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临床试验/NCT01852370
NCT01852370Enrolling By Invitation1 期

Bilateral Orthotopic Lung Transplant in Tandem With CD3+ and CD19+ Cell Depleted Bone Marrow Transplant From Partially HLA-Matched Cadaveric Donors

Paul Szabolcs1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2013年6月20日最近更新:
干预措施
相关药物

试验速览

阶段
1 期
状态
Enrolling By Invitation
发起方
入组人数
16
试验地点
1
主要终点
Safety: Death

研究概览

简要总结

The purpose of this study is to determine whether bilateral orthotopic lung transplantation (BOLT) followed by cadaveric partially-matched hematopoietic stem cell transplantation (HSCT) is safe and effective for patients aged 5-45 years with primary immunodeficiency (PID) and end-stage lung disease.

详细描述

This is an original IND for an investigator initiated phase I/II study. The primary purpose of the study is to evaluate the safety and efficacy of performing bilateral orthotopic lung transplantation (BOLT) followed by cadaveric, partially HLA-matched CD3+/CD19+-depleted hematopoietic stem cell transplantation (HSCT) from the same donor for patients with primary immunodeficiency diseases (PID) and end-stage lung disease. For many patients with primary immunodeficiencies, HSCT is a curative, life-saving therapy, resulting in restoration of function in the immune system. Patients with primary immunodeficiencies often develop pulmonary complications as a result of chronic or recurrent infections, making them ineligible for HSCT due to the high risk of mortality and pulmonary complications. Lung transplant prior to HSCT would allow for restoration of pulmonary function prior to HSCT, allowing PID patients to proceed to HSCT, which would be curative for the patient's underlying immunodeficiency. As a secondary aim after successful engraftment with donor bone marrow, there is realistic hope for tolerating planned withdrawal of immunosuppression achieving eventual freedom from all immunosuppressive drugs and attaining a tolerant state.

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
5 Years 至 45 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

BOLT+BMT

Experimental

All patients will receive a double lung transplant followed by a hematopoietic stem cell transplant. The lungs and stem cells are from the same partially HLA-matched cadaveric donor. Prior to transplantation, the marrow will be negatively selected for CD3/CD19 using a CliniMACS® depletion device.

干预措施: CD3/CD19 negative allogeneic hematopoietic stem cells (Biological)

结局指标

主要结局

Safety: Death

时间窗: Up to 2 years post stem cell transplant

How many, if any, patients die.

Efficacy: T-cell chimerism

时间窗: 1 year post stem cell transplant

The number of patients who have ≥ 25% donor T-cell chimerism.

Safety: Rituximab

时间窗: Up to 2 years post stem cell transplant

The number of grade 4 and 5 events potentially related to rituximab.

Safety: Engraftment syndrome

时间窗: Up to 2 years post stem cell transplant

How many, if any, patients develop engraftment syndrome.

Efficacy: BOS score

时间窗: 1 year post stem cell transplant

Bronchiolitis Obliterans Syndrome (BOS) score for all patients who receive both lungs and stem cell transplants.

Safety: Engraftment failure

时间窗: Up to 2 years post stem cell transplant

How many patients, if any, develop engraftment failure.

Efficacy: Myeloid chimerism

时间窗: 1 year post stem cell transplant

The number of patients with myeloid disorders (e.g. CGD) who attain ≥ 10% myeloid chimerism.

Efficacy: B-cell chimerism

时间窗: 1 year post stem cell transplant

The number of patients with B-cell disorders who attain ≥ 10% B-cell chimerism.

次要结局

  • Graft failure(Up to 2 years post stem cell transplant)
  • Acute graft-versus-host disease (GVHD)(Up to 2 years post stem cell transplant)
  • Lymphocyte count - for T-cell lymphopenias(1 year post stem cell transplant)
  • Chronic graft-versus-host disease (GVHD)(Up to 2 years post stem cell transplant)
  • Ability to withdraw immunosuppression(1 year post stem cell transplant)
  • Allograft failure(1 year post lung transplant)
  • Tolerance(Up to 2 years post stem cell transplant)
  • Acute cellular rejection(Up to 2 years post stem cell transplant)
  • Time to withdraw immunosuppression(Up to 2 years post stem cell transplant)
  • Feasibility of meeting BMT eligibility critieria(Up to 2 years post stem cell transplant)
  • Long-term complications(Up to 2 years post stem cell transplant)
  • Pathogen-specific immunity(Up to 2 years post stem cell transplant)
  • Chronic lung allograft dysfunction(1 year post lung transplant)
  • Rituximab related adverse events(From the time of the first dose of rituximab up to the start of BMT conditioning.)

研究者

发起方
Paul Szabolcs
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Paul Szabolcs

Chief, Division of Blood and Marrow Transplant, Children's Hospital of Pittsburgh of UPMC

University of Pittsburgh

研究点 (1)

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