograph (SPI) for the Production of PET and CT Acquisitions Synchronized With Breath for the Assessment of Extension of Lung Cancer (SPI COHERENCE)
Non Small Cell Lung Cancer, Lung Nodule
About this trial
This is an interventional diagnostic trial for Non Small Cell Lung Cancer focused on measuring Lung Cancer, PET/CT, FDG, Respiratory synchronization
Eligibility Criteria
Inclusion Criteria:
Patient for whom there is an indication of PET/CT 18FDG imaging for thoracic oncology ; this indication is consistent with the Standard Options Recommendations or was validated during Multidisciplinary Consultation Meeting :
- Either an extension assessment of non-small cell lung cancer;
- Either the characterization of single pulmonary nodule; Or - the definition of the target volume in radiotherapy.
Patient who meets the following criteria to be eligible for an PET/CT imaging:
- Patient able to maintain a supine position for 60 minutes
- Patient with no bronchopulmonary infection and with no upper aero digestive tract acute infection in progress (increased risk of false positives)
- Age ≥ 18 years
- WHO ≤ 1
- Well-informed written consent signed by the patient and collected before any specific procedure in the study
- Patient member in a national insurance scheme
Exclusion Criteria:
- Patient with a bronchial carcinoid or bronchoalveolar cancer
- Patient with acute bronchopneumopathy
- Not stabilized diabetic patient
- Patient with an absolute indication against spirometry: ongoing pneumothorax or within the previous month, pleural biopsy or puncture within the previous month, hemoptysis, severe asthma, tuberculosis
- Any usual relative indication against spirometry: ongoing bronchial infections, acute asthma, decompensation of chronic respiratory failure, respiratory pain
- Any usual formal indication against imaging examination PET/CT (important claustrophobia)
- Patient unable to follow study procedures
- Pregnant women or nursing mothers can not participate in the study
- Men and women of childbearing age must use effective contraception at study entry and throughout the study
- Any other medical conditions making the inclusion of the patient in the study inappropriate in the opinion of the investigator
- Patient under legal guardianship
Sites / Locations
- Institut Claudius REGAUD
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
SPI Medical device
reference medical device : RPM
SPI medical device used during PET/CT 4D imaging in a synchronized mode centered on the thorax.
Reference medical device (RPM) used simultaneously during PET/CT 4D imaging in a synchronized mode centered on the thorax.