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Phase 1 Study of Autologous Anti-EGFRvIII synNotch Receptor Induced Anti-EphA2/IL-13R alpha2 CAR (E-SYNC) T Cells in Adult Participants With EGFRvIII+ Glioblastoma

Status: Recruiting
Location: See location...
Intervention Type: Biological, Drug, Procedure
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

This phase I trial tests the safety, side effects, and best dose of E-SYNC chimeric antigen receptor (CAR) T cells after lymphodepleting chemotherapy in treating patients with EGFRvIII positive (+) glioblastoma. Chimeric antigen receptor (CAR) T-cell therapy is a type of treatment in which a patient's T cells (a type of immune system cell) are changed in the laboratory so the CAR T cells will attack cancer cells. T cells are taken from a patient's blood. Then the gene for a special receptor that binds to a certain protein on the patient's cancer cells is added to the T cells in the laboratory. The special receptor is called a chimeric antigen receptor. Large numbers of the CAR T cells are grown in the laboratory and given to the patient by infusion for treatment of certain cancers. Lymphodepleting chemotherapy with cyclophosphamide and fludarabine before treatment with CAR T cells may make the CAR T cells more effective.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Inclusion Criteria for Cohort 1:

‣ Age \>= 18 years.

⁃ Karnofsky performance status (KPS) score of \>=70.

⁃ All participants must have adequate organ function defined as:

• Peripheral absolute neutrophil count \>=1000/mm\^3.

∙ Platelet count \>=100,000/mm\^3 (transfusion independent, defined as not receiving platelet transfusions for at least 7 days prior to enrollment).

∙ Absolute lymphocyte count (ALC) \>= 300/μL and/or Cluster of differentiation 3 (CD3) count of \>=150/μL.

∙ Creatinine clearance or radioisotope glomerular filtration rate \>= 50 mL/min/1.73m\^2.

∙ Total Bilirubin \<= 1.5 x ULN except for Gilbert's syndrome and

∙ Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) \<= 3x upper limit of normal (ULN).

∙ Left ventricular ejection fraction (LVEF) \>= 50% by echocardiogram or multi-gated acquisition scanning (MUGA).

∙ Adequate pulmonary function, defined as no evidence of dyspnea at rest and pulse oximetry \> 92% while breathing room air.

⁃ Pathological criteria: EGFRvIII+ GBM from most recent surgery, confirmed by a Clinical Laboratory Improvement Amendments (CLIA)-certified lab using a next-generation sequencing panel.

⁃ MGMT promoter must be unmethylated or with a methylation index \< 3.

⁃ Must have completed at least standard of care (SOC) external beam radiotherapy (EBRT) as initial therapy.

⁃ Participants must be anticipated to be able to complete E-SYNC T cell infusion within 12 weeks after completion of EBRT.

⁃ All participants must be off systemic steroids for 3 days or more prior to leukapheresis.

⁃ Must be willing to provide voluntary informed consent for apheresis (and tissue screening if needed) and for study treatment.

⁃ NOTE: There are two sets of eligibility criteria for Cohort 2. Tissue Screening: Defines eligibility for tissue screening and to determine H-score.

⁃ Study Enrollment: Defines eligibility for study enrollment and E-SYNC T cell manufacturing/treatment.

• Inclusion Criteria for Tissue Screening Cohort 2:

‣ Age \>=18 years.

⁃ Pathological criteria: EGFRvIII+ GBM from most recent surgery, confirmed by a Clinical Laboratory Improvement Amendments (CLIA)-certified lab using a next-generation sequencing panel.

• Inclusion Criteria for Study Enrollment for Cohort 2

‣ Karnofsky Performance Scale (KPS) score \>=70.

⁃ received at least standard of care external beam radiotherapy (SOC EBRT) as initial therapy, with or without concurrent temozolomide (TMZ), and completed the last dose of TMZ ≥23 days prior to study enrollment). Note: patients may have initiated adjuvant TMZ +/- TTFields.

⁃ Pathological criteria: EGFRvIII+ GBM from most recent surgery, as defined by an EGFRvIII H-score of ≥ 150 based on central review.

⁃ Is surgically amenable, with expectation for ability to resect at least 500 mg of tumor tissue confirmed by participant's neurosurgeon.

⁃ Participants with reproductive potential agree to use reliable and double barrier method of contraception during the study and for at least 6 months after the last study intervention, including refraining from donating sperm during this period.

