Lung Cancer Clinical Trial
Official title:
The Use of Breathing Synchronized PET/CT Imaging In the Detection and Quantification of FDG Uptake in Lung Nodules
The purpose of this study is to see if researchers can improve the detection of lung cancer
by using a new method which will help us to take multiple snapshot images of the lungs while
the patient is breathing. We are also investigating whether with the help of this new method
we can better measure the actual amount of radioactivity that is taken up by the cancer. The
name of this new method is respiratory gated PET/CT. Previous research has shown that PET
scans may be useful in investigating whether cancer has spread to other parts of the lung or
body. Using our standard method, smaller cancers are sometimes difficult to detect in the
lungs because the PET images are taken over several minutes and the patient is breathing
during that time. That means the cancer may appear "blurred" on the images (like a poor
photograph) or may not be identified at all. In this study, in addition to the images that
were ordered by your doctor, we will take additional images of your lungs while you are
following a breathing command ("breath in-hold-breath out"). We will then compare the images
of your cancer during the regular PET study with those taken during the breathing commands.
The hypotheses to be tested in this pilot study are:
1. Respiratory gated image acquisition reduces partial volume effects on PET image that
may render lung lesions undetectable.
2. Breath-hold CT may detect small lung lesions that are beyond the limit of detection in
shallow-breathing CT scans, related to respiratory motion which causes blurring
artifacts around smaller lung lesions.
| Status | Completed |
| Enrollment | 26 |
| Est. completion date | December 2009 |
| Est. primary completion date | December 2009 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Age = 18 years old - Patients must have at least one lung lesion or lung cancer on prior chest Xray or chest CT. - Sign informed consent. Eligible patients should give their consent at the beginning of the clinical PET scan. Following clinical CT and PET scans, breathhold CT should follow. Then, these breath-hold CT images will be reviewed by one of the investigating physicians to determine if the patient qualifies for the study. If there is a small lesion (< 5 mm) gated PET images will be acquired. Exclusion Criteria: - Pregnant women are ineligible. - Patients who are unable to follow breathing instructions either due to language difficulties or hearing impairment This will be determined by one of the consenting individuals when they approach the patient to ask for informed consent. - Patients who are too ill to hold their breath. |
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
| Country | Name | City | State |
|---|---|---|---|
| United States | Memorial Sloan Kettering Cancer Center | New York | New York |
| Lead Sponsor | Collaborator |
|---|---|
| Memorial Sloan Kettering Cancer Center |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Pts w/suspected lung lesions will undergo more breath-hold CT scan & if visible lesion(s), gated-PET will be acquired plus clinical PET/CT. Scans will be used to compare how often additional lung lesions can be identified on breath-hold CT, if lesions | 5 years | No |
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