来自相关或无关供体的 Alpha/Beta T 细胞耗尽造血干细胞移植治疗儿童和青年血液病
TCRαβ+ 和 CD19+ 耗尽的造血干细胞移植,来自密切匹配的无关供体或单倍体相关供体,用于治疗儿童和年轻人的血液病
This study is being done to see if the investigators can take peripheral blood stem cells from either an adult family member or a closely matched unrelated donor, and run them through a special lab instrument to remove alpha/beta T cells and B cells and then give them to the patient to treat disease. This is an experimental way of doing a hematopoietic stem cell transplant (HSCT). The investigators want to see if the new stem cells will grow without bad graft vs. host disease (GVHD). This treatment approach is experimental in the United States.
研究概览
地位
条件
详细说明
This single institution, phase I clinical trial will determine the safety and feasibility of employing T-cell receptor (TCR) αβ+ and CD19+ (Cluster of Differentiation) depleted hematopoietic stem cell transplantation (HSCT) using peripheral blood stem cells (PBMC) from closely matched unrelated donors or haploidentical donors to treat non-malignant hematologic diseases in children and young adults. Allogeneic hematopoietic stem cell transplantation has become a curative option for children and adolescents with a variety of otherwise fatal conditions. To reduce the incidence and severity of graft-versus-host disease (GVHD) associated with allogeneic hematopoietic stem cell transplantation, donor grafts are depleted of T cells, either using CD34+ selection or CD3+/CD19+ depletion of grafts. However, these selection processes also deplete the graft of protective cell subsets, such as γδ T cells, natural killer (NK) cells, monocytes and dendritic cells, which play important roles in the immune response to infectious agents. Moreover, the presence of NK cells and γδ T cells in donor grafts is associated with more rapid immune reconstitution after HSCT transplantation. In order to retain these protective immune cell subsets, this trial will use a novel, highly selective graft engineering process using the Miltenyi CliniMACS system that selectively depletes αβ-T cells and B cells that are responsible for GVHD and Epstein Barr Virus (EBV)-related post-transplantation lymphoproliferative disorder, respectively. Prior to transplantation, patients will be treated with a conditioning regimen, specific for the original disorder.
The primary objective of this study is evaluation of the safety and feasibility of HSCT using TCRαβ+/CD19+ depleted hematopoietic stem cells to treat non-malignant hematologic diseases. This will be assessed by evaluating the incidence of graft failure, grade III-IV acute GVHD and chronic GVHD and TRM.
Secondary objectives include the evaluation of immune reconstitution and incidence of post-transplant infections, adverse events, serious adverse events, overall and disease-free survival and the efficiency of graft processing by the CliniMACS System.
研究类型
注册 (估计的)
阶段
- 阶段1
联系人和位置
学习联系方式
- 姓名:Celeste Matsushima
- 电话号码:608-890-8069
研究联系人备份
- 姓名:Jenny Weiland
- 电话号码:608-890-8070
- 邮箱:PedsHemOncResearch@lists.wisc.edu
学习地点
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Wisconsin
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Madison、Wisconsin、美国、53792
- 招聘中
- American Family Children's Hospital
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
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No Human leukocyte antigen (HLA) identical sibling available AND
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NO HLA matched unrelated donor available OR urgent need of HSCT precludes time necessary to search for suitable HLA matched unrelated donor AND
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Haploidentical donor OR closely matched unrelated donor available and willing to undergo mobilization and apheresis
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If subject has genetically confirmed inherited bone marrow failure, related donor must be evaluated for this disorder and testing must be negative.
