PSMA-PET Imaging for Advanced ACC/SDC
Primary Purpose
Salivary Gland Cancer, Adenoid Cystic Carcinoma, Salivary Duct Carcinoma
Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
PSMA-PET/CT scan
Sponsored by
About this trial
This is an interventional diagnostic trial for Salivary Gland Cancer focused on measuring 68Ga-PSMA, Positron-Emission Tomography, Immunohistochemistry
Eligibility Criteria
Inclusion Criteria:
- locally advanced, recurrent or metastatic ACC/SDC
- Age ≥ 18 years old
- Ability to provide written informed consent
Exclusion Criteria:
- Contra-indication for PET imaging
- Pregnancy
- Breast feeding
- Severe claustrophobia
- Impaired renal function: MDRD <30 ml/min/1,73 m2
- Impaired liver function: AST and ALT ≥ 2.5 x ULN (≥5 x ULN for patients with liver metastases)
Sites / Locations
- Radboudumc
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
PSMA-PET/CT scan
Arm Description
PSMA-PET/CT imaging in advanced ACC/SDC
Outcomes
Primary Outcome Measures
uptake of 68Ga-PSMA in ACC and SDC
To evaluate the uptake of 68Ga-PSMA in locally advanced, recurrent and metastatic ACC/SDC by performing 68Ga-PSMA-PET/CT scans
Secondary Outcome Measures
SUV of 68Ga-PSMA in ACC/SDC tumors
SUV of 68Ga-PSMA in ACC/SDC tumors
SUV of 68Ga-PSMA in the background
in order to calculate the SUV tumor to background ratio
correlation of SUV and IHC PSMA-staining
Correlate the tumor uptake (SUV) to the degree of immunohistochemical PSMA expression of the primary tumor on archival tissue
new metastases
To establish whether new metastatic lesions are found by 68GA-PSMA-PET/CT imaging
Full Information
NCT ID
NCT03319641
First Posted
September 29, 2017
Last Updated
May 28, 2018
Sponsor
Radboud University Medical Center
Collaborators
Adenoid Cystic Carcinoma Research Foundation
1. Study Identification
Unique Protocol Identification Number
NCT03319641
Brief Title
PSMA-PET Imaging for Advanced ACC/SDC
Official Title
68Ga-PSMA-PET/CT Imaging for Locally Advanced, Recurrent and Metastatic Adenoid Cystic Carcinoma or Salivary Duct Carcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
October 25, 2017 (Actual)
Primary Completion Date
May 14, 2018 (Actual)
Study Completion Date
May 14, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Radboud University Medical Center
Collaborators
Adenoid Cystic Carcinoma Research Foundation
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Diagnostic study which evaluates the level of PSMA expression in patients with locally advanced, recurrent and/or metastatic ACC/SDC of ≥18 years old with 68Ga-PSMA-PET/CT imaging in order to establish whether these patients are eligible for 177Lu-PSMA therapy
Detailed Description
Rationale: PSMA is a transmembrane protein, which is expressed on prostate cancers cells, ACC and other malignancies. In prostate cancer, distant metastases can be visualized sensitively and non-invasively with 68Ga-PSMA-PET/CT scans and if the uptake of 68Ga is high enough, patients can be treated with the β-emitting radionuclide 177Lu-PSMA. In the current study, we will evaluate the uptake of 68Ga-PSMA by performing 68Ga-PSMA-PET/CT scans in advanced ACC and SDC patients. If the uptake is high enough, this will form the rationale for a therapeutic study with 177Lu-PSMA in ACC and SDC.
Objective: The primary objective is to evaluate the uptake of 68Ga-PSMA in locally advanced, recurrent and metastatic ACC/SDC by performing 68Ga-PSMA-PET/CT scans. The secondary objectives are to calculate the SUV tumor-to-background ratio and tumor-to-'healthy salivary gland tissue' ratio. To correlate the SUV to the degree of immunohistochemical PSMA expression of the primary tumor on archival tissue, and to establish whether new metastatic lesions are found by 68GA-PSMA-PET/CT imaging.
Study design: Diagnostic study which evaluates the level of PSMA expression in ACC/SDC patients with 68Ga-PSMA-PET/CT imaging in order to establish whether these patients are eligible for 177Lu-PSMA therapy.
Study population: Patients with locally advanced, recurrent or metastatic ACC/SDC of ≥18 years old.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Salivary Gland Cancer, Adenoid Cystic Carcinoma, Salivary Duct Carcinoma
Keywords
68Ga-PSMA, Positron-Emission Tomography, Immunohistochemistry
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
diagnostic study
Masking
None (Open Label)
Allocation
N/A
Enrollment
25 (Actual)
8. Arms, Groups, and Interventions
Arm Title
PSMA-PET/CT scan
Arm Type
Experimental
Arm Description
PSMA-PET/CT imaging in advanced ACC/SDC
Intervention Type
Diagnostic Test
Intervention Name(s)
PSMA-PET/CT scan
Intervention Description
perform a PSMA-PET/CT scan in patients with locally advanced, recurrent and/or metastastic ACC or SDC
Primary Outcome Measure Information:
Title
uptake of 68Ga-PSMA in ACC and SDC
Description
To evaluate the uptake of 68Ga-PSMA in locally advanced, recurrent and metastatic ACC/SDC by performing 68Ga-PSMA-PET/CT scans
Time Frame
0 days
Secondary Outcome Measure Information:
Title
SUV of 68Ga-PSMA in ACC/SDC tumors
Description
SUV of 68Ga-PSMA in ACC/SDC tumors
Time Frame
0 days
Title
SUV of 68Ga-PSMA in the background
Description
in order to calculate the SUV tumor to background ratio
Time Frame
0 days
Title
correlation of SUV and IHC PSMA-staining
Description
Correlate the tumor uptake (SUV) to the degree of immunohistochemical PSMA expression of the primary tumor on archival tissue
Time Frame
0 days
Title
new metastases
Description
To establish whether new metastatic lesions are found by 68GA-PSMA-PET/CT imaging
Time Frame
0 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
locally advanced, recurrent or metastatic ACC/SDC
Age ≥ 18 years old
Ability to provide written informed consent
Exclusion Criteria:
Contra-indication for PET imaging
Pregnancy
Breast feeding
Severe claustrophobia
Impaired renal function: MDRD <30 ml/min/1,73 m2
Impaired liver function: AST and ALT ≥ 2.5 x ULN (≥5 x ULN for patients with liver metastases)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carla ML van Herpen, MD, PhD
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Radboudumc
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6500HB
Country
Netherlands
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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PSMA-PET Imaging for Advanced ACC/SDC
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