Evaluation de O-(2-[18F]-Fluoroethyl)-L-Tyrosine, a New Tracer PET, in the Diagnosis of Low Grade Glioma (PET-FETII)
Primary Purpose
Low Grade Glioma
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
O-(2[18F]FLUOROETHYL)-L-TYROSINE
Sponsored by
About this trial
This is an interventional diagnostic trial for Low Grade Glioma focused on measuring : Low grade glioma, PET, FET, MRI, Standardized uptake value
Eligibility Criteria
Inclusion Criteria:
Patients over 18 years
- Diagnosis of glioma grade II referred on clinical and MRI morphologic
- Realization of a brain MRI in preoperative condition of neuronavigation (MRI sequences including axial T2, Flair, T1, T1 with gadolinium) in a within 1 month with FET PET.
- Histological examination scheduled within one month with FET PET by resection (complete or partial) or by biopsy
- Patients who signed informed consent
- No against-indication for PET
- No against-indications to MRI
Exclusion Criteria:
- Grade II glioma who have received specific treatment with radiotherapy and or chemotherapy.
- Pregnant or breastfeeding women.
- Weight greater than 120 Kg
- against-indication to PET
- against- indication gadolinium
- Possible side effects to MRI (magnetic foreign bodies, pacemaker, congestive severe renal).)
- Patient under guardianship
- No coverage by social security
Sites / Locations
- CHU de CAEN
- Hôpital de la Pitié Salpétrière
- UHToulouse
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
FET imaging
Arm Description
FET Imaging. Patient 0.1 mCi / kg (maximum 185 MBq) of FET with 'O-(2[18F]FLUOROETHYL)-L-TYROSINE' will be injected through the venous catheter. At the same time, will trigger a PET 3D dynamic acquisition of 60 minutes (5 pictures 1 minute and 11 images of 5 minutes)
Outcomes
Primary Outcome Measures
Determine the overall discriminating capacity of FET-PET in the diagnosis of glioma grade II (referring to current diagnostic gold standard represented by the histopathological examination of a tumor sample).
Secondary Outcome Measures
- Determine the threshold with the highest positive likelihood ratio. - Determine the threshold with the highest positive likelihood ratio.
Assess the concordance of the data-FET PET and MRI morphological data reported to histological diagnostic
Evaluate the positive and negative predictive value of this threshold in order to improve the delineation of the tumor area
Full Information
NCT ID
NCT02286531
First Posted
November 4, 2014
Last Updated
August 18, 2015
Sponsor
University Hospital, Toulouse
1. Study Identification
Unique Protocol Identification Number
NCT02286531
Brief Title
Evaluation de O-(2-[18F]-Fluoroethyl)-L-Tyrosine, a New Tracer PET, in the Diagnosis of Low Grade Glioma
Acronym
PET-FETII
Official Title
Evaluation de O-(2-[18F]-Fluoroethyl)-L-Tyrosine (or FET), a New Tracer PET (Positron Emission Tomography) , in the Diagnosis of Low Grade Glioma
Study Type
Interventional
2. Study Status
Record Verification Date
August 2015
Overall Recruitment Status
Completed
Study Start Date
June 2010 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Toulouse
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Determine the overall discriminatory ability of FET PET in the diagnosis of glioma grade II (referring to the current diagnostic gold standard represented by the histopathology exam of a tumor sample).
Detailed Description
Low-grade glioma is a malignant tumor of young adults (12.5% of gliomas, incidence of 0.99 / 100,000). Median survival, linked to anaplastic transformation is estimated between 7 and 10 years, with great individual variability in the rate of evolution. The morphological MRI, standard assessment tool at present, suffers from many limitations, especially concerning the positive diagnosis, the targeting of surgical biopsies and tumor delineation which is essential to treatment The study design is a validation study of a new diagnostic procedure. This study is prospective, no randomized, multicenter involving 10 centers (Toulouse University Hospital, Caen, Tours, AP-HP Pitie Salpetriere, Lille, Angers, Rennes, Nîmes, Nantes and Nancy). Will be eligible patients in whom the diagnosis of grade II glioma is suspected according to clinical data and MRI, after evaluation and multidisciplinary meeting at which histological confirmation is scheduled within a maximum period of one month.
FET PET scans will be performed before any procedure or surgical treatment and the data will be merged with MRI. The gold standard is histological examination or biopsy material, or complete resection of the tumor. A minimum of three biopsies per patient will be realized. The pathologist will not see the results of PET-FET 100 patients will be enrolled over a period of 5 years. The area under the curve will be determined on a non-parametric for each increase in the value of PET-FET at near 10th. The sensitivities, specificities, positive predictive values will be estimated with confidence intervals at 95%. Factors to be considered in the analysis, the intrasubject variability related to the fact that several positive and negative results are found for each subject included. The concordance between the data-FET PET and MRI will be sought.
The expected benefits are a better diagnostic ability of PET-FET which results in a specific targeting of biopsies with fewer tests to false negatives and false positives, thus a better diagnostic yield of this invasive procedure. Furthermore, the characteristics of this test applied to all of the tumor may help to better define the limit between healthy and tumor areas and thus reduce the radiation fields to the volumes strictly necessary. These volumes are currently defined on the results of the only morphological MRI and can be further clarified
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Grade Glioma
Keywords
: Low grade glioma, PET, FET, MRI, Standardized uptake value
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
93 (Actual)
8. Arms, Groups, and Interventions
Arm Title
FET imaging
Arm Type
Experimental
Arm Description
FET Imaging. Patient 0.1 mCi / kg (maximum 185 MBq) of FET with 'O-(2[18F]FLUOROETHYL)-L-TYROSINE' will be injected through the venous catheter. At the same time, will trigger a PET 3D dynamic acquisition of 60 minutes (5 pictures 1 minute and 11 images of 5 minutes)
Intervention Type
Drug
Intervention Name(s)
O-(2[18F]FLUOROETHYL)-L-TYROSINE
Other Intervention Name(s)
FET imaging
Intervention Description
Patient 0.1 mCi / kg (maximum 185 MBq) of FET will be injected through the venous catheter. At the same time, will trigger a PET 3D dynamic acquisition of 60 minutes (5 pictures 1 minute and 11 images of 5 minutes)
Primary Outcome Measure Information:
Title
Determine the overall discriminating capacity of FET-PET in the diagnosis of glioma grade II (referring to current diagnostic gold standard represented by the histopathological examination of a tumor sample).
Time Frame
TEP and MRI Imagy 1 month before surgery
Secondary Outcome Measure Information:
Title
- Determine the threshold with the highest positive likelihood ratio. - Determine the threshold with the highest positive likelihood ratio.
Time Frame
1 month before surgery
Title
Assess the concordance of the data-FET PET and MRI morphological data reported to histological diagnostic
Time Frame
1 month before surgery
Title
Evaluate the positive and negative predictive value of this threshold in order to improve the delineation of the tumor area
Time Frame
1 month before surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients over 18 years
Diagnosis of glioma grade II referred on clinical and MRI morphologic
Realization of a brain MRI in preoperative condition of neuronavigation (MRI sequences including axial T2, Flair, T1, T1 with gadolinium) in a within 1 month with FET PET.
Histological examination scheduled within one month with FET PET by resection (complete or partial) or by biopsy
Patients who signed informed consent
No against-indication for PET
No against-indications to MRI
Exclusion Criteria:
Grade II glioma who have received specific treatment with radiotherapy and or chemotherapy.
Pregnant or breastfeeding women.
Weight greater than 120 Kg
against-indication to PET
against- indication gadolinium
Possible side effects to MRI (magnetic foreign bodies, pacemaker, congestive severe renal).)
Patient under guardianship
No coverage by social security
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pierre Payoux, MD PHD
Organizational Affiliation
University Hospital, Toulouse
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU de CAEN
City
Caen
ZIP/Postal Code
14033
Country
France
Facility Name
Hôpital de la Pitié Salpétrière
City
Paris
Country
France
Facility Name
UHToulouse
City
Toulouse
ZIP/Postal Code
31000
Country
France
12. IPD Sharing Statement
Learn more about this trial
Evaluation de O-(2-[18F]-Fluoroethyl)-L-Tyrosine, a New Tracer PET, in the Diagnosis of Low Grade Glioma
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