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Temporal Characterization of Extracellular Vesicles During Cellular Therapy Using CAR-T Cells and During the Occurrence of Immune Effector Cell-Associated Neurotoxicity Syndrome

Temporal Characterization of Extracellular Vesicles During Cellular Therapy Using CAR-T Cells and During the Occurrence of Immune Effector Cell-Associated Neurotoxicity Syndrome

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06706102
Acronym
VESICANS
Enrollment
60
Registered
2024-11-26
Start date
2025-07-02
Completion date
2027-11-30
Last updated
2025-07-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Immune Effector Cell Associated Neurotoxicity Syndrome

Keywords

CAR-T Cell, ICANS, EVs

Brief summary

Immune effector Cell-Associated Neurotoxicity Syndrome (ICANS) is a common and serious neurological complication associated with the use of CAR-T cells. The mechanisms involved are still poorly understood but studies suggest that inflammation during treatment leads to an increase in the permeability of the barrier between the brain and the blood vessels and the emission of extracellular vesicles (EVs) circulating between the brain and the blood vessels. EVs are biological particles that play an important role in cellular communication and the modulation of several physiological processes. The VESICANS study aims to characterize the EVs released before and during CAR-T cells treatment and upon the occurrence of ICANS, using flow cytometry, electron microscopy, Nanoparticle Tracking Analysis associated with MRI assessment of the barrier between the brain and blood. This study will ultimately contribute to facilitating the prevention and treatment of this toxicity which affects the prognosis of patients.

Interventions

Biological tests : cell quantification et characterization

DIAGNOSTIC_TESTMRI

MRI

DIAGNOSTIC_TESTNeuropsychological tests

Neuropsychological tests

Sponsors

Centre Hospitalier Universitaire de Saint Etienne
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient aged over 18, * Patient for whom CAR-T treatment is indicated, * Patient affiliated to a social security system * Patient who give his consent to participate in the study.

Exclusion criteria

* Pregnant or breastfeeding woman, * Patient unable to understand informed consent, * Patient under legal protection.

Design outcomes

Primary

MeasureTime frameDescription
Endothelial EVs quantification (EVs/mL)Days -7, 0, 1, 2, 5, 8, 15, 30 and 60Quantification by Nano Tracking Analysis of endothelial EVs as a function of time before and after treatment with CAR-T cells according to ICANS grade.
Endothelial EVs characterization (immunophenotyping)Days -7, 0, 1, 2, 5, 8, 15, 30 and 60Characterization by Nano Tracking Analysis (immunophenotyping by size) of endothelial EVs as a function of time before and after treatment with CAR-T cells according to ICANS grade.

Secondary

MeasureTime frameDescription
EVS quantification according to the presence of an ICANS versus no ICANS (EV/mL)Days -7, 0, 1, 2, 5, 8, 15, 30 and 60EVS quantification according to the presence of an ICANS versus no ICANS
EVs characterization according to the presence of an ICANS versus no ICANS (immunophenotyping)Days -7, 0, 1, 2, 5, 8, 15, 30 and 60EVS characterization of EVs according to the presence of an ICANS versus no ICANS
EVs quantification according to levels of cytokines (EVs/mL)Days -7, 0, 1, 2, 5, 8, 15, 30 and 60EVs quantification according to levels of cytokines
EVs characterization according to levels of cytokinesDays -7, 0, 1, 2, 5, 8, 15, 30 and 60EVs characterization according to levels of cytokines
Other EV subtypes quantification (EV subtype/mL)Days -7, 0, 1, 2, 5, 8, 15, 30 and 60Other EV subtypes quantification of as a function of time before and after treatment with CAR-T cells according to ICANS grade.
EVs characterization in cerebrosinalfluid.Days -7, 0, 1, 2, 5, 8, 15, 30 and 60EVs characterization of EVs after treatment with CAR-T cells in cerebrospinal fluid (CSF) if available.
Association of EVs subpopulations in clinical neurological damage and sleep apnea syndrome.Days -7, 0, 1, 2, 5, 8, 15, 30 and 60Characterization of the association of subpopulations of EVs according to clinical neurological damage and sleep apnea syndrome.
Association of EVs subpopulations in neuropsychological test and RMI.Days -7, 0, 1, 2, 5, 8, 15, 30 and 60Characterization of the association of subpopulations of EVs according to neuropsychological test and RMI.
Cerabral involvement on RMIDays -7, 0, 1, 2, 5, 8, 15, 30 and 60Diffusion tensor imaging and resting state default mode network
EVs quantification in cerebrospinal fluid (EVs/mL)Days -7, 0, 1, 2, 5, 8, 15, 30 and 60EVs quantification after treatment with CAR-T cells in cerebrospinal fluid (CSF) if available.
Other EV subtypes characterization (immunophenotyping)Days -7, 0, 1, 2, 5, 8, 15, 30 and 60Other EV subtypes characterization of as a function of time before and after treatment with CAR-T cells according to ICANS grade.

Countries

France

Contacts

Primary ContactEmilie CHALAYER, MD
emilie.chalayer@chu-st-etienne.fr(0)4 77 82 28 14
Backup ContactHélène RAINGARD
helene.raingard@chu-st-etienne.fr(0)4 77 82 97 03

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026