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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

2026年6月23日 更新者:Liping Dou

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

This single-center, open-label, single-arm, prospective study will evaluate the safety, tolerability, and efficacy of CD22/CD19 dual-target chimeric antigen receptor T-cell (CAR-T) therapy as consolidation treatment in patients with high-risk B-cell acute lymphoblastic leukemia (B-ALL) who have achieved first remission after standard induction therapy and consolidation chemotherapy. Approximately 30 patients will be enrolled. Participants will undergo screening, cell collection for CAR-T manufacturing, lymphodepleting chemotherapy, and subsequent CAR-T cell infusion, followed by scheduled safety and efficacy follow-up. Safety assessments will include monitoring for cytokine release syndrome (CRS), neurotoxicity, hematologic toxicity, organ toxicity, infections, and other adverse events. Efficacy assessments will include event-free survival (EFS), overall survival (OS), progression-free survival (PFS), duration of response(DOR), relapse, and mortality. Exploratory analyses will assess CAR-T cell kinetic characteristics and clonal evolution after treatment.

研究概览

研究类型

介入性

注册 (估计的)

30

阶段

  • 阶段2
  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Beijing Municipality
      • Beijing、Beijing Municipality、中国、100853
        • 招聘中
        • Chinese PLA General Hospital

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. 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.
  2. 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).
  3. 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.

  4. Age between 18 and 85 years, regardless of sex.
  5. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
  6. Estimated life expectancy ≥3 months.
  7. Hemoglobin ≥60 g/L (transfusion allowed).
  8. Absolute neutrophil count ≥1,000/μL and platelet count ≥45,000/μL.
  9. 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.

  10. 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:

  1. 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.

  2. Prior treatment with any CAR-T cell therapy or other genetically modified T-cell therapies.
  3. 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.)

  4. Non-disease-related hepatic or renal dysfunction defined as:

    ALT or AST >3×ULN; Total bilirubin >2×ULN; Creatinine clearance <30 mL/min.

  5. History of significant cardiovascular disease within 12 months prior to enrollment, including myocardial infarction, coronary intervention, unstable angina, or clinically significant arrhythmia.
  6. 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.
  7. History of severe immediate hypersensitivity reactions to study-related drugs, aminoglycosides, or biologic agents.
  8. Pregnant or breastfeeding women.
  9. Patients who are unable or unwilling to comply with study procedures or follow-up, or who have poor adherence as judged by the investigator.
  10. 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).
  11. Receipt of live vaccines within 6 weeks prior to initiation of lymphodepleting chemotherapy.
  12. Major surgery within 14 days prior to enrollment or planned major surgery during the study period.
  13. 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

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

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
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.
Autologous CD22/CD19 dual-target chimeric antigen receptor T cells

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
1-year Event-Free Survival Rate (EFSR)
大体时间:1 years after CAR-T cell infusion
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.
1 years after CAR-T cell infusion

次要结果测量

结果测量
措施说明
大体时间
Overall Survival (OS)
大体时间:Up to 1 years after CAR-T cell infusion
From the date of CAR-T cell infusion until the date of death or last follow-up, assessed up to 1 years.
Up to 1 years after CAR-T cell infusion
Time to Progression (TTP)
大体时间:Up to 1 years after CAR-T cell infusion
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.
Up to 1 years after CAR-T cell infusion
Disease-Free Survival (DFS)
大体时间:Up to 1 years after CAR-T cell infusion
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.
Up to 1 years after CAR-T cell infusion
Duration of Response (DOR)
大体时间:Up to 1 years after CAR-T cell infusion
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.
Up to 1 years after CAR-T cell infusion
Relapse Rate
大体时间:Up to 1 years after CAR-T cell infusion
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.
Up to 1 years after CAR-T cell infusion
Incidence and Severity of Treatment-Emergent Adverse Events
大体时间:Up to 1 years after CAR-T cell infusion
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.
Up to 1 years after CAR-T cell infusion

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年1月1日

初级完成 (估计的)

2026年12月31日

研究完成 (估计的)

2027年12月31日

研究注册日期

首次提交

2026年5月4日

首先提交符合 QC 标准的

2026年5月4日

首次发布 (实际的)

2026年5月8日

研究记录更新

最后更新发布 (实际的)

2026年6月25日

上次提交的符合 QC 标准的更新

2026年6月23日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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