Immunotherapy With CD19 CART-cells for B Cell Acute Lymphoblastic Leukemia
Leukemia, B-Cell
About this trial
This is an interventional treatment trial for Leukemia, B-Cell focused on measuring Chimeric Antigen Receptor-Modified T Cells, CART, Recurrent B Cell Acute Lymphoblastic Leukemia, refractory B Cell Acute Lymphoblastic Leukemia, ALL
Eligibility Criteria
Inclusion Criteria:
- Recurrent or refractory B cell derived acute lymphoblastic leukemia (ALL)
- Patients who have failed at least one line of a standard treatment without effective treatment measures at present
- CD19 expression on the surface of B-ALL cells must be detected
- KPS>80
- Life expectancy >3 months
- Patients must have adequate cardiac function (no electrocardiogram with obvious abnormality, LVEF≥50%),adequate pulmonary function as indicated by room air oxygen saturation of > 90%, and adequate renal function (Cr≤2.5 times of the normal range)
- The alanine aminotransferase (ALT) and the aspartate aminotransferase (AST)≤ 3 times of the normal range, and the total bilirubin (TBIL)≤2.0mg/dl(34.2umol/L)
- Hemoglobin(Hgb)≥80g/L
- Without contraindication of apheresis and cell isolation
- Patients and their families volunteer to participate in the research with signed written informed consent
Exclusion Criteria:
.Other concurrent severe and/or uncontrolled medical conditions: patients with another primary malignant disease; another severe and/or life-threatening medical disease.
- Evidence of uncontrolled current serious active infection
- HIV/HBV/HCV infection
- Pregnancy and nursing females
- Systemic glucocorticoid therapy within one week
Sites / Locations
Arms of the Study
Arm 1
Experimental
B-ALL treated with CD19 CART cell
The qualified CD19-targeted CART cells will be transferred to patient for 3 days as follow:D1,10% fraction;D2,30%;D3 60%. The number of CART cells for each course will be about 1×106/kg. If complete response (CR) or complete response with incomplete hemogram recovery (CRi) in hemogram is achieved after the first course of treatment, further treatment will be decided according to the clinical assessment and the wishes of the patient.If partial response (PR) is achieved after the first course, 1 or 2 courses of treatment will be continued. If there is no response (NR) after the first course, the treatment will be ceased or restarted based on the clinical assessment or patients' wishes. Treatent may be discontinued due to any severe toxicity, such as cytokine release syndrom.