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临床试验/NCT00033475
NCT00033475已完成3 期

Cytotoxic T Cell Therapy for Post Transplant Lymphoproliferative Disease: Randomized Controlled Trial in Transplant Recipients

University of Edinburgh12 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2001年3月1日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
50
试验地点
12
主要终点
Complete response

研究概览

简要总结

RATIONALE: Some types of lymphoproliferative disease are associated with Epstein-Barr virus. Combining reduced immunosuppressive therapy with donor white blood cells that have been treated in the laboratory to kill cells infected with Epstein-Barr virus may be an effective treatment for lymphoproliferative disease.

PURPOSE: Randomized phase III trial to compare the effectiveness of reducing immunosuppressive therapy with or without donor white blood cells in treating patients who have Epstein-Barr virus-associated lymphoproliferative disease after organ transplantation.

详细描述

OBJECTIVES:

  • Determine the efficacy of treatment with partially HLA-matched allogeneic cytotoxic T cells and reduction of immunosuppression, in terms of survival rate and time to remission in patients with Epstein-Barr virus-associated B-cell lymphoproliferative disease after solid organ transplantation.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to transplanted organ type and transplant center. Patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients undergo sliding-scale reduction of immunosuppressive drugs from 1 of 5 regimens at physician's discretion. Patients then receive partially HLA-matched allogeneic cytotoxic T cells IV over 5 minutes once weekly for a total of 4 weeks.
  • Arm II: Patients undergo reduction of immunosuppression as in arm I alone. Patients are followed monthly for 6 months and then every 3 months for 2 years.

PROJECTED ACCRUAL: A total of 50 patients will be accrued for this study.

研究设计

研究类型
Interventional
分配方式
Randomized
主要目的
Treatment

入排标准

年龄范围
0 Years 至 120 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • DISEASE CHARACTERISTICS:
  • Diagnosis of post-transplant lymphoproliferative disease (PTLD) after solid organ (heart, heart/lung, liver, liver/gut, pancreas, or kidney) transplantation
  • Epstein-Barr virus-positive tumor
  • Newly diagnosed disease
  • Measurable disease by clinical methods or radiography
  • Must have partially matched donor cytotoxic T cells (CTL) available
  • No known panel reactivity to any of the HLA types of CTL available for therapy
  • PATIENT CHARACTERISTICS:
  • Performance status:
  • Karnofsky 20-100%
  • Life expectancy:
  • Not specified
  • Hematopoietic:
  • Not specified
  • Not specified
  • Not specified
  • Not pregnant
  • PRIOR CONCURRENT THERAPY:
  • Biologic therapy:
  • Not specified
  • Chemotherapy:
  • Not specified
  • Endocrine therapy:
  • Not specified
  • Radiotherapy:
  • Not specified
  • Not specified
  • No prior therapy for PTLD
  • No concurrent antiviral drugs (e.g., acyclovir or ganciclovir) for PTLD

排除标准

  • 未提供

结局指标

主要结局

Complete response

Survival at 2 years

Partial response

Time to complete remission

Stable disease

Progressive disease

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (12)

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