Clinical Study of Allogeneic Vγ9Vδ2 T Cells in the Treatment of Brain Malignant Glioma

HX-A-2022006-1

Primary brain malignant tumor has become the first lethal tumor in children and young adults, and the treatment is limited, and the prognosis of patients is poor. According to the classification of the World Health Organization, glioblastoma is divided into grade II, III and IV gliomas; The higher the degree of malignancy, the worse the clinical outcome. Among them, the most malignant, most lethal, and most common types of tumors include supratentorial glioblastoma, diffuse endopontine glioma (DIPG), medulloblastoma, and ependymoma. Its high malignancy is mainly manifested in three aspects: extremely rapid growth and obvious invasion; The operation is not easy to remove all; The tumor has a tendency of recurrence and disseminated implantation. It can occur with children and adults of all ages. At present, surgery combined with chemoradiotherapy is the main treatment, but the therapeutic effect is not good. Studies have shown that glioblastoma, as the most common primary brain malignant tumor in adults, after standard surgery, radiotherapy and chemotherapy, the median survival time is less than 15 months, and the overall five-year survival rate is only 5.4%. Even after receiving new and expensive Tumor-treating fields, the median survival time is less than 21 months. The median survival time of DIPG patients is generally less than 1 year, and the 5-year survival rate is less than 5%. The average 5-year survival rate of medulloblastoma and anaplastic ependymoma is 40%\~60%. Innovative treatments are urgently needed. Immunotherapy based on Vγ9Vδ2 T cells has become a promising research direction in recent years. Its unique phosphine antigen recognition does not depend on major histocompatibility complex (MHC), easy to allograft and other advantages. Making it one of the most promising cell therapies. Brain glioma has abnormal cholesterol metabolism and phosphine antigen accumulation, which is easily sensed by Vγ9Vδ2 T cells. Therefore, the clinical exploration of Vγ9Vδ2 T cells for glioma is of great significance to both the scientific and clinical communities.

2024-04-30

2026-12-30

2027-12-30

Not yet recruiting

Early phase I

25

Inclusion Criteria: * Patients with clinically diagnosed malignant brain glioma in an important structural area (WHO Grade IV); * Patients with poor postoperative effect or ineffective guidelines for conventional treatment * Age ≥4 years old, male or female; * KPS score ≥70; * Normal bone marrow reserve function and normal liver and kidney function (as evidenced by the following laboratory tests prior to initial Vγ9Vδ2 T cell therapy) : * Neutrophil absolute value ≥ 1,500/mm3; * hemoglobin 10g/dL; * Platelet count \> 100,000/mm3; * Glutamic pyruvic transaminase/Glutamic oxalacetic transaminase \< 2.5 x ULN; * Serum creatinine 1.5×ULN; * Total bilirubin levels \< 1.5 x ULN. * No obvious genetic diseases; * Normal cardiac function, cardiac ejection index \> 55%; * Suitable for implantation of Ommaya capsule in ventricle or cavity; * No bleeding and coagulation disorders; * Women of reproductive age (15-49 years) must undergo a negative pregnancy test within 7 days before starting treatment and use contraception during the clinical trial period and within 3 months after the last cell transfusion; * Sign the informed consent form. Exclusion Criteria: * Pregnant and lactating women; * Organ failure; * Heart: Grade III and grade IV; * Liver: Level C of the Child-Turcotte liver function scale; * Kidney: renal failure and uremia stage; * Lungs: Symptoms of severe respiratory failure; * Brain: A person with a disorder of consciousness. * Patients with a history of organ transplantation; * Uncontrollable infectious disease or other serious illness, including but not limited to infection (such as HIV positive), congestive heart failure, unstable angina pectoris, arrhythmia, psychosis, or restrictive social environment or what the attending physician considers to be an unpredictable risk; * Patients with systemic autoimmune disease or immunodeficiency; * Patients with allergic constitution; * Use of systemic steroid drugs; * Have a chronic disease that requires the use of immune agents or hormone therapy; * Prior treatment with any other immune cell; * Have participated in other clinical trials within the past 30 days; * The researchers believe that other reasons are not suitable for clinical trials

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2024-05-02