EGFR806-specific CAR T Cell Locoregional Immunotherapy for EGFR-positive Recurrent or Refractory … (NCT03638167) | Clinical Trial Compass
CompletedPhase 1
EGFR806-specific CAR T Cell Locoregional Immunotherapy for EGFR-positive Recurrent or Refractory Pediatric CNS Tumors
United States11 participantsStarted 2019-03-19
Plain-language summary
This is a Phase 1 study of central nervous system (CNS) locoregional adoptive therapy with autologous CD4+ and CD8+ T cells that are lentivirally transduced to express an EGFR806 specific chimeric antigen receptor (CAR) and EGFRt. CAR T cells are delivered via an indwelling catheter into the tumor cavity or the ventricular system in children and young adults with recurrent or refractory EGFR-positive CNS tumors. The primary objectives of this protocol are to evaluate the feasibility, safety, and tolerability of CNS-delivered fractionated CAR T cell infusions employing intra-patient dose escalation. Subjects with supratentorial tumors will receive sequential EGFR806-specific CAR T cells delivered into the tumor resection cavity, subjects with infratentorial tumors will receive sequential CAR T cells delivered into the fourth ventricle, and subjects with leptomeningeal disease will receive sequential CAR T cells delivered into the lateral ventricle. The secondary objectives are to assess CAR T cell distribution within the cerebrospinal fluid (CSF), the extent to which CAR T cells egress into the peripheral circulation, and EGFR expression at recurrence of initially EGFR-positive tumors. Additionally, tumor response will be evaluated by magnetic resonance imaging (MRI) and CSF cytology. The exploratory objectives are to analyze CSF specimens for biomarkers of anti-tumor CAR T cell presence and functional activity.
Who can participate
Age range1 Year – 26 Years
SexALL
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Inclusion criteria
✓. Age ≥ 15 and ≤ 26 years
✓. Histologically diagnosed EGFR positive Central Nervous System (CNS) tumor
✓. Evidence of refractory or recurrent CNS disease for which there is no standard therapy
✓. Able to tolerate apheresis or apheresis product available for use in manufacturing
✓. CNS reservoir catheter, such as an Ommaya or Rickham catheter
✓. Life expectancy ≥ 8 weeks
✓. Lansky or Karnofsky score ≥ 60
✓. If patient does not have previously obtained apheresis product, patient must have recovered from acute toxic effects of all prior chemotherapy, immunotherapy, and radiotherapy and discontinue the following prior to enrollment:
Exclusion criteria
✕. Diagnosis of classic diffuse intrinsic pontine glioma (DIPG)
✕
What they're measuring
1
Safety: any adverse events associated with one or multiple EGFR806-specific CAR T cell product infusions will be assessed by CTCAE v5.0.
Timeframe: up to 6 months
2
Feasibility: The number of successfully manufactured and infused EGFR806-specific CAR T cell product