Refractory B-cell Acute Lymphoblastic Leukemia, Childhood, Relapsed B-cell Acute Lymphoblastic Leukemia, Childhood, Relapsed/Refractory B-cell Lymphoma, Childhood
Conditions
Brief summary
This is a single arm, open-label, uni-center, phase I study . In this study, Children withCD19+/CD22+ R/R B-cell acute lymphoblastic leukemia or lymphoma will be treated with CAR-T19/CAR-T22 Immunotherapy to determine the safety and efficacy of treatment.
Interventions
BIOLOGICALCAR-T19/CAR-T22
According to tumor burden and other conditions, patients will be treated with cyclophosphamide or fludarabine,then,CAR-T cells will be infused 48-72 hours later.The recommand dose is 1x10\^5/kg-2.5x10\^8/kg .
Sponsors
Xiangya Hospital of Central South University
Shenzhen BinDeBio Ltd.
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
1 Months to 18 Years
Healthy volunteers
No
Inclusion criteria
* Male and female subjects with CD19+/CD22+ B cell malignancies who have limited prognosis (several months to \< 2 year survival) with currently available therapies will be enrolled. 1. no available curative treatment options (such as autologous or allogeneic SCT) 2. If patients had receive immunotherapy, they should reach requirments:tumor recurrency or the number of B cells recovered. 3. Patients with recurrence after hematopoietic stem cell transplantation need additional satisfaction: 1) no GvHD and not require immunosuppression;2) stem cell transplantation was completed for at least 4 months, and at least 6 months before the CART reinfusion; 4. Patients must be willing to sign an informed consent. 5. Age:≤18 years. 6. survival\>12 weeks 7. Flow cytometry or IHC showed positive expression of CD19/ CD22 in tumor cells within two months. 8. Routine blood test:hemoglobin\>=90 g/L; platelet\>=50×10\^9/L. 9. Liver function: ALT and AST≤2.5 (ULN) times the upper limits of normal (if abnormal liver function is mainly caused by tumor infiltration, it can ≤5 ULN), bilirubin \<2.0 mg/dl. 10. Renal function:BUN: 9-20mg / dl; serum creatinine\<= 1.5 times upper limits of normal; endogenous creatinine clearance rate\>=50 ml/min 11. Negative serum antibody for EBV, CMV, HIV , syphilis, HBVa nd HCV. 12. Cardiac function: stable hemodynamic and left ventricular ejection fraction (LVEF)\>=55%. 13. ECOG score ≤2。 14. Adequate venous access for apheresis, and no other contraindications for leukapheresis
Exclusion criteria
1. ECOG \>= 3. 2. Patients with history of T cell tumors . 3. organ failure:heart failure Ⅲ and Ⅳ;The liver reached grade C of child-turcotte .Renal failure and uremia;Respiratory failure;People with impaired consciousness. 4. Acute or chronic GVHD after allogeneic hematopoiesis. Hormone or immunosuppressant was used within 30 days. 5. steroid hormoneswere used before and after blood collection and infusion. 6. HIV infection or active hepatitis B or hepatitis C infection. 7. Uncontrolled active infection. 8. Enrolled to other clinical study in the last 4 weeks. 9. Subjects with systemic auto-immune disease or immunodeficiency. 10. Allergic to cytokines. 11. Definite neuropathic or psychotic patients, including authors of dementia or seizures, history of psychotropic substance abuse and unable to quit, or other substantial lesions that may increase central neurotoxicity. 12. Patients with malignant tumors of the central nervous system. 13. Lung, brain or intestinal tumor infiltrates. 14. The second tumor was found. 15. Allergic to cytokine antagonists. 16. Other patients that researchers considered unsuitable for inclusion.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants With Adverse Events evaluated with NCI CTC AE, version 4.0 | 60 months | Safety evaluation |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Overall remission rate | 60 months | Overall remission rate consists of complete remission rate and partial remission rate of patients being treated with CAR-T19/CAR-T22 |
| CAR-T cells testing | 60 months | The level of CAR-T cells will be tested regularly by Real-time Quantitative Polymerase Chain Reaction Detecting System(qPCR) or Flow cytometry to evaluate the proliferation in vivo and long-term survival. |
Countries
China
Contacts
Primary ContactYang Zhonghua
Outcome results
None listed