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

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

ArmDescriptionAssigned 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.
  • Diagnostic Test: Biograph Vision Quadra scanner
    new total-body PET scanner, 1 or 2 additional scans with the Biograph Vision Quadra scanner.
  • Diagnostic Test: PET/CT
    Scheduled PET/CT scan

Recruiting Locations

Memorial Sloan Kettering Basking Ridge (Consent Only)
Basking Ridge, New Jersey 07920
Contact:
Heiko Schoder, MD
212-639-8001

Memorial Sloan Kettering Monmouth (Consent Only)
Middletown, New Jersey 07748
Contact:
Heiko Schoder, MD
212-639-8001

Memorial Sloan Kettering Bergen (Consent Only )
Montvale, New Jersey 07645
Contact:
Heiko Schoder, MD
212-639-8001

Memorial Sloan Kettering Suffolk-Commack (Consent Only)
Commack, New York 11725
Contact:
Heiko Schoder, MD
212-639-8001

Memorial Sloan Kettering Westchester (Consent Only)
Harrison, New York 10604
Contact:
Heiko Schoder, MD
212-639-8001

Memorial Sloan Kettering Cancer Center
New York, New York 10065
Contact:
Heiko Schoder, MD
212-639-8001

Memorial Sloan Kettering Nassau (Consent Only)
Rockville Centre, New York 11553
Contact:
Heiko Schoder, MD
212-639-8001

More Details

Status
Recruiting
Sponsor
Memorial Sloan Kettering Cancer Center

Study Contact

Heiko Schoder, MD
212-639-8001
schoderh@mskcc.org

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.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.