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临床试验/NCT00243009
NCT00243009终止2 期

Non-Myeloablative Allogeneic Hematopoietic Stem Cell Transplantation for the Treatment of Metastatic Renal Cell Carcinoma

OHSU Knight Cancer Institute2 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2005年6月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
1
试验地点
2
主要终点
Response rate (complete and partial response) at 6 and 12 months after transplantation

研究概览

简要总结

RATIONALE: Giving low doses of chemotherapy, such as fludarabine, and radiation therapy before a donor stem cell transplant helps stop the growth of cancer cells. It also stops the patient's immune system from rejecting the donor's stem cells. The donated stem cells may replace the patient's immune system and help destroy any remaining cancer cells (graft-versus-tumor effect). Sometimes the transplanted cells from a donor can also make an immune response against the body's normal cells. Giving cyclosporine and mycophenolate mofetil after transplant may stop this from happening.

PURPOSE: This phase II trial is studying how well giving fludarabine together with total-body irradiation works in treating patients who are undergoing a donor stem cell transplant for metastatic kidney cancer that cannot be removed by surgery.

详细描述

OBJECTIVES:

  • Determine the efficacy of nonmyeloablative conditioning comprising fludarabine and total-body irradiation followed by allogeneic hematopoietic stem cell transplantation, in terms of 6-month and 12-month response rate, in patients with unresectable metastatic renal cell carcinoma.

OUTLINE:

  • Nonmyeloablative conditioning regimen: Patients receive fludarabine IV on days -4 to -2 and total-body irradiation (TBI) on day 0.
  • Allogeneic hematopoietic stem cell transplantation (AHSCT): After TBI, patients undergo AHSCT on day 0.
  • Immunosuppression: Patients receive oral cyclosporine twice daily on days -3 to 56 followed by a taper until day 81. Patients also receive oral mycophenolate mofetil twice daily on days 0-27 (if patient has a related donor) OR three times daily on days 0-29 and then twice daily on days 30-149 followed by additional tapering until day 180 (if patient has an unrelated donor).

PROJECTED ACCRUAL: A total of 15 patients will be accrued for this study.

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 75 Years(Adult, Older 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

结局指标

主要结局

Response rate (complete and partial response) at 6 and 12 months after transplantation

次要结局

  • Severity of graft-vs-host-disease by Glucksburg Scale after transplantation for up to 5 years
  • Incidence of graft rejection based on donor chimerims after transplantation for up to 5 years
  • Non-relapse mortality as assessed by Kaplan-Meier after transplantation for up to 5 years
  • Disease-free survival as assessed by Kaplan-Meier after transplantation for up to 5 years
  • Overall survival as assessed by Kaplan-Meier after transplantation for up to 5 years
  • Toxicity as measured by CTC AE v 3.0 100 days after transplantation

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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