Renal Allograft Tolerance Through Mixed Chimerism
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 5
- 试验地点
- 1
- 主要终点
- Number of Participants Successfully Withdrawn Off of Immunosuppressant Medication for 104 Weeks
研究概览
简要总结
In small initial studies, combined kidney and bone marrow transplants from the same donor have permitted some individuals to stop taking anti-rejection medicines without rejecting their transplant. This clinical trial will study this method in a greater number of people to determine if it is indeed effective and safe.
详细描述
All patients receiving an organ or tissue transplant must take special medicines known as "immunosuppressive drugs" in order to prevent the immune system from rejecting the transplant. These drugs can be very effective, but they leave the patient at an increased risk of serious infections and certain types of cancer. New methods of preventing transplant rejection are needed.
Researchers have found that transplanting both bone marrow and a kidney from the same donor can create what is called "mixed chimerism." This means that the transplant recipient has a mixture of the donor and recipient's immune systems. It is believed that this mixture of immune cells can prevent rejection of the kidney. In a small prior study, performing a kidney transplant together with a bone marrow transplant from the same donor allowed 4 of 5 patients to stop taking immunosuppressive drugs altogether, without rejecting their transplant. This clinical trial will study more patients to confirm if the technique is safe and effective.
Patients eligible for this study must be candidates for a living kidney transplant, and have an eligible donor identified. The transplant recipient and donor must both consent to participate in this study. Transplant recipients enrolled in the study will receive both kidney and bone marrow transplants from the same living donor. Prior to the transplant procedure, the transplant recipient will undergo a "conditioning regimen" that prepares their immune system for the recipient's immune (bone marrow) cells. This conditioning regimen is a combination of chemotherapy, radiation, immunosuppressive drugs and specialized medications called rituximab and MEDI-507. MEDI-507 is an investigational medication that has not been approved by the FDA. After the transplant procedure, transplant recipients will be prescribed steroids for several weeks and immunosuppressive drugs. After 2 months, the dose of the immunosuppressive drugs will slowly be decreased to zero in patients whose immune system and kidney function meet certain criteria.
Transplant recipients enrolled into the study will be hospitalized for 1 week prior to the transplant procedure. After the transplant, patients will remain in the hospital until the doctor feels they are well enough to go home. Recipients will receive approximately monthly checkups over a period of 2 years after transplant, plus a checkup at 2 ½, 3, 3 ½ , 4, and 5 years after transplant. Checkups will include physical exams, and blood and urine tests to assess immune system and kidney function. At four of these checkups, a kidney biopsy will be requested.
Transplant donors enrolled in the study will attend a screening visit, which will include a physical exam, blood tests and chest x-ray. Eligible donors will be admitted to the hospital for 3-5 days, where bone marrow will be collected prior to removal of the kidney. Transplant donors may be asked at a later date to donate additional blood samples for research purposes.
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
- 18 Years 至 60 Years(Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Awaiting first or second transplant with a living donor or first transplant with a cadaveric donor
- •For living-donor transplants, must have one or more HLA antigen-mismatched donors identified
- •Serologic evidence of prior exposure to Epstein-Barr virus (EBV)
排除标准
- •ABO blood group-incompatibility for a kidney graft of tissue from a donor
- •Decreased circulating white blood cell count
- •Positive for HIV-1, hepatitis B and C viruses
- •Have had prior radiation therapy that could limit dose
- •Lung capacity <50% of predicted normal
- •Evidence of insufficient cardiac capacity
- •Unwilling to use adequate contraception until 2 years after transplant
- •Lactation or pregnancy
- •Presence of antibody against the donor
研究组 & 干预措施
Kidney and Marrow Recipients
Combined kidney and bone marrow transplant
干预措施: Kidney Transplantation (Procedure)
Kidney and Marrow Recipients
Combined kidney and bone marrow transplant
干预措施: Bone marrow transplantation (Procedure)
Kidney and Marrow Recipients
Combined kidney and bone marrow transplant
干预措施: MEDI-507 (Biological)
Kidney and Marrow Recipients
Combined kidney and bone marrow transplant
干预措施: corticosteroids (Drug)
Kidney and Marrow Recipients
Combined kidney and bone marrow transplant
干预措施: cyclophosphamide (Drug)
Kidney and Marrow Recipients
Combined kidney and bone marrow transplant
干预措施: rituximab (Biological)
Kidney and Marrow Recipients
Combined kidney and bone marrow transplant
干预措施: Tacrolimus (Drug)
Kidney and Marrow Recipients
Combined kidney and bone marrow transplant
干预措施: thymic irradiation (Radiation)
结局指标
主要结局
Number of Participants Successfully Withdrawn Off of Immunosuppressant Medication for 104 Weeks
时间窗: 48 months post-transplant
A participant was considered a success if they were off immunosuppressive therapy for 104 consecutive weeks leading up to study week 208 (48 months post-transplant) or study termination, whichever occurred first.
次要结局
- Percentage of Participants Experiencing Acute Rejection(Transplantation until study completion or participant termination (up to five years))
- Change in Renal Function(Transplantation until study completion or participant termination (up to five years))
- Percentage of Participants With Graft Survival Through 156 Weeks(Transplantation until week 156)
- Percentage of Participants Surviving Through 156 Weeks(Transplantation until week 156)
- Time to Neutrophil Recovery Following Transplant(Transplantation until study completion or participant termination (participants followed up to five years))
- Time to Platelet Recovery Following Transplant(Transplantation until study completion or participant termination (participants followed up to five years))
- Percentage of Participants Experiencing a Clinically Significant Invasive or Resistant Opportunistic Infection(Transplantation until study completion or participant termination (participants followed up to five years))
