Pilot Study Assessing the Feasibility of CD34+ Cells Mobilization and Collection After Treatment With G-CSF and Plerixafor in Patients With Fanconi Anemia for Subsequent Treatment by Gene Therapy
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 4
- 试验地点
- 1
- 主要终点
- level of CD34+ cells mobilization
研究概览
简要总结
The purpose of this study is to assess the feasibility of Plerixafor used in combination with G-CSF (Granulocyte Colony Stimulating Factor) in 5 Fanconi anemia patients to mobilize and collect a sufficient number of peripheral blood CD34+ cells for peripheral blood apheresis, for further gene therapy study.
详细描述
Fanconi anemia is an autosomal recessive disease with an average survival of around 24 years old. The number of cells producted by bone marrow decreases around 5-10 years old. Hematological symptoms occur around 7 years old. 80% of patients with Fanconi anemia have clinical signs of bone marrow failure in the first decade of life. Generally macrocytosis is the first noticeable sign. Then it leads to thrombocytopenia, anemia and pancytopenia.
Epidemiologic studies show that nearly all of the patients will have medullar aplasia before 40 years old, which is then the first cause of mortality.
It must be emphasized that these complications may occur simultaneously for the same patient, so joint therapeutic intervention is needed.
There is no basic treatment. Some currently used treatments cure cytopenias. These treatments involve blood transfusion, oral androgen, hematopoietic growth factor administration, such as Epo and G-CSF to treat anemia and neutropenia. These treatments are not curative. Hematopoietic stem cell transplantation is the only treatment able to restore permanently hematopoiesis. However, this treatment leads to a high level risk of developing solid tumors and other complications.
All these data justify of developing a stem cells gene therapy treatment using a lentiviral vector expressing wild-type FANCA gene under CIBER promoter.
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
- 2 Years 至 17 Years（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patient with Fanconi anemia
- •Patient from 2 to 17 years old
- •Potential indication for allogenic bone arrow graft without HLA-identical brotherhood available
- •Patient's weight >10kg
- •Treated and followed for at least the previous two years in a specialized center where they got a full assessment of their disease
- •For women of childbearing age, not pregnant and use of an effective contraception during the entire participation in the research.
- •Affiliated or beneficiary of an health insurance regimen
- •Informed and signed consent
排除标准
- •Patient unable to follow the visits required by the protocol
- •Positive serology for HIV-1/2, HTLV-1/2, HCV and HbS
- •Bacterial, viral, fungal or parasitic active infection with clinical signs
- •Personal history of cancer, myeloproliferative hematopathy or immune deficiency
- •Heart failure and / or heart rhythm disorder
- •History of allogeneic graft of hematopoietic stem cells
- •Patient with an HLA-identical brotherhood donor available
- •Myelodysplasia diagnose on myelogram
- •Cytogenetic abnormality on karyotype
- •Malignant solid tumor
- •Documented spontaneous genetic reversion of medullary process
- •Diagnosis of a psychiatric disorder that could compromise his/her ability to participate in the study
- •Any disorder according to the investigator, that could compromise the ability of patient to give his writing consent and/or to comply with requiring study's procedures
- •Current Pregnancy
- •Heart, kidney or liver failure
- •Current participation in another interventional clinical trial
- •Patient under Medical Assistance State
- •Hypersensitivity to plerixafor or any excipient contained in MOZOBIL®
- •Hypersensitivity to filgrastim or any of its' excipient
研究组 & 干预措施
Fanconi anemia
G-CSF and Plerixafor
干预措施: G-CSF (Drug)
Fanconi anemia
G-CSF and Plerixafor
干预措施: Plerixafor (Drug)
结局指标
主要结局
level of CD34+ cells mobilization
时间窗: from day 5 to day 8 after the first injection of G-CSF
次要结局
- number of treatment-related adverse events as a measure of tolerability(30 days after cytapheresis)