Exploratory Study of CD22/CD19 Dual-Target CAR-T Cell Therapy as Consolidation Treatment After First Remission in High-Risk B-Cell Acute Lymphoblastic Leukemia
An Exploratory Study on Targeted CD22/CD19 Chimeric Antigen Receptor (CAR)-T Cell Immunotherapy for Enhanced Consolidation Therapy After Initial Remission in High-risk B-cell Acute Lymphoblastic Leukemia
研究概览
研究类型
注册 (估计的)
阶段
- 阶段2
- 阶段1
联系人和位置
学习联系方式
- 姓名:Li-Ping Dou, Dr.
- 电话号码:+8613681207138
- 邮箱:lipingruirui@163.com
学习地点
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Beijing Municipality
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Beijing、Beijing Municipality、中国、100853
- 招聘中
- Chinese PLA General Hospital
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Patients who have provided written informed consent and are willing and able to comply with study procedures, including scheduled visits, treatment, laboratory tests, and other study-related assessments.
- Patients with cytologically or histologically confirmed B-cell acute lymphoblastic leukemia/lymphoma (B-ALL/LBL) according to WHO 2022 criteria, with CD19-positive and/or CD22-positive disease. Patients must have achieved first morphological complete remission (CR1; bone marrow blasts <5%) after standard induction chemotherapy. Patients may or may not have achieved deep remission, defined as minimal residual disease (MRD) negativity assessed by flow cytometry and/or molecular methods (e.g., quantitative PCR or next-generation sequencing).
Patients who are eligible for enhanced consolidation therapy. Patients with high-risk disease defined as:
High-risk group based on cytogenetic and molecular features, regardless of MRD status after consolidation; or Standard-risk group with persistent MRD positivity after two cycles of consolidation therapy, indicating a high risk of relapse.
In addition, patients are unwilling or ineligible to allogeneic hematopoietic stem cell transplantation, and are planned to receive CAR-T cell therapy as consolidation treatment.
- Age between 18 and 85 years, regardless of sex.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
- Estimated life expectancy ≥3 months.
- Hemoglobin ≥60 g/L (transfusion allowed).
- Absolute neutrophil count ≥1,000/μL and platelet count ≥45,000/μL.
Adequate organ function, defined as:
Total bilirubin ≤1.5 × upper limit of normal (ULN) (except Gilbert's syndrome); ALT and AST ≤2.5 × ULN; Serum creatinine ≤1.5 × ULN or creatinine clearance ≥60 mL/min (Cockcroft-Gault formula); Left ventricular ejection fraction (LVEF) ≥50%, no clinically significant arrhythmia, and no pericardial effusion; Baseline oxygen saturation >92% on room air; No clinically significant pleural effusion.
- Subjects of reproductive potential must agree to use effective contraception from enrollment until at least 6 months after completion of the study. Subjects who are pregnant or suspected to be pregnant must notify the investigator immediately.
Exclusion Criteria:
Patients with relapsed/refractory B-cell acute lymphoblastic leukemia (B-ALL), or with risk factors indicating the need for allogeneic hematopoietic stem cell transplantation (meeting any of the following), who are planned to receive allogeneic hematopoietic stem cell transplantation or CD19/CD3 bispecific antibody (blinatumomab) therapy and refuse CAR-T cell immunotherapy as consolidation treatment, including any of the following conditions:
① Early relapse within 6 months after achieving first complete remission;
② Primary refractory disease, defined as failure to achieve first morphological complete remission after two cycles of standard first-line induction chemotherapy;
③ Failure to achieve complete remission or relapse after first-line or multiple lines of salvage chemotherapy;
④ Relapse after allogeneic hematopoietic stem cell transplantation.
- Prior treatment with any CAR-T cell therapy or other genetically modified T-cell therapies.
Known history of HIV infection, active hepatitis B virus (HBV) infection, or any uncontrolled active systemic infection requiring intravenous antibiotics.
(Active HBV infection is defined as: HBV DNA ≥2000 IU/mL, ALT ≥2×ULN, and exclusion of other causes of hepatitis.)
