Phase I Study of Anti-Human CD45 Monoclonal Antibodies in Patients With Advanced Leukemia Prior to Allogeneic Stem Cell Transplantation (ADVL)
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 6
- 试验地点
- 2
- 主要终点
- To evaluate the toxicity and the anti-tumor activity of anti-human CD45 antibodies (anti-CD45) administered to patients with relapsed/resistant leukemia prior to bone marrow transplantation.
研究概览
简要总结
Participants in this study have a hematologic malignancy which is a disorder in the bone marrow that affects the body's ability to create blood. Participants might benefit from receiving an allogeneic stem cell transplant (meaning the cells come from a donor). The participants donor is a family member. Stem cells are cells in the bone marrow and blood that can form a whole new blood system.
详细描述
Patients are given high doses of chemotherapy before receiving a stem cell transplant to keep their immune system from rejecting the donor stem cells and to kill any diseased cells that remain in the body. To try and improve on the results of transplants that use high dose chemotherapy alone, we are adding an agent called anti-CD45 to the treatment prior to the stem cell transplant. Anti-CD45 is an antibody that specifically finds and destroys leukemia cells.
Patients will receive the anti-CD45 with high dose chemotherapy (including Ara-C and Cyclophosphamide) and radiotherapy. Patients will also receive Mesna which is a drug that helps prevent bladder damage which can be caused by the cyclophosphamide. High dose radiotherapy is also known as Total Body Irradiation or TBI.
Patients will receive the anti-CD45, high dose chemotherapy, and high dose radiotherapy before the stem cell transplant. We expect participation in this study will last 2 years.
A summary of the treatment follows:
- Day - 7: Ara-C, Cyclophosphamide, Mesna
- Day - 6: Ara-C, Cyclophosphamide, Mesna
- Day - 5: Ara-C, Anti-CD45
- Day - 4: Anti-CD45, TBI
- Day - 3: Anti-CD45, TBI
- Day - 2: Anti-CD45, TBI
- Day - 1: TBI
- Day 0: Stem Cell Infusion (transplant)
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
- — 至 45 Years（Child, Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with advanced leukemia or other hematologic malignancy including AML, ALL, CML, and MDS. Advanced features include: a) Induction failure, prolonged induction beyond 6 weeks b) Incomplete response to salvage therapy c) CML in blast crisis or acute leukemia in chemotherapy resistant relapse d) secondary leukemia or secondary myelodysplastic disease
- •Patients must have a suitable HLA identical sibling donor or 5/6 matched related donor, or fully matched or 5/6 matched unrelated donor, or haploidentical related donor.
排除标准
- •Patients with a life expectancy (2X normal for age)
- •Patients with known allergy to rat serum products
- •Patients with a Lansky score <60% or Karnofsky score <60%.
- •Patients with severe infection that on evaluation by the PI precludes ablative radio/chemotherapy or successful transplantation.
- •Patients with sever personality disorder or mental illness.
- •Patients with documented HIV positivity
- •Pregnant or lactating females
研究组 & 干预措施
1
干预措施: CAMPATH-1H (Drug)
1
干预措施: Anti-CD45 (Drug)
1
干预措施: Ara-C (Drug)
1
干预措施: Cyclophosphamide (Drug)
1
干预措施: Mesna (Drug)
1
干预措施: Total Body Irradiation (Radiation)
结局指标
主要结局
To evaluate the toxicity and the anti-tumor activity of anti-human CD45 antibodies (anti-CD45) administered to patients with relapsed/resistant leukemia prior to bone marrow transplantation.
时间窗: 28 days and 100 days post transplant
次要结局
- To describe the effects of anti-CD45 on normal hematopoiesis and on complement levels and to describe the effects of anti-CD45 on leukemic blast cells.(100 days post transplant)
研究者
Robert Krance
Professor, Pediatrics-Hem-Onc Cell & Gene
Baylor College of Medicine