跳至主要内容
临床试验/NCT03902769
NCT03902769Unknown不适用

Phase II Prospective Study to Assess Rate for Prolonged Remission With Intensive Chemotherapy in Rapid Respondents AML Patients Younger Than 61 as Demonstrated by Day 5 Examination of the First Treatment.

Rambam Health Care Campus0 个研究点目标入组 160 人开始时间: 2019年4月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
160
主要终点
Event free survival

研究概览

简要总结

We previously reported results of a prospective observational study demonstrating that early response defined as reduction in bone marrow (BM) blast counts to less than 5% of BM cells by the fifth day of induction therapy is a strong predictor of remission and overall survival (Ofran Y, et al. AJH, 2015). The long term survival benefit of early response was confirmed later on after a median follow-up for surviving patients of 53 months (range 17.5-84.5).

详细描述

Patients diagnosed with AML, younger than 61 year of age assigned for intensive chemotherapy, and diagnosed with standard or intermediate risk AML, will undergo BM examination on the fifth day of induction. Patients in whom BM blast count at the fifth day of induction will be lower than 5% will proceed therapy with consolidations or autologous SCT with-holding the option for allo-SCT. MRD monitoring will apply to those with reliable molecular marker.

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 61 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • AML diagnosis,
  • treated with 3+7 Induction chemotherapy
  • Intermediate/standard risk AML

排除标准

  • Diagnosed of APL
  • high risk molecular/cytogenetic score

研究组 & 干预措施

No allogeneic SCT

Experimental

For standard or intermediate risk AML patients who achieved good rapid response, allogenic SCT will be excluded from treatment plan

干预措施: Prescribing conventional chemotherapy while with holding allo-SCT (Procedure)

Standard post induction therapy

Active Comparator

For slow responding AML patients, post induction therapy will be provided according to treating physician discretion

干预措施: Prescribing conventional chemotherapy while with holding allo-SCT (Procedure)

结局指标

主要结局

Event free survival

时间窗: Two years

次要结局

  • Overall survivial(two years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Yishai Ofran

Director of leukemia Service

Rambam Health Care Campus

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