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临床试验/NCT00958854
NCT00958854Unknown2 期

Phase II Trial of Fludarabine & Cyclophosphamide Followed by Thalidomide for Angioimmunoblastic Lymphoma

Cancer Research UK2 个研究点 分布在 1 个国家目标入组 37 人开始时间: 2006年1月最近更新:
适应症
相关药物

试验速览

阶段
2 期
入组人数
37
试验地点
2
主要终点
Response rate after chemotherapy with fludarabine and cyclophosphamide

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy, such as fludarabine and cyclophosphamide, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Thalidomide may stop the growth of lymphoma by blocking blood flow to the cancer. Giving fludarabine and cyclophosphamide together with thalidomide may kill more cancer cells.

PURPOSE: This phase II trial is studying how well giving fludarabine and cyclophosphamide together with thalidomide works in treating patients with angioimmunoblastic T-cell lymphoma.

详细描述

OBJECTIVES:

Primary

  • Determine the response rate in patients with angioimmunoblastic T-cell lymphoma after chemotherapy comprising fludarabine and cyclophosphamide.

Secondary

  • Assess the incremental anatomical and molecular response rate in these patients during treatment with thalidomide.
  • Determine the toxicity of treatment with fludarabine and cyclophosphamide followed by thalidomide.
  • Assess the progression-free and overall survival of these patients.
  • Develop a detailed pathological description of the disease at presentation and at relapse.
  • Assess the number of circulating clonal T cells at presentation and during thalidomide treatment.
  • Screen for possible etiological viruses at presentation.
  • Evaluate the evolution of EBV viral load during follow-up.

研究设计

研究类型
Interventional
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(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 after chemotherapy with fludarabine and cyclophosphamide

次要结局

  • Incremental response rate to thalidomide treatment
  • Toxicity according to the NCI CTCAE v.3.0
  • Progression-free and overall survival

研究者

申办方类型
Other

研究点 (2)

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