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If subject has sickle cell disease, donor must be unaffected or have only sickle cell trait
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Patient must be diagnosed with one of the following diseases or disorders:
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Hemoglobinopathies
- Sickle Cell Disease for patients ≤ 21 years of age for whom hydroxyurea has been trialed for at least six months, and failed
- Thalassemia Major for patients ≤ 21 years of age
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Acquired Bone Marrow Failure Syndromes
- Paroxysmal Nocturnal Hemoglobinuria with bone marrow failure
- Myelodysplastic Syndromes (lower risk)
- Severe acquired aplastic anemia
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Inherited Bone Marrow Failure Syndromes
- Fanconi Anemia
- Diamond Blackfan Anemia
- Dyskeratosis Congenita and related telomere disorders
- Congenital Thrombocytopenia Syndromes
- Severe Congenital Neutropenia
- Shwachman-Diamond Syndrome
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Inborn Errors of Immunity (IEI) or Primary Immune Regulatory Disorders (PIRD)
- Wiskott-Aldrich syndrome (WAS)
- Chronic granulomatous disease (CGD)
- Severe combined immunodeficiency (SCID)
- Primary hemophagocytic lymphohistiocytosis (HLH)
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Age ≤ 25 years (except patients with hemoglobinopathies)
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Life Expectancy ≥ 3 months
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Karnofsky (patients > 16 years)/Lansky (patients ≤ 16 years) index ≥ 60
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Organ Function Requirements
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Renal Function
- Creatinine clearance or radioisotope Glomerular Filtration Rate (GFR) greater than or equal to 60 ml/min/1.73m^2
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Liver Function
- Total bilirubin < 3 mg/dL
- Alanine aminotransferase (ALT)/ Serum glutamic-pyruvic transaminase; synonymous with ALT (SCPT) ≤ 3 x Upper Limit of Normal (ULN) for age
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Cardiac Function
- Ejection fraction of > 40% by Multiple gated acquisition scan (MUGA) or echocardiogram
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Pulmonary Function
- No evidence of dyspnea at rest
- No supplemental oxygen requirement
- If measured, carbon monoxide diffusion capacity (DLCO) > 50%
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Willing to use effective birth control method if patient is of reproductive potential
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Informed consent obtained (patient or legal representative)
Exclusion Criteria:
- Pregnant
- HIV infection
- Uncontrolled, serious active infection at screening
- Significant serious intercurrent illnesses
- Enrollment in any other treatment study that would interfere with the endpoints of this study according to judgement of Principal Investigator (or PI designee).
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:Treatment arm
Participants will undergo a conditioning regimen, specific for the original disease, After that peripheral blood stem cell transplant from a haploidentical donor or closely matched unrelated donor, depleted of TCRαβ+ and CD19+ cells using the CliniMACS TCR α/β-biotin and CD19 Systems will be administered intravenously on Day 0 to all participants. |
After undergoing a disease specific conditioning regimen (standard of care), participants will receive peripheral blood stem cell transplant from a haploidentical donor or closely matched unrelated donor, depleted of TCR αβ+ and CD19+ cells using the CliniMACS TCR α/β-biotin and CD19 Systems. The CliniMACS Cell Selection System is based on magnetic-activated cell sorting mechanism. The CliniMACS device is a powerful tool for the isolation of many cell types from heterogeneous cell mixtures. |
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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Incidence of grade III-IV acute graft-versus-host disease (GVHD)
大体时间:100 days post transplantation
|
Acute GVHD will be assessed and graded according to the Keystone Consensus Criteria for staging and grading of acute graft-versus-host disease. |
100 days post transplantation
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Incidence of extensive chronic GVHD
大体时间:up to 2 years
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Chronic GVHD will be assessed according to the current CIBMTR (Center for International Blood and Marrow Transplant Research) manual reflecting a grading system published by Sullivan KM (Sullivan 1981). |
up to 2 years
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Incidence of graft failure
大体时间:up to 2 years after graft
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Graft failure - defined as failure to achieve ANC > 500 /µL at Day +28 or initial neutrophil engraftment followed by a decline in ANC < 500 /µL that is unresponsive to growth factor therapy (secondary graft failure). |
