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Tris-CAR-T Cell Therapy for Recurrent Glioblastoma

RecruitingPhase 1Ages 18 Years - 70 YearsAllBeijing Tiantan Hospital
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In plain words

What the trial is, and whether it could suit you

This is a Phase 1 study of recurrent glioblastoma locoregional adoptive therapy with autologous peripheral blood T cells lentivirally transduced to express a dual-target, truncated IL7Ra modified chimeric antigen receptor (CAR), delivered by Ommaya reservoir, a pre-indwelled catheter in the tumor resection cavity or ventricle. Patients with pathological confirmation of glioblastoma and radiological evidence of recurrence are candidates for this clinical trial. If the patient meets all other eligibility criteria, and meets none of the exclusion criteria, will have leukapheresis, and a subsequent Ommaya reservoir implantation. T cells will be isolated from the PBMC sample and then be bioengineered into a 4th generation CAR-T cell, Tris-CAR-T cells. Recipients will be assigned to three courses in the order of enrollment. The first 2 patients will be assigned to the low-dose group. The seco

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📋 Eligibility rules (as published)
Inclusion Criteria: 1. Age: 18 years to 70 years (including cut-off values). 2. Patients with history of glioblastoma are diagnosed with recurrent glioblastoma and residual tumor after intracranial tumor resection/biopsy performed in Beijing Tiantan Hospital. 3. Patients who finished radiotherapy or temozolomide/bevacizumab or other drugs for at least 4 weeks. All toxicities of prior treatment should be defined as less than or equal to grade 1 (except for toxicities such as hair loss or leukoplakia) according to the Common Terminology Standard for Adverse Events (CTCAE 5.0). 4. Patients who is suitable for craniotocerebrospinal fluid shunt and attachment (Ommaya device) implantation confirmed by a competent physician. 5. Patients and/or legal representative is able to sign written informed consent. 6. Kanovsky Performance Status (KPS) ≥ 70. 7. According to the researchers' judgment, the life expectancy ≥ 8 weeks. 8. White blood cells (WBC) \> 3.50×10\^9/L (performed within 14 days prior to PBMC collection unless otherwise noted). 9. Platelet ≥ 200×10\^9/L (performed within 14 days prior to PBMC collection unless otherwise noted). 10. Hemoglobin ≥ 120 g/L (performed within 14 days prior to PBMC collection unless otherwise noted). 11. Total bilirubin ≤ 20 μmol/L (performed within 14 days prior to PBMC collection unless otherwise noted). 12. Aspartic acid aminotransferase (AST) ≤ 2.5×42 U/L (performed within 14 days prior to PBMC collection unless otherwise noted). 13. Alanine aminotransferase (ALT) ≤ 2.5×41 U/L (performed within 14 days prior to PBMC collection unless otherwise noted). 14. Serum creatinine ≤ 90 μmol/L (performed within 14 days prior to PBMC collection unless otherwise noted). 15. Blood oxygen saturation ≥ 95% (performed within 14 days prior to PBMC collection unless otherwise noted). 16. Seronegative of the combination of human immunodeficiency virus (HIV) antibody (Ab) (performed within 14 days prior to PBMC collection unless otherwise noted). 17. Fertile women: a negative serum pregnancy test (performed within 14 days prior to PBMC collection unless otherwise noted). 18. The patient agrees that contraception should be used in patients of childbearing age for at least 3 months from screening to the last infusion of Tris-CAR-T cells. The period of childbearing age is defined as unsurgically neutered (men and women) or without menopause for more than 1 year (women only). Exclusion Criteria: 1. Kanovsky Performance Status (KPS) ≤ 70. 2. Highly allergic constitution or severe allergies history. 3. Those who have psychiatric or psychological diseases and cannot cooperate with treatment and efficacy assessment. 4. Receive other drug trials within 60 days before enrollment, or receive other routine treatment in non-experimental designs for glioblastoma, such as stereotactic radiation therapy or placement of carmustine wafers. 5. Combined with infection, active infection, fever of unknown cause. 6. Combined with serious or unstable heart, lung, liver, kidney and hematopoietic system diseases, including active hepatitis. 7. Combined with inflammation and immune system diseases (such as rheumatoid arthritis), or known immunosuppressive diseases. 8. Combined with neurological diseases, such as diffuse leptomeningeal disease, or neurodegenerative diseases. 9. Known allergies to immunotherapy and related cellular products. 10. Patients who have received any gene therapy before. 11. Long-term use of immunosuppressants is required for any reason. 12. Patients with a history of organ transplantation or who are waiting for organ transplantation. 13. Special cases: pregnancy or lactation. 14. Other circumstances in which the investigators believe the patient is unsuitable for this trial.
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What it tests

  • Inverse correlated dual-target, truncated IL7Ra modified CAR -expressing autologous T-lymphocytes.
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Where

1 site
Beijing Tiantan Hospital
Beijing, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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