⁃ Females of childbearing potential must have a negative serum beta-human chorionic gonadotropin (HCG) pregnancy test prior to receiving study interventions.

⁃ All participants must have adequate organ function.

‣ a. Adequate bone marrow function is defined as: i. Peripheral absolute neutrophil account ≥ 1000/mm3 and ii. Platelet count ≥ 100,000/mm3 (transfusion dependent, defined as not receiving platelet transfusions for at least 7 days prior to enrollment) and iii. Absolute lymphocyte count (ALC) ≥ 300/µL and/or CD3 count of ≥ 150/µL b. Adequate renal function is defined as: i. Creatinine clearance or radioisotope glomerular filtration rate ≥ 50 mL/min/1.73m2 c. Adequate liver function is defined as: i. Total Bilirubin ≤ 1.5 x upper limit of normal (ULN) except for Gilbert's syndrome and ii. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3 x ULN d. Coagulation tests prothrombin time (PT) and partial thromboplastin time (PTT) have to be within normal limits, unless the participant has been therapeutically anti-coagulated for previous venous thrombosis. e. Adequate pulmonary function, defined as no evidence of dyspnea at rest and pulse oximetry \> 92% while breathing room air.

‣ f. Adequate cardiac function, confirmed within the last 12 months, defined as: i. Left ventricular ejection fraction (LVEF) ≥ 40% by echocardiogram or multi-gated acquisition scanning (MUGA)

⁃ Must be willing to provide voluntary informed consent for study intervention.

Locations
United States
California
University of California, San Francisco
RECRUITING
San Francisco
Contact Information
Primary
Neuro-Oncology New Patient Coordinator
NeuroOncNewPatientCoord@ucsf.edu
877-827-3222
Time Frame
Start Date: 2024-04-30
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 20
Treatments
Experimental: Cohort 1: Starting Dose Level 1 (5 x 10^7 CAR+ cells) (DL1)
Participants with newly diagnosed EGFRvIII+ GBM with unmethylated MGMT promotor status will undergo leukapheresis for manufacturing of E-SYNC T cells at least 2 weeks after completion of non-interventional, standard of care radiation therapy. Participants receive cyclophosphamide IV and fludarabine IV on days -5, -4, and -3 and then receive E-SYNC T cells IV on day 0. Participants will receive a single infusion of drug product (DP) (5 x 10\^7 CAR+ T cells) and be monitored for safety, presence of and possible synNotch \> CAR-T priming of the DP in the peripheral blood.
Experimental: Cohort 1: Dose-escalation Level 2 (1.5 x 10^8 CAR+ cells) (DL2)
If there are no dose-limiting toxicities in the starting dose cohort, participants with newly diagnosed EGFRvIII+ GBM with unmethylated MGMT promotor status will undergo leukapheresis for manufacturing of E-SYNC T cells at least 2 weeks after completion of tnon-interventional, standard of care radiation therapy. Participants receive cyclophosphamide IV and fludarabine IV on days -5, -4, and -3 and then receive E-SYNC T cells IV on day 0. Participants will receive a single infusion of drug product (DP) (1.5 x 10\^8 CAR+ T cells) and be monitored for safety, presence of and possible synNotch \> CAR-T priming of the DP in the peripheral blood.
Experimental: Cohort 2: Tissue analysis cohort
Participants with EGFRvIII+ glioblastoma and residual disease appropriate for surgery will have EGFRvIII H-score assessed by digital image analysis of Immunohistochemistry (IHC) slides from the initial surgical sample, reflecting staining extent and intensity. Participants with H-score ≥150 who underwent initial tumor resection, completed non-investigational standard-of-care radiation therapy, and meet eligibility criteria will undergo leukapheresis to manufacture E-SYNC T cells at the maximum tolerated or recommended dose based on Cohort 1 results. Participants will receive lymphodepleting conditioning followed by a single drug product (DP) infusion on Day 0. After platelet recovery, participants will be hospitalized for non-investigational surgical resection approximately 2 weeks after DP infusion. Participants will be monitored for safety, DP synNotch \> CAR-T priming, and anti-tumor response of E-SYNC T cells.
Sponsors
Collaborators: California Institute for Regenerative Medicine (CIRM), National Cancer Institute (NCI)
Leads: Hideho Okada, MD, PhD

This content was sourced from clinicaltrials.gov