Clinical Study on the Treatment of Malignant Brain Glioma by QH104 Cell Injection

Dushu Lake Hospital Affiliated to Soochow University

Status and phase

Enrolling

Phase 2

Phase 1

Conditions

Brain Gliomas

High-Grade Gliomas

GBM

Treatments

Biological: Allogenic B7-H3 CAR-γδT cell(QH104)

Study type

Interventional

Funder types

Other

Identifiers

NCT06018363

QH10401-GC-01（0）

Details and patient eligibility

About

B7-H3 is expressed at low levels in normal tissues but overexpressed in various tumor tissues. The ubiquitous expression of B7-H3 in tumors of different grades is a key feature for brain gliomas. The immunohistochemistry study showed that B7-H3 is abundantly expressed on both glioma (especially high-grade glioma) cells and tumor-associated endothelial cells. For GBM, the expression of B7-H3 is intensely positive, especially on tumor cells and vascular endothelial cells, which makes B7-H3 a potential immunotherapeutic target.

γδ T cells recognize tumor cells without being restricted by MHC molecules, and thus can be used in allogeneic therapy without the risk of causing graft-versus-host disease.

This study is an open-label, single-arm, dose-escalation and dose-expansion clinical study aimed at evaluating the safety and efficacy of allogeneic B7-H3 CAR γδT in patients with malignant glioma.

Enrollment

25 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

1)Age 18-70 years old (both ends included), both male and female;
2)At least one evaluable lesion, with previous biopsy or histopathological confirmation of high-grade glioma (WHO grade 3-4), and after comprehensive treatment, imaging examination indicates continued progression or recurrence;
1. The pathological tissues removed by surgery can be used for immunohistochemical detection of target proteins (paraffin sections should be within half a year), and the expression of B7-H3 is positive;
1. KPS ≥ 60 points;
5)Expected survival > 3 months;
6)Substantially normal bone marrow reserve function and normal liver and renal function (laboratory tests need to be fulfilled before receiving QH104 Cell Injection for the first time):White blood cell count (WBC) ≥ 3 x 10^9/L;Lymphocyte count (LY) ≥ 0.8 x 10^9/L;Hemoglobin (Hb) ≥ 90g/L;Platelet (PLT) ≥80×10^9/L;Albumin transaminase (ALT) & albumin transaminase (AST) <1.5×ULN;Serum creatinine (Cr) <1.5 x ULN;Total bilirubin < 1.5 x ULN;PT & PTT ≤ 1.25 x ULN.
7)No obvious hereditary diseases;
8)Normal cardiac function with cardiac ejection index >55%;
9)No bleeding and coagulation disorders;
10)Women of childbearing age (15-49 years old) must have had a pregnancy test with a negative result within 7 days prior to the start of treatment, and subjects are willing to use contraception during the clinical trial and for 3 months after the last cell infusion;
1. Sign the informed consent form.

Exclusion criteria

1)Pregnant and lactating women;
2)Those with organ failure:Heart: Class III and IV;Liver: up to grade C of the Child-Turcotte Liver -Function Classification;Kidney: chronic kidney disease stage 4 or above; renal insufficiency stage III or above;Lungs: symptoms of severe respiratory failure with involvement of other organs;Brain: central nervous system abnormalities or impaired consciousness;
3)patients with combined second tumors;
4)patients with active hepatitis B or C virus, HIV infection, or other untreated active infection;
5)any severe, uncontrolled systemic autoimmune disease or any unstable systemic disease, including but not limited to systemic lupus erythematosus, rheumatoid arthritis, ulcerative colitis, Crohn's disease, and temporal arteritis;
6)Current systemic use of steroid cell (except for recent or current use of inhaled steroids) substances;
1. have a chronic disease requiring immunologic or hormonal therapy;
1. have an allergy to immunotherapy and related cells;
1. 10)Patients with a history of organ transplantation or who are awaiting organ transplantation;
10)Participation in other clinical trials within the previous 30 days;
11)Those who are not suitable for clinical trials for other reasons in the opinion of the investigator.