Tracking Peripheral Blood Mononuclear Cells With Fluorine MRI

Adverse Reaction to Diagnostic Agents and Kits Nos Clinical Trial

— TRACK  

Official title:

A Phase I Study Evaluating the Feasibility of Using Fluorine-19 Cell Sense to Image Human Peripheral Blood Mononuclear Cells In Vivo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT02921373
• Other study ID #: CS-PBMC-2015-001
• Status: Not yet recruiting
• Phase: Phase 1
• Start date: July 2019
• Est. completion date: December 2022

Study information

• Verified date: May 2018
• Source: Western University, Canada
• Contact: Gregory A Dekaban, PhD
• Phone: 519-931-5777
• Email: dekaban[@]robarts.ca
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Cell-based therapies in the form of stem cell-based or immune cell-based therapies are becoming important treatment options that are either approved for clinical use or are showing promise in clinical trials. One of the issues regarding cell-based therapies is that, once the cells are injected into a subject, there is no easy way to track where they go, assess whether adequate numbers of cells arrive at the intended therapeutic target and for how long they persist at a given location. To address this issue non-invasive imaging methods have been developed using magnetic resonance imaging (MRI). When used with an appropriate cell labelling contrast agent, Cellular MRI can track cells non-invasively in vivo. Detection of cells is accomplished with an inert imaging agent containing the MRI sensitive fluorine-19 (19F) nuclei. The objective of this study is to demonstrate that 19F-MRI is safe to use in humans so that it can subsequently be used to track cell-based immunotherapies in future clinical trials. The long term goal is to be able to quantify immune cell migration to secondary lymphoid tissues and potentially to tumors and correlate to therapeutic outcomes.

Description:

Background: None of the currently available Good Manufacturing Practices (GMP)-grade MRI cell labelling agents are approved for use in Canada. There is one iron oxide nanoparticle GMP grade preparation that is commercially available but it is not suitable for labelling the immune cell populations the investigators are interested in tracking in vivo. The investigators have, instead, chosen to develop the commercially available, GMP-grade 19F-based perfluorocarbon, known as Cell Sense, for the purpose of tracking immune cell-based vaccine therapies in vivo. This agent has been successful used in a phase I clinical trial in United States and is approved for a second trial current recruiting, under the oversight of the FDA.

The cell tracing agent Cell Sense (CS-1000) is an inert, non-metabolizable tracer. As CS-1000 is taken-up and incorporated into the cell traditional pharmacodynamic and pharmacokinetic analyses in animals and humans are not appropriate, as adsorption and biodistribution will vary with cell type, and therefore have not been done. In vitro studies of toxicity towards various cell types did not yield evidence of adverse effects on various cell functions. Cell Sense also was shown to be non-mutagenic using the Ames and Forward thymidine kinase (TK) assays. Some limited skin irritation was observed when >2,500 fold more Cell Sense than expected to be maximally injected into humans was injected intradermally into rats.

Examples of MRI cell tracking labels include superparamagnetic iron oxide nanoparticles and 19F-containing compounds such as perfluorocarbons. The advantage of using cellular MRI to track cells is that a non-radioactive tracer is used that is suitable for longitudinal studies. MRI offers 3D imaging with exquisite soft tissue contrast. The additional advantage of using 19F over iron-based agents is that 19F is a positive, easily quantifiable contrast cell labelling agent. Furthermore, there is no 19F-background MRI signal in humans whereas MRI involving iron can be confounded by different imaging artifacts and it is a negative contrast agent that is difficult to accurately quantify. The investigators are particularly interested in whether immune cells arrive in secondary lymphoid organs such as lymph nodes.

Study Design:

Open label, dose escalating, single centre, phase I study that will accrue (a) 6 healthy adults and (b) 6 prostate cancer patients.

Three healthy adults and three prostate cancer patients will be enrolled into the first cohort. Whole blood (150 ml) will be obtained by venipuncture. After processing of the blood to obtain peripheral blood mononuclear cells (PBMC), half of the PBMC will be treated with Cell Sense for 8-24 hours. Given the robustness of our data using 5 donors during dry runs, the investigators do not propose to compare labeled vs unlabeled cells as release criteria. However, the investigators will be collecting this data for information and research purposes. Three million (3 x 106) Cell Sense labeled autologous PBMC will be administered intradermally to the cohort 1 subjects. The three healthy adults and the 3 prostate cancer subjects will be tested concurrently.

If no grade 2 or higher adverse events are observed with the 1st cohort, concurrent enrolment will proceed to recruit a second set of 3 healthy adult subjects and the second set of 3 prostate cancer patients. The second cohort of subjects will be subjected to the same design but with an escalation of the dose to 2-3 x 107 Cell Sense-labeled autologous PBMC administered intradermally.

