Efficacy Study About Donor Derived CD19-target T Cell to Treat B-ALL Post Hematopoietic Stem Cell Transplantation
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- ORR at 6 month
研究概览
简要总结
Efficacy study about donor derived CD19-target T cell to treat B-ALL post hematopoietic stem cell transplantation
详细描述
Allogeneic hematopoietic stem cell transplantation (allo-hsct) for the treatment of refractory recurrent acute b-lymphoblastic leukemia (b-all), the overall survival rate of 3 years after transplantation was about 10%. The overall survival rate at 3 years was about 70 percent. In the early stage, the investigators established the monitoring method of leukemia micro-residual disease, effectively screened out the high-risk group of recurrence, combined with the new relapse treatment method, successfully implemented the stratification and even personalized dry prediction of leukemia recurrence for the first time in the world, and reduced the recurrence rate of the high-risk group by 30%. However, the therapeutic targeting is not strong, and up to 30% of patients will develop graft versus host disease, which seriously affects the survival of patients. The use of CAR repair T cells (CAR T) to target CD19 in the treatment of refractory recurrent b-all was effective, and the use of CAR T in the treatment of recurrent b-all after transplantation did not increase the risk of GVHD. This clinical study mainly discussed the safety and efficacy of donor targeted cd19-t cells after allo-hsct in the treatment of acute b-lymphocytic leukemia with minimal residual disease. It is expected that the recurrence rate will be reduced while the incidence of acute GVHD after transplantation will not be increase
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 3 Years 至 65 Years（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •To be aged 3 to 65 years
- •It was consistent with the diagnosis of CD19+ B-All with MRD+ in allo- hsct transplantation
- •The immunotyping was determined to be CD19+ B-All
- •The T lymphocytes in the subjects were 100% donor T lymphocytes
- •No chemotherapy or antibody treatment was received 2 weeks before cell therapy
- •Left ventricular ejection fraction (LVEF) ≥50% and centerless inclusion were diagnosed by echocardiography
- •The subjects had no pulmonary active infection
- •Blood oxygen saturation at the fingertips ≥ 92%
- •Estimated survival of >3 months
- •ECOG physical condition level 0~1
排除标准
- •Unwilling to accept IM19 CAR-T cell therapy, do not agree to signInformed consent of subject
- •Subjects are allergic to the components of cellular products
- •Total serum bilirubin ≥ 2.0mg/dl、Serum albumin < 35g/L、ALT and AST were more than 3 times of the upper limit of the normal range. Blood creatinine ≥ 2.0mg/dl;Platelet < 20 x 109 / L
- •Subjects had activity level II-IV aGVHD, or activityModerate to severe cGVHD
- •The subjects had a severe failure to control the infection
- •Subject with known central nervous system leukemia (CNS2 or CNS3)
- •Subjects were treated with CAR T cells or DLT after transplantation
- •The subjects developed bone marrow failure syndrome after allo-hsct transplantation
- •The subjects had previously received other gene treatments
- •The subjects had a history of alcohol, drug use or mental illness
- •Subjects were enrolled in any other clinical investigator within 1 month prior to screening
- •Female subjects: 1) were pregnant/lactating, or 2) had a pregnancy plan during the study period,Or 3) fertile and unable to use effective contraception
- •The researchers believe there are other conditions that may not be appropriate for the study
结局指标
主要结局
ORR at 6 month
时间窗: 6 months
Objective response at 6 month
次要结局
未报告次要终点