up to 2 years after graft
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Incidence of Treatment Related Mortality (TRM)
大体时间:Day +100 post-HSCT
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TRM - defined as death from any cause other than disease progression. |
Day +100 post-HSCT
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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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总生存期(OS)
大体时间:长达 2 年
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长达 2 年
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CliniMACS 系统效率:TCRαβ+ 和 CD19+ 耗尽程序后恢复的活 CD34+ 细胞百分比
大体时间:HSCT 后长达 12 个月
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HSCT 后长达 12 个月
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GVHD 发病率与供体杀伤细胞免疫球蛋白样受体 (KIR) 单倍型含量的相关性
大体时间:长达 2 年
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长达 2 年
|
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GVHD 发病率与供体和受体之间的杀伤细胞免疫球蛋白样受体 (KIR)/KIR 配体错配之间的相关性。
大体时间:长达 2 年
|
长达 2 年
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发生与输注 HSC 移植物相关的不良事件的参与者人数
大体时间:第 0 天
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第 0 天
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严重不良事件的发生率
大体时间:长达 2 年
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长达 2 年
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CliniMACS system efficiency: log depletion value for CD19/CD20+ B cells after the TCRαβ+ and CD19+ depletion procedure
大体时间:Day 0
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Day 0
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CliniMACS system efficiency: log depletion value of TCRαβ+ T cells after the TCRαβ+ and CD19+ depletion procedure
大体时间:Day 0
|
Day 0
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Time to neutrophil engraftment
大体时间:up to 28 days following HSCT
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The time to neutrophil engraftment is defined as the post-transplant day that is the first of 3 consecutive days with an absolute neutrophil count (ANC) of >500/µL as assessed by CBC. |
up to 28 days following HSCT
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Time to platelet engraftment
大体时间:up to 28 days following HSCT
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The time to platelet engraftment is defined as the post-transplant day that is the first of 3 consecutive days with a platelet count ≥ 20,000/µL as assessed by complete blood count (CBC), without platelet support (transfusion) for 7 days. |
up to 28 days following HSCT
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Percentage donor chimerism using Short Tandem Repeat (STR)
大体时间:up to 12 months following HSCT
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Short tandem repeat (STR) analysis will provide the percentage donor chimerism at specific time points post-transplant. |
up to 12 months following HSCT
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Kinetics of lymphocyte reconstitution via immunophenotyping using flow cytometry
大体时间:up to 12 months following HSCT
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Lymphocyte reconstitution will be assessed at specific time points post-HSCT, expressed as the percentage of white blood cells comprised of T, B and NK cell subsets. |
up to 12 months following HSCT
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CliniMACS system efficiency: number of viable blood cell subsets after the TCRαβ+ and CD19+ depletion procedure
大体时间:Day 0
|
Number of viable CD34+ blood stem cells, CD20+ B cells, CD3-CD56+ NK cells, TCRαβ+ T cells, and TCRγδ+ T cells in the HSC graft after the TCRαβ+ and CD19+ depletion procedure |
Day 0
|
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Event free survival
大体时间:up to 1 years
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An event is defined as death, graft failure or stable mixed chimerism with disease recurrence. |
up to 1 years
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Incidence of symptomatic bacterial/fungal and viral reactivation requiring therapy
大体时间:up to 1 year
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The incidence of infections (symptomatic bacterial/fungal and viral reactivation requiring therapy) will be used as an additional safety measure |
up to 1 year
|
合作者和调查者
调查人员
- 首席研究员:Christian Capitini, MD、University of Wisconsin, Madison
- 研究主任:Jacques Galipeau, MD、University of Wisconsin, Madison
研究记录日期
研究主要日期
学习开始 (估计的)
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
其他研究编号
- 2020-1251
- A536755 (其他标识符:UW Madison)
- UW19113 (其他标识符:OnCore ID)
- 2020-1251 (其他标识符:HS IRB UW Madison)
- NCI-2021-02128 (注册表标识符:NCI CTRP)
- Protocol Version 6 (其他标识符:HS-IRB UW Madison)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
The Principal Investigator, Sponsor and funding institutions (if applicable) will ensure that all mechanisms used to share data include proper plans and safeguards to protect the rights and privacy of participants who participate in this research.
IPD 共享支持信息类型
- 研究方案
- 树液
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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