Endpoints:

Primary Endpoints:

Determine the feasibility of using Cell Sense to detect and monitor the migration of PBMC in humans

Secondary Endpoints:

• Confirm and further optimize the 19F Cell Sense detection and Hydrogen- 1 (1H) anatomical imaging parameters for imaging using the 19F/1H dual coil.

• Determine if Cell Sense-labeled PBMC migration to the draining lymph node can be detected.

• Determine if the lymph nodes in the area of interest imaged change in size on the injected side compared to the contralateral side.

• Quantify the number of Cell Sense-labeled PBMC detected.

• Evaluate safety parameters (toxicity) as defined by:

• adverse events.

• serious adverse events.

• changes in laboratory determination and vital sign parameters as assessed by medical history, physical examination and clinical laboratory tests.

The following categories will be used to grade any adverse events:

• Grade 1: does not interfere with daily activity,

• Grade 2: interferes with daily activity, no treatment required, except paracetamol,

• Grade 3: prevents daily activity or requires treatment.

• Grade 4: Life-threatening

NIH and FDA (or CTCAE v 4.0) guidelines will be used to determine the severity of adverse events

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 12
• Est. completion date: December 2022
• Est. primary completion date: June 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 40 Years to 85 Years

Eligibility

Inclusion Criteria:

• Men diagnosed with confirmed adenocarcinoma of the prostate

• No history of skin hypersensitivities or allergies.

• Normal liver functions as defined by alanine aminotransferase (ALT) (3-36 U/L) and aspirate aminotransferase (AST) levels (10-34 U/L)

• Normal kidney function by monitoring urea (2.5-8.0 ?mol/L) and creatine (70-120 µmol/L [for males]) concentrations.

• Normal complete blood count with differential

• Body Weight between 40 and 110 kg (relates to being able to fit in scanner)

• Body Mass Index < 30 (relates to being able to fit in scanner)

• Negative for (HIV, HTLV1&2, Hep A, B, C, syphilis) infection as determined by approved serological testing.

Exclusion Criteria:

• Contraindication to venipuncture and donation of 100-160 mL of blood

• Active infection (not limited to HIV, HTLV1&2, Hep A, B, C, syphilis)

• Participants are on active chemotherapy (not including castrate hormone therapy), radiation therapy or immunosuppressive therapy (i.e. steroid use, anti-transplant rejection drugs, depleting antibodies)

• Participants who are unable to have an MRI scan (e.g. history of head or eye injury involving metal fragments, implanted electrical device (such as a cardiac pacemaker), conductive implants or devices such as skin patches, body piercing or tattoos containing metallic inks, severe heart disease (including susceptibility to heart rhythm abnormalities), claustrophobia, etc.)

• Participants with known allergies to phenol red, ß-lactams and ß-lactam derivative

• Participants with known allergies to streptomycin sulfate and gentamicin sulfate

• Participants with unforeseen conditions that are deemed unsafe or inappropriate for the study (e.g. participants who are claustrophobic and cannot undergo an MRI) as per the discretion of the principal investigator.

Related Conditions & MeSH terms

• Adverse Reaction to Diagnostic Agents and Kits Nos

Intervention

Biological:
• 19F Cell Sense-labeled PBMC
Peripheral blood mononuclear cells (PBMC) will be isolated from patient whole blood samples and labeled in a GMP facility with GMP grade 19F Cell Sense imaging agent. These cells will be re-administered to the patient prior to imaging.

Device:
• MRI
Participants will undergo Magnetic Resonance Imaging (MRI) at 1 hour and 24 hours following PBMC administration

Locations

Country	Name	City	State
Canada	Robarts Research Institute	London	Ontario

Sponsors (3)

Lead Sponsor	Collaborator
Gregory A. Dekaban	Ontario Institute for Cancer Research, University of Western Ontario, Canada

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants with treatment-related adverse effects as assessed by CTCAE v4.0		12 months
Secondary	Number of patients with detectable 19F MRI signal at the site of injection	This process will involve testing if the number of PBMC at the site of injection can be visualized and quantified following injection. Signal produced by labeled cells is linearly related to the number of cells. In vivo quantification has been demonstrated in animal modes, but not in a clinical setting to date.; If necessary, specific imaging parameters will be adjusted to optimize for clinical anatomical and 19F cell tracking imaging.	1hr post injection
Secondary	Number of patients with detectable 19F MRI signal at local lymph nodes	PBMC are required to migrate to the lymph node for optimum therapeutic effect. Here the investigators will determine if 19F-MRI contains the necessary imaging sensitivity to detect migration.	24 hours post injection