Non-disease-related hepatic or renal dysfunction defined as:
ALT or AST >3×ULN; Total bilirubin >2×ULN; Creatinine clearance <30 mL/min.
- History of significant cardiovascular disease within 12 months prior to enrollment, including myocardial infarction, coronary intervention, unstable angina, or clinically significant arrhythmia.
- Other severe or uncontrolled medical conditions that may interfere with study participation or outcomes, including but not limited to uncontrolled diabetes, severe gastrointestinal disease, severe cardiopulmonary disease, autoimmune disease, immunodeficiency, or uncontrolled infections.
- History of severe immediate hypersensitivity reactions to study-related drugs, aminoglycosides, or biologic agents.
- Pregnant or breastfeeding women.
- Patients who are unable or unwilling to comply with study procedures or follow-up, or who have poor adherence as judged by the investigator.
- History of other malignancies unless disease-free for at least 3 years without active treatment (except for adequately treated non-melanoma skin cancer or carcinoma in situ).
- Receipt of live vaccines within 6 weeks prior to initiation of lymphodepleting chemotherapy.
- Major surgery within 14 days prior to enrollment or planned major surgery during the study period.
- Any other condition that, in the investigator's judgment, may increase risk, interfere with study results, or make the patient unsuitable for the study.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:CD22/CD19 Dual-Target CAR-T Cell Therapy
Patients will receive CD22/CD19 dual-target CAR-T cell therapy following lymphodepleting chemotherapy.
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Autologous CD22/CD19 dual-target chimeric antigen receptor T cells
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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1-year Event-Free Survival Rate (EFSR)
大体时间:1 years after CAR-T cell infusion
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The 1-year event-free survival rate after CD22/CD19 CAR-T cell therapy used as enhanced consolidation treatment in high-risk B-cell acute lymphoblastic leukemia.
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1 years after CAR-T cell infusion
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Overall Survival (OS)
大体时间:Up to 1 years after CAR-T cell infusion
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From the date of CAR-T cell infusion until the date of death or last follow-up, assessed up to 1 years.
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Up to 1 years after CAR-T cell infusion
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Time to Progression (TTP)
大体时间:Up to 1 years after CAR-T cell infusion
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Time to progression (TTP) is defined as the time from CD22/CD19 chimeric antigen receptor T-cell (CAR-T) cell infusion to the date of first documented disease progression, as assessed by standard response criteria.
Disease progression includes hematologic relapse, bone marrow relapse, or extramedullary disease progression.
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Up to 1 years after CAR-T cell infusion
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Disease-Free Survival (DFS)
大体时间:Up to 1 years after CAR-T cell infusion
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Disease-free survival (DFS) is defined as the time from CD22/CD19 chimeric antigen receptor T-cell (CAR-T) cell infusion to the first occurrence of disease relapse or death from any cause, whichever occurs first, in patients who achieve complete remission after treatment.
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Up to 1 years after CAR-T cell infusion
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Duration of Response (DOR)
大体时间:Up to 1 years after CAR-T cell infusion
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Duration of response (DOR) is defined as the time from the first documented achievement of complete remission or partial remission after CD22/CD19 chimeric antigen receptor T-cell (CAR-T) cell infusion to the date of disease relapse or progression, or death from any cause, whichever occurs first.
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Up to 1 years after CAR-T cell infusion
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Relapse Rate
大体时间:Up to 1 years after CAR-T cell infusion
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Relapse rate is defined as the proportion of patients who develop disease recurrence after achieving complete remission following CD22/CD19 CAR-T cell infusion, including hematologic, marrow, or extramedullary relapse.
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Up to 1 years after CAR-T cell infusion
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Incidence and Severity of Treatment-Emergent Adverse Events
大体时间:Up to 1 years after CAR-T cell infusion
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Include cytokine release syndrome (CRS), immune effector cell-associated neurotoxicity syndrome (ICANS), hematologic toxicities (anemia, leukopenia, neutropenia, thrombocytopenia), infections, electrolyte abnormalities, liver and renal function abnormalities, and other laboratory abnormalities.
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Up to 1 years after CAR-T cell infusion
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合作者和调查者
赞助
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- S2025-1062-02
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
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