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临床试验/NCT00118196
NCT00118196终止2 期

A Phase II Study of Arsenic Trioxide in Combination With 5-Azacitidine in Myelodysplastic Syndromes

Medical University of South Carolina2 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2005年4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 (overall and confirmed) as measured by International Working Group (IWG) standardized criteria for MDS at day 113 and then every 4 weeks until completion of study treatment

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy, such as azacitidine and arsenic trioxide, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more cancer cells.

PURPOSE: This phase II trial is studying how well giving azacitidine together with arsenic trioxide works in treating patients with myelodysplastic syndromes or chronic myelomonocytic leukemia.

详细描述

OBJECTIVES:

Primary

  • Determine the response rate in patients with myelodysplastic syndromes or chronic myelomonocytic leukemia treated with azacitidine and arsenic trioxide.

Secondary

  • Determine time to treatment failure in patients treated with this regimen.
  • Determine the tolerability and toxicity of this regimen in these patients.
  • Determine progression-free survival of patients treated with this regimen.

研究设计

研究类型
Interventional
分配方式
Non Randomized
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 120 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 (overall and confirmed) as measured by International Working Group (IWG) standardized criteria for MDS at day 113 and then every 4 weeks until completion of study treatment

次要结局

  • Time to treatment failure as assessed by the Kaplan-Meier method at completion of study treatment
  • Toxicity as assessed by the Kaplan-Meier method and NCI-CTCAE version 3.0 during treatment until 30 days after completion of study treatment
  • Progression-free survival as assessed by the Kaplan-Meier method at completion of study treatment

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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