A Study of a New PET Scanner in People With Cancer
Purpose
The researchers are doing this study to test the capabilities of a new total-body PET scanner called the Biograph Vision Quadra. The researchers want to learn whether this scanner can produce better PET/CT images and provide more useful imaging information than standard PET/CT scanners.
Conditions
- Non Small Cell Lung Carcinoma NSCLC
- Head and Neck Cancer
- Prostate Cancer
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
Eligibility Criteria for objective #1: - Patients with histologically-confirmed non-small cell lung carcinoma (NSCLC) with a single or multiple lung nodules. - Patients who are undergoing a planned PET-CT scan at main campus of MSK. - Patients must be ≥ 18 years old Eligibility Criteria for objective #2: - Patients with disease within the chest, abdomen or pelvis, who could benefit from visualizing the pharmacokinetics of radiotracer uptake within all disease sites simultaneously. - Patients with metastatic prostate or head and neck cancer. - Patients with prostate cancer who are undergoing a 68Ga-PSMA or 18F-FDG scan at the main campus of MSK. - Patients with head and neck cancer who are undergoing a 18F-FDG scan at the main campus of MSK - Patients must be ≥ 18 years old Eligibility Criteria for objective #3: - Patients with histologically-confirmed cancer from all three groups (lung cancer, head and neck cancer, prostate cancer). - Patients who are undergoing an 68Ga-PSMA or 18F-FDG or an [18F]-fluormisonidazole PET-CT scan at the main campus of MSK. - Patients willing to return to the MITS clinc for late imaging session between 2 to 6 hours after the PET radiotracer injection. (In current practice, FDG is imaged between 1 and 1.5 hours post injection, and FMISO is imaged between 2.5 and 3 hours post injection) - Patients must be ≥ 18 years old
Exclusion Criteria
- Patients who suffer from claustrophobia. - Women who are pregnant or breast-feeding. - Patients < 18 years of age
Study Design
- Phase
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
| Patients with lung, head and neck, and prostate cancer | The only investigational aspect of this quality improvement protocol is the acquisition of additional PET/CT imaging data (e.g. breath-hold, dynamic, and/or delayed acquisition) in patients who are already scheduled to receive a PET/CT scan as part of standard of care or under an existing clinical trial. |
|
Recruiting Locations
Basking Ridge, New Jersey 07920
Heiko Schoder, MD
212-639-8001
Middletown, New Jersey 07748
Heiko Schoder, MD
212-639-8001
Montvale, New Jersey 07645
Heiko Schoder, MD
212-639-8001
Commack, New York 11725
Heiko Schoder, MD
212-639-8001
Harrison, New York 10604
Heiko Schoder, MD
212-639-8001
New York, New York 10065
Heiko Schoder, MD
212-639-8001
Rockville Centre, New York 11553
Heiko Schoder, MD
212-639-8001
More Details
- Status
- Recruiting
- Sponsor
- Memorial Sloan Kettering Cancer Center
Detailed Description
This protocol is a quality improvement protocol intended to explore and capitalize on the advanced performance characteristics of a new total body PET scanner; the Biograph Vision Quadra manufactured by Siemens Healthineers.