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临床试验/ChiCTR-OCH-12002406
ChiCTR-OCH-12002406已完成Unknown

Risk-stratification Treatment Directed by Minimal Residual Disease in Acute Myeloid Leukemia with t(8;21) in First Complete Remission

no0 个研究点目标入组 110 人开始时间: 2005年6月1日最近更新:

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
110
主要终点
relapse

研究概览

简要总结

To improve outcome in patients with t(8;21) acute myeloid leukemia(AML) in first complete remission (CR) by applying risk-directed therapy that was based on measurements of minimal residual disease (MRD) by quantitative PCR during treatment.

研究设计

研究类型
Observational

入排标准

年龄范围
14 至 60(—)
性别
All

入选标准

  • (1) newly diagnosed AML patients with a positive t(8;21) cytogenetic result or RUX1/RUX1T1 transcripts;
  • (2) between 14 and 60-years-old;
  • (3) in first complete remission (CR1);
  • (4) no contraindications to consolidation chemotherapy or HSCT.

排除标准

  • (1) relapsed AML patients with a positive t(8;21) cytogenetic result or RUX1/RUX1T1 transcripts;
  • (2) less than 14 or more than 60-years-old;
  • (3) in first complete remission (CR1);
  • (4) no contraindications to consolidation chemotherapy or HSCT.

研究组 & 干预措施

1

risk-directed treatment

结局指标

主要结局

relapse

DFS

次要结局

未报告次要终点

研究者

发起方
no

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