Partial Stem Cell Transplant for Sickle Cell Disease From Matched Donors
Matched Related Donor Non-myeloablative Hematopoietic Cell Transplantation With Alemtuzumab, 400 cGy TBI, and Abatacept for Sickle Cell Disease and Beta-Thalassemia
研究概览
地位
详细说明
Study Description:
Our prior non-myeloablative conditioning regimen (03H0170) included 1mg/kg of alemtuzumab divided over 5 days, 300 cGy total body irradiation (TBI), and sirolimus for immune suppression. Sickle disease-free survival (DFS) and overall survival (OS) were 85% and 94% respectively, graft failure 15%, no transplant related mortality (TRM), and acute or chronic GVHD <5%. A large proportion of patients achieved robust (>=95%) donor myeloid chimerism at day 30, but this proportion decreased quickly to 67.2% at 1, 64.9% at 2, and 60% at 3, and 56.9% at 4 years post-transplant.
A subsequent protocol (000539H) added briquilimab, an antibody targeting CD117 (c-Kit), to alem-300 cGy TBI regimen, but did not reduce the gradual decline in donor myeloid chimerism as originally hypothesized, leading to protocol closure. Rates of graft failure was 20%, no TRM, acute GVHD was 5%, and no chronic GVHD. We now propose to increase TBI to 400 cGy to further deplete host lymphoid and myeloid cells to achieve a higher percentage of donor leukocyte engraftment without substantially increasing toxicity. Since we will continue to use filgrastim to mobilize and collect donor hematopoietic cells, we also add abatacept to preserve the low rates of GVHD.
Objectives:
Primary Objective:
To reduce the proportion of patients with graft failure or donor myeloid chimerism <95%
Secondary Objectives:
- To compare CD14/15 and CD3 chimerism to prior MRD HCT protocols (03-H-0170, 14-H-0077, and 000539H)
- To assess the usual transplant related parameters, such as count recovery, transfusion support, rates of GVHD, viral/bacterial infections, rates of transplant related and overall mortality, and compare to prior MRD HCT protocols
Tertiary Objectives:
- To compare changes in organ function
- To examine neuropsychological functioning, wellbeing, and pain before and after HCT
- To obtain reproductive health related changes before and after HCT
Endpoints:
Primary Endpoint: proportion of participants with graft failure or myeloid chimerism <95% at 1 year post HCT
Secondary Endpoints:
- Percent myeloid (CD14/15) chimerism at day 30, 60, 100, 1 year, 2 years, and 3 years post HCT
- Percent T cell (CD3) chimerism at day 30, 60, 100, 1 year, 2 years, and 3 years post HCT
- Day of neutrophil engraftment per CIBMTR definition
- Day of platelet engraftment per CIBMTR definition
- Rates of viral reactivation or infection to day 100 post HCT
- Rates of acute and chronic GVHD at 1 and 2 years post HCT, respectively
- Rates of graft failure or myeloid chimerism <95% at 1 year post HCT
- Transplant related mortality at 1, 2, and 3 years post HCT
- Non-transplant related mortality at 1, 2 and 3 years post HCT
Exploratory Endpoints:
-Quality of life, neuropsychologic function, reproductive health questionnaires, serial testing or imaging of organ function/status
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:John F Tisdale, M.D.
- 电话号码:(301) 402-6497
- 邮箱:johntis@mail.nih.gov
研究联系人备份
- 姓名:Kelly S Norris, R.N.
- 电话号码:(301) 529-7104
- 邮箱:kelly.norris@nih.gov
学习地点
-
-
Maryland
-
Bethesda、Maryland、美国、20892
- 招聘中
- National Institutes of Health Clinical Center
-
接触:
- NIH Clinical Center Office of Patient Recruitment (OPR)
- 电话号码:TTY dial 711 800-411-1222
- 邮箱:ccopr@nih.gov
-
-
参与标准
资格标准
适合学习的年龄
- 孩子
- 成人
- 年长者
接受健康志愿者
描述
- INCLUSION CRITERIA
RECIPIENT:
Participants must fulfill one disease category (1 or 2) and 3
Patients with sickle cell disease at high risk for disease related morbidity or mortality, defined by having an end-organ damage (A, B, C, D, OR E) or complication(s) not ameliorated by sickle cell-specific therapies (F):
A. Stroke defined as a clinically significant neurologic event that is accompanied by an infarct on cerebral MRI ORb
B. Abnormal trans-cranial Doppler examination (>=200 cm/s); OR
C. Silent cerebral infarct defined as an infarct-like lesion based on an MRI signal abnormality at least 3 mm in one dimension and visible in two planes on FLAIR or T2- weighted images (or similar image with 3D imaging) and documented neurological examination performed by a neurologist demonstrating the participant has a normal neurologic examination, or an abnormality on examination that could not be explained by the location of the brain lesion(s); OR
D. Sickle cell related renal insufficiency defined by a creatinine level >=1.5 times the upper limit of normal and kidney biopsy consistent with sickle cell nephropathy OR nephrotic syndrome OR creatinine clearance <60mL/min/1.73m2 for patients <16 years of age or <50mL/min for patients >16 years of age OR requiring peritoneal or hemodialysis; OR
Age (Years): <= 5 / Upper limit of normal serum creatinine (mg/dl): 0.8
Age (Years): 5 < age <= 10 / Upper limit of normal serum creatinine (mg/dl): 1.0
Age (Years): 10 < age <= 15 / Upper limit of normal serum creatinine (mg/dl): 1.2
Age (Years): > 15 / Upper limit of normal serum creatinine (mg/dl): 1.3
E. Tricuspid regurgitant jet velocity (TRV) of >=2.5 m/s in patients at least 3 weeks after a vaso-occlusive crisis; OR
F. Recurrent severe priapism defined as at least two episodes of an erection lasting >=4 hours requiring medical intervention (e.g. aspiration, injection of vasoconstrictor, prior penile surgery.); OR
G. Sickle hepatopathy defined as EITHER ferritin >1000mcg/L OR direct bilirubin >0.4 mg/dL at baseline; OR
H. Vaso-occlusive crises: more than 1 hospital admission per year while on a therapeutic dose of sickle cell treatment /medication; OR
I. Acute chest syndrome (ACS): any ACS while on sickle cell treatment /medication
Patients with beta-thalassemia who have grade 2 or 3 iron overload, determined by the presence of 2 or more of the following:
- Portal fibrosis by liver biopsy
- Inadequate chelation history (defined as failure to maintain adequate compliance with chelation with deferoxamine initiated within 18 months of the first transfusion and administered at least 5 days each week)
- Hepatomegaly of greater than 2 cm below the costochondral margin or by other imaging scans
Non disease specific
- Ages >=4 years and less than 65 years old
- Fully matched human leukocyte antigen (HLA) donors at A, B, C, and DR loci (8 of 8 or 10 of 10)
- Ability to comprehend and willing to sign an informed consent, assent obtained from minors when applicable. Negative serum or urine beta-HCG, when applicable
Agree to use birth control throughout the study and 3 months after abatacept or sirolimus administration.
- Female subjects must agree to use a medically acceptable method of birth control such as oral contraceptive, intrauterine device, barrier and spermicide, or implant/injection from start of screening until immunosuppression is stopped.
- Male subjects must agree to use effective contraception (including condoms) from start of screening until immunosuppression is stopped.
DONOR:
- Fully matched human leukocyte antigen (HLA) donors at A, B, C, and DR loci (8 of 8 or 10 of 10) are intended for this study.
- Donors age 4 or older and >=15 kg (or weight deemed acceptable by IR for line placement, DTM for apheresis, and pediatric consult service) eligible to donate hematopoietic stem cells, are eligible for this study.
- Donors will be evaluated in accordance with existing Standard NIH Policies and Procedures for determination of eligibility and suitability for clinical donation. Donors will sign on a separate protocol, 20-H-0099 NHLBI standard of care protocol for the mobilization and collection of HSCs. Note that participation in this study is offered to all eligible donors, but is not required for a donor to make a stem cell donation, so it is possible that not all donors will enroll onto this study.
EXCLUSION CRITERIA
RECIPIENT:
- Karnofsky or Lanksy performance status of <40
- Diffusing capacity of carbon monoxide <35% predicted: DLCO corrected for hemoglobin or KCO (corrected for lung volume). This criterion may be omitted in young children (e.g. near age 5) or other individuals who may have difficulty understanding or complying with instructions of testing.
- Baseline oxygen saturation of <85% or PaO2 <70
- Left ventricular ejection fraction: <35% estimated by ECHO
- Transaminases >5x upper limit of normal for age
- Evidence of uncontrolled bacterial, viral, or fungal infections (currently taking medication and progression of clinical symptoms) within one month prior to starting the conditioning regimen
- Major anticipated illness or organ failure incompatible with survival from HCT
- Pregnant or breastfeeding
DONOR:
- Pregnant or breastfeeding
- Cognitively impaired subjects
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:非随机化
- 介入模型:顺序分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
其他:Matched related donors
Donors for patients
|
About 5 tablespoons of blood will be collected from donors for research purposes.
|
|
实验性的:Transplant recipients
Patients with symptomatic sickle cell disease or beta-thalassemia
|
About 5 tablespoons of blood will be collected from donors for research purposes.
Total Body Irradiation 400 cGy
1 mg/kg
10 mg/kg x 6
|
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 |
|---|---|---|
|
Donor myeloid chimerism
大体时间:1 year
|
percentage of donor myeloid chimerism
|
1 year
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Donor CD3 chimerism
大体时间:1 year
|
percentage of donor myeloid chimerism
|
1 year
|
|
Overall survival
大体时间:1 year
|
percentage of patients surviving at 1 year
|
1 year
|
|
Acute Graft versus Host Disease
大体时间:1 year
|
percentage of patients with Grade 2-4 acute GVHD
|
1 year
|
合作者和调查者
调查人员
- 首席研究员:John F Tisdale, M.D.、National Heart, Lung, and Blood Institute (NHLBI)
出版物和有用的链接
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
- 10002545
- 002545-H
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
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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