Dosimetry and Biodistribution of [18F]-Fludarabine in Lymphoid Malignancies (FLUDATEP)
Primary Purpose
Untreated B-Chronic Lymphocytic Leukemia or Diffuse Large B Cells Lymphoma Patients
Status
Completed
Phase
Phase 1
Locations
France
Study Type
Interventional
Intervention
[18F] - Fludarabine PET/CT
Sponsored by
About this trial
This is an interventional diagnostic trial for Untreated B-Chronic Lymphocytic Leukemia or Diffuse Large B Cells Lymphoma Patients focused on measuring PET, Chronic lymphocytic Leukemia (CLL), Diffuse Large B Cells Lymphoma (DLBCL), Fludarabine
Eligibility Criteria
Inclusion Criteria:
- Adult over 18
- Signed written informed consent
- Untreated stage B or C chronic lymphocytic leukemia
- Untreated diffuse large B-cell lymphoma
- Eligible for PET-CT
- The subject must be covered by a social security system
Exclusion Criteria:
- Age under 18
- Patients concurrently included in an investigational trial
- Weight over 120 kg
- pregnant women
- active infectious disease
- immune hemolytic anemia
- patients with creatinine clearance < 30 ml/mn
- corticosteroid therapy
Sites / Locations
- University Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
FLUDATEP
Arm Description
[18F] - Fludarabine PET/CT
Outcomes
Primary Outcome Measures
Standardized measure of [18F]-Fludarabine uptake in tumor tissue.
Measure of the Standard Uptake Value (SUV) for each lesion.
Secondary Outcome Measures
Calculation of the equivalent dose to all organs and evaluation of effective dose to the whole body
Full Information
NCT ID
NCT02128945
First Posted
April 9, 2014
Last Updated
September 12, 2016
Sponsor
University Hospital, Caen
Collaborators
CNRS, UMR ISTCT 6301, LDM-TEP Groupe, GIP Cyceron, Caen, France
1. Study Identification
Unique Protocol Identification Number
NCT02128945
Brief Title
Dosimetry and Biodistribution of [18F]-Fludarabine in Lymphoid Malignancies
Acronym
FLUDATEP
Official Title
Dosimetry and Biodistribution of [18F]-Fludarabine in Lymphoid Malignancies
Study Type
Interventional
2. Study Status
Record Verification Date
January 2016
Overall Recruitment Status
Completed
Study Start Date
April 2014 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
May 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Caen
Collaborators
CNRS, UMR ISTCT 6301, LDM-TEP Groupe, GIP Cyceron, Caen, France
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The application of positron emission tomography with lymphoproliferative diseases today provides diagnostic and therapeutic information of major importance , especially in terms of speed and quality of response to treatment. The radiopharmaceutical used in clinical practice for this exam is fluorodeoxyglucose 18F-2-fluoro-2-deoxy-D-glucose fluorodeoxyglucose ([18F]-FDG) . However , the uptake of this tracer is not elective in lymphoid tissues , with a lack of specificity. In addition , the avidity of this tracer is unequal according to the histological subtype (lack of sensitivity).
To try to improve the results of this clinical exploration of lymphoid malignancies, the investigators developed a new radiopharmaceutical ( [18F] - fludarabine ). The idea of transforming the fludarabine radiopharmaceutical is based on the existence of a fluorine atom in the molecule and the pharmacokinetic characteristics of this drug. The [18F]-Fludarabine is a new radiopharmaceutical reproducing the same dosage formulation of fludarabine , a drug used for the treatment of certain types of lymphoproliferative diseases, especially those where the tumor cells have a low proliferation kinetics . This drug is used in therapy in particular pharmacokinetic effect for a high affinity for the lymphoid tissue . Preclinical results on normal and lymphoma xenograft -bearing mice showed a specificity restricted to lymphoid tissue fixation with [18F]-Fludarabine compared with [18F]-FDG .
Based on these encouraging results , the investigators propose in this work to explore the Dosimetry and Biodistribution of [18F] - Fludarabine in human lymphoproliferative diseases : 1)A first group of patients with non-Hodgkin's large cell lymphomas in which it already has a wealth of experience in exploration [18F]-FDG, and 2) a second group of patients with chronic lymphocytic leukemia, where the results of the exploration [18F]-FDG are considered disappointing and did not, for this reason, experienced clinical development.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Untreated B-Chronic Lymphocytic Leukemia or Diffuse Large B Cells Lymphoma Patients
Keywords
PET, Chronic lymphocytic Leukemia (CLL), Diffuse Large B Cells Lymphoma (DLBCL), Fludarabine
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
FLUDATEP
Arm Type
Experimental
Arm Description
[18F] - Fludarabine PET/CT
Intervention Type
Other
Intervention Name(s)
[18F] - Fludarabine PET/CT
Intervention Description
[18F] - Fludarabine PET/CT before treatment
Primary Outcome Measure Information:
Title
Standardized measure of [18F]-Fludarabine uptake in tumor tissue.
Description
Measure of the Standard Uptake Value (SUV) for each lesion.
Time Frame
Day 0 ([18F]-Fludarabine PET-CT day)
Secondary Outcome Measure Information:
Title
Calculation of the equivalent dose to all organs and evaluation of effective dose to the whole body
Time Frame
Day 0 ([18F]-Fludarabine PET-CT day)
Other Pre-specified Outcome Measures:
Title
Distribution and temporal activity curve of [18F]-Fludarabine obtained for each organ and collection of possible adverse events.
Description
Collection of every adverse events
Time Frame
Participants will be followed for a maximum of 9 days after [18F]-Fludarabine PET-CT.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult over 18
Signed written informed consent
Untreated stage B or C chronic lymphocytic leukemia
Untreated diffuse large B-cell lymphoma
Eligible for PET-CT
The subject must be covered by a social security system
Exclusion Criteria:
Age under 18
Patients concurrently included in an investigational trial
Weight over 120 kg
pregnant women
active infectious disease
immune hemolytic anemia
patients with creatinine clearance < 30 ml/mn
corticosteroid therapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sylvain P CHANTEPIE, MD
Organizational Affiliation
University Hospital, Caen
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital
City
Caen
ZIP/Postal Code
14000
Country
France
12. IPD Sharing Statement
Learn more about this trial
Dosimetry and Biodistribution of [18F]-Fludarabine in Lymphoid Malignancies
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