relapsed or rrefractory T cell lymphoblastic acute leukemia/ lymphoma
Conditions
Interventions
dose escalation:CAR-T
dose expansion:CAR-T
Sponsors
Hebei Yanda Lu Daopei Hospital
Eligibility
Sex/Gender
All
Age
2 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. The patient or his guardian understands and voluntarily signs the informed consent form, and is expected to complete the follow-up examination and treatment of the study procedure; 2. Age 2~60 (including threshold), regardless of gender; 3. According to the WHO 2016 standard, the patients with relapsed/refractory acute T-lymphoblastic leukemia/lymphoma (including early pre T-lymphoblastic leukemia) who failed to receive standard treatment or lacked effective treatment methods met any of the following criteria: 1) Recurrence: disease recurrence is confirmed after receiving at least two treatment schemes to achieve complete remission in the past, or disease recurrence occurs after stem cell transplantation to achieve complete remission; 2) Difficult to treat: Have received at least two treatment schemes in the past, and failed to reach CR (for leukemia patients) or PR (for lymphoma patients) after the last treatment, or failed to get remission or develop disease after stem cell transplantation; 4. During screening, the bone marrow examination was definitely diagnosed as CD7 positive by flow cytometry and/or the tumor was definitely diagnosed as CD7 positive by pathological immunohistochemistry, and the positive rate of CD7 was = 70%; 5. Patients who have not received allogeneic hematopoietic stem cell transplantation (allo HSCT) should have the conditions to collect autologous mononuclear cells (hereinafter referred to as blood collection alone) to prepare CAR-T cells. When screening, the peripheral blood smear should show tumor cells<30%; If the patient who has received allo HSCT needs to collect autologous blood, the peripheral blood smear during screening should also show tumor cells<30%. If the donor collects blood alone, there is no such restriction; 6. The patient has recovered from the toxicity of the previous treatment, that is, the CTCAE toxicity grade is less than grade 2 (unless the abnormality is related to the tumor or is judged to be stable by the researcher, which has little impact on the safety or efficacy); 7. The ECOG physical condition score is 0~2 and the expected life span is more than 3 months; 8. Have appropriate organ functions: 1) Glutamic alanine transaminase (ALT) and glutamic oxaloacetic transaminase (AST) = 3 times the upper limit of normal value (ULN). The researcher judges that ALT and AST are abnormal due to diseases (such as liver infiltration or bile duct obstruction), and their indicators can be relaxed to = 5 times ULN; 2) Total bilirubin = 1.5 times ULN; 3) Serum creatinine = 1.5 times ULN, or creatinine clearance = 60 mL/min; 4) Hemoglobin = 70g/L or maintained at this level after blood transfusion; 5) Indoor oxygen saturation = 92%; 6) Left ventricular ejection fraction (LVEF) = 45%.
Exclusion criteria
Exclusion criteria: 1. Have malignant tumors other than T-cell hematological malignancies within 5 years, except for adequately treated cervical carcinoma in situ, basal cell or squamous cell skin cancer, localized prostate cancer after radical resection, breast ductal carcinoma in situ after radical resection cancer. 2. CNS leukemia patients with clinical symptoms. 3. Hepatitis B surface antigen (HBsAg) positive, hepatitis B core antibody (HBcAb) positive; hepatitis C virus (HCV) antibody positive; human immunodeficiency virus (HIV) antibody positive; cytomegalovirus (CMV) DNA test Results = 500 copies/mL; syphilis antibody positive. 4. Those with a history of severe allergies or known any of the active ingredients, excipients or mouse-derived products contained in the drug, or those allergic to xenogeneic proteins in this trial, including lymphocyte depletion regimens. Severe allergy history is defined as an allergic reaction of grade two or above, and any of the following clinical manifestations occur when an allergic reaction occurs: airway obstruction (runny nose, cough, wheezing, dyspnea), hypercardia tachycardia, hypotension, arrhythmia, gastrointestinal symptoms (nausea, vomiting), incontinence, laryngeal edema, bronchospasm, cyanosis, shock, respiration, cardiac arrest. 5. Severe heart disease, including but not limited to severe arrhythmia, unstable angina, massive myocardial infarction, New York Heart Association class III or IV cardiac insufficiency, refractory hypertension (refractory Hypertension is defined as: on the basis of improving lifestyle, a reasonable tolerable and sufficient amount of =3 kinds of antihypertensive drugs (including diuretics) has been used for > 1 month and the blood pressure has not reached the standard, or the blood pressure can only be achieved effective control after taking =4 kinds of antihypertensive drugs. 6. Have unstable systemic disease as judged by the investigator: including but not limited to severe liver, kidney or metabolic disease requiring drug therapy. 7. Those who have received organ transplants or are about to receive organ transplants (except for hematopoietic stem cell transplants). 8. Patients with acute and chronic graft-versus-host disease (GVHD) of any grade after 2 weeks discontinuation of immunosuppressants. 9. Those who have received hematopoietic stem cell transplantation within 6 months before screening. 10. Active autoimmune or inflammatory diseases of the nervous system (eg, Guillain-Barre syndrome (GBS), amyotrophic lateral sclerosis (ALS)) and clinically significant active cerebrovascular disease (eg, cerebral edema) , Posterior Reversible Encephalopathy Syndrome (PRES)). 11. Those who have tumor emergencies (such as spinal cord compression, intestinal obstruction, leukostasis, tumor lysis syndrome, etc.) before screening or reinfusion and need emergency treatment. 12. The presence of an uncontrolled bacterial, fungal, viral or other infection requiring antibiotic treatment. 13. Those who have undergone major surgical operations (except diagnostic surgery and biopsy) within 4 weeks before clearing the lymph cells, or those who plan to undergo major surgery during the study period, or those whose surgical wounds have not healed completely before enrollment. 14. Those who have received (attenuated) live virus vaccine within 4 weeks before screening. 15. Persons with severe mental illness. 16. Those who are alcoholics or have a history of drug abuse. 17. Pr
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| dose limited toxicity, DLT;Maximal Tolerable Dose, MTD;safety index; | — |
Secondary
| Measure | Time frame |
|---|---|
| complete response rate, CRR;partial remission rate, PRR;overall response rate, ORR;duration of remission, DOR;Relapse-Free Survival, RFS;event free survival, EFS;CAR-T in peripheral blood ;Cytokine;Proportion of CD7-positive tumor cells; | — |
Countries
China
Contacts
Public ContactPeihua Lu
Outcome results
None listed