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A Comparison of NETSPOT Imaging Versus F-FDG-PET in Head and Neck Cancer Patients

Primary Purpose

Head and Neck Squamous Cell Carcinoma

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
The isotope 68Ga, NETSPOT and 18F-FDG-PET/CT
Sponsored by
West Virginia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Head and Neck Squamous Cell Carcinoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Patients with suspected or diagnosed HNSCC undergoing planned 18F FDG PET/CT at the time of primary diagnosis or after completion of treatment.

Exclusion Criteria:

Inability to undergo 18F-FDG-PET/CT imaging due to medical comorbidities

Sites / Locations

  • West Virginia University MedicineRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Proof of Concept

Arm Description

The isotope 68Ga, available as NETSPOT and 18F-FDG-PET/CT per established protocol will both be administered

Outcomes

Primary Outcome Measures

Detection and Staging of Head and Neck Squamous Cell Carcinoma
NETSPOT imaging will be at least equivalent to 18F FDG PET/CT in the detection and staging of HNSCC. This will be done using Standard Uptake Value (SUV) measurements.

Secondary Outcome Measures

Detection of primary site for Head and Neck Squamous Cell Carcinoma
The Combination of NETSPOT imaging and 19F FDG PET/CT will have increased specificity for detecting the primary site for HNSCC of unknown primary than 18F FDG PET/CT alone. This will be done using Standard Uptake Value (SUV) measurements.
Detection of disease recurrence and metastasis following treatment
The combination of NETSPOT imaging and 18F FDG PET/CT, will have increased specificity for detecting disease recurrence and metastasis following treatment than 18F FDG PET/CT alone. This will be done using Standard Uptake Value (SUV) measurements.

Full Information

First Posted
June 22, 2018
Last Updated
April 23, 2019
Sponsor
West Virginia University
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1. Study Identification

Unique Protocol Identification Number
NCT03602911
Brief Title
A Comparison of NETSPOT Imaging Versus F-FDG-PET in Head and Neck Cancer Patients
Official Title
A Comparison of NETSPOT Imaging Versus F-FDG-PET in Head and Neck Cancer Patients
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2019 (Actual)
Primary Completion Date
July 30, 2019 (Anticipated)
Study Completion Date
July 31, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
West Virginia University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a proof-of-concept trial to compare 18F-FDG-PET/CT with NETSPOT (68Ga-DOTA-TATE), a commercially available radiotracer packet that utilizes 68Ga to image SSTR-specific tissue.
Detailed Description
Patients meeting inclusion criteria will be consented at the time of scheduling. All patients will undergo 18F-FDG-PET/CT per established protocol. Following 18F-FDG-PET/CT, the patient will undergo NETSPOT imaging with the AAA-provided dose. These scans will be performed no less than 8 hours, no more than 7 days apart. For patients undergoing same-day imaging, NETSPOT imaging will be performed prior to 18F-FDG-PET/CT. Following imaging, both 18F-FDG-PET/CT and NETSPOT imaging will be compared by trained neuroradiologists for SUV values and concordance with known sites of disease. Biopsies will be performed as is standard to verify all sites of primary or metastatic disease. Patients with oropharyngeal tumors will have HPV testing performed via the standard of care surrogate marker p16. Patients with p16-positive tumors will be recorded and analyzed separately for the above measures. Patients will be followed for a total of 1 year after the study and outcomes of overall survival, disease-free survival, presence and site of recurrence and development of metastatic disease will be recorded. All gathered data will be compared between reported 18F-FDG-PET/CT and NETSPOT imaging for true positive, true negative, positive predictive value and negative predictive value of patient groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Head and Neck Squamous Cell Carcinoma

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Model Description
Proof of Concept
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Proof of Concept
Arm Type
Other
Arm Description
The isotope 68Ga, available as NETSPOT and 18F-FDG-PET/CT per established protocol will both be administered
Intervention Type
Drug
Intervention Name(s)
The isotope 68Ga, NETSPOT and 18F-FDG-PET/CT
Intervention Description
All patients will undergo 18F-FDG-PET/CT per established protocol. Following 18F-FDG-PET/CT, the patient will undergo NETSPOT imaging
Primary Outcome Measure Information:
Title
Detection and Staging of Head and Neck Squamous Cell Carcinoma
Description
NETSPOT imaging will be at least equivalent to 18F FDG PET/CT in the detection and staging of HNSCC. This will be done using Standard Uptake Value (SUV) measurements.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Detection of primary site for Head and Neck Squamous Cell Carcinoma
Description
The Combination of NETSPOT imaging and 19F FDG PET/CT will have increased specificity for detecting the primary site for HNSCC of unknown primary than 18F FDG PET/CT alone. This will be done using Standard Uptake Value (SUV) measurements.
Time Frame
6 months
Title
Detection of disease recurrence and metastasis following treatment
Description
The combination of NETSPOT imaging and 18F FDG PET/CT, will have increased specificity for detecting disease recurrence and metastasis following treatment than 18F FDG PET/CT alone. This will be done using Standard Uptake Value (SUV) measurements.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with suspected or diagnosed HNSCC undergoing planned 18F FDG PET/CT at the time of primary diagnosis or after completion of treatment. Exclusion Criteria: Inability to undergo 18F-FDG-PET/CT imaging due to medical comorbidities
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Aimie Jones, CCRC
Phone
304- 598-6135
Email
jonesai@wvumedicine.org
First Name & Middle Initial & Last Name or Official Title & Degree
Rusha Patel, MD
Email
rusha.patel@hsc.wvu.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rusha Patel, MD
Organizational Affiliation
West Virginia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
West Virginia University Medicine
City
Morgantown
State/Province
West Virginia
ZIP/Postal Code
26501
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aimie Jones, CCRC
First Name & Middle Initial & Last Name & Degree
Rusha Patel, MD

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

A Comparison of NETSPOT Imaging Versus F-FDG-PET in Head and Neck Cancer Patients

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