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临床试验/NCT03297476
NCT03297476已完成不适用

Early Precision Diagnosis and Relapse Prediction Technology Development in High-risk Acute Leukemia and Clinical Application

Zhongda Hospital1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2017年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100
试验地点
1
主要终点
complete remission

研究概览

简要总结

Based on the investigator's previous data on risk classification for acute leukemia,the investigators will design a set of panels to detect the gene expression and genomic variants (SNPs, mutation, insertion, deletion and fusion genes, etc), and identify the high-risk subtypes of acute leukemia, such as Ph-like acute lymphoblastic leukemia. Furthermore, the target therapy (Tyrosine Kinase Inhibitors,et.al) will be used to treat the identified patients. In addition, more sensitive minimal residual disease (MRD) detection technology will be designed and used to detect the MRD in patients to early predict the disease relapse.

详细描述

patient eligibility criteria: newly diagnosed acute leukemia patients with clinical high-risk markers, reflactory and relapsed patients.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
14 Years 至 75 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Newly diagnostic acute lymphoblastic leukemia Be willing to start treatment

排除标准

  • chronic leukemia

结局指标

主要结局

complete remission

时间窗: From date of randomization or initial treatment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 months