PSMA-PET Imaging of Salivary Gland Tumours and Other Rare Cancers

Trial Title: PSMA-PET Imaging of Salivary Gland Tumours and Other Rare Cancers

NCT ID: NCT05581979

Condition: Salivary Gland Tumor
Rare Malignant Neoplasm

Conditions: Official terms:
Neoplasms
Salivary Gland Neoplasms
Gallium 68 PSMA-11

Conditions: Keywords:
68-Ga PSMA PET Imaging
Salivary Gland
Radiolabeling
Gallium-68
PET scan
Prostate Specific Membrane Antigen
Adenocystic Carcinoma
Rare Tumours

Study type: Observational

Overall status: Active, not recruiting

Study design:

Time perspective: Prospective

Intervention:

Intervention type: Diagnostic Test
Intervention name: 68-Ga PSMA PET scan
Description: On the scheduled visit date for the study, - An intravenous cannula (plug) will be inserted in a vein in the participant's arm, through which the 68-Ga PSMA radiotracer for the scan will be injected. The infusion will take about 1-2 minutes. - PET imaging will be performed with a dedicated PET/CT scanner. 2.5-6.0 mCi (depending on weight of the patient) of PSMA radiotracer will be injected intravenously.
Arm group label: 68-Ga PSMA PET scan

Summary: The objectives of this pilot feasibility study, which is on the use of 68-Ga PSMA PET imaging of salivary gland tumours, are - to determine the proportion of patients with high PSMA-ligand uptake on Ga-68 PSMA imaging in locally advanced, recurrent or metastatic salivary gland cancers and other rare cancer; and - to determine if in vitro PSMA expression correlates to PSMA-ligand uptake on Ga-68 PSMA imaging in locally advanced, recurrent or metastatic salivary gland cancers and other rare cancers. The hypotheses of this study are that there is high PSMA-ligand uptake on Ga-68 PSMA imaging in locally advanced, recurrent or metastatic salivary gland cancers and other rare cancers; and that in vitro PSMA expression correlates to PSMA-ligand uptake on Ga-68 PSMA imaging.

Detailed description: The potential participant will be screened and confirmed for eligibility by the appropriate study-team member. A signed IRB approved informed consent will be obtained prior to conducting any study-related procedures. On the scheduled visit date for the study, - An intravenous cannula (plug) will be inserted in a vein in the participant's arm, through which the 68-Ga PSMA radiotracer for the scan will be injected. The infusion will take about 1-2 minutes. - PET imaging will be performed with a dedicated PET/CT scanner. 2.5-6.0 mCi (depending on weight of the patient) of PSMA radiotracer will be injected intravenously. - A PET scan will be done around 60 minutes after the injection of the 68-Ga PSMA imaging agent. - During imaging, the participant will be asked to lie still and may be asked to hold his/her breath for a few seconds. - Imaging will be performed using a PET/CT, which will take 30 to 40 minutes to complete. Imaging of the body from vertex to mid thigh or feet will be obtained. - After the completion of the scan, the plug will be removed. A Final Study Visit will take place on that one scheduled day. The participant will not need to visit the doctor's office during the course of the study outside of their usual scheduled doctor's follow up appointments.

Criteria for eligibility:

Study pop:
Patients would have to have histologically confirmed diagnoses, are above 21 years of age, have no contraindication to 68Ga-PSMA PET/CT and able to give consent.

Sampling method: Non-Probability Sample
Criteria:
Inclusion Criteria: - Locally advanced, metastatic or locally recurrent salivary gland cancers OR rare cancers (Examples of rare cancers: thyroid ca, cholangio ca, pancreatic ca, gall bladder ca, sarcoma) - Sample of biopsied tissue available for analysis - Histologically confirmed diagnoses - Above 21 years of age - Able to provide informed consent Exclusion Criteria: - Those who do not meet above inclusion criteria - Diagnosis of haematological malignancies - Patients with more than one cancer diagnosis - Contraindication to 68Ga-PSMA PET/CT - E.g.: pregnant patients, breast feeding patients, renal impairment, liver impairment, allergy to components of the test - Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow up schedule - Ongoing participation in any other clinical trial

Gender: All

Minimum age: 21 Years

Maximum age: 99 Years

Healthy volunteers: No

Locations:

Facility:
Name: National Cancer Centre Singapore

Address:
City: Singapore
Zip: 169610
Country: Singapore

Start date: January 26, 2022

Completion date: June 2024

Lead sponsor:
Agency: National Cancer Centre, Singapore
Agency class: Other

Source: National Cancer Centre, Singapore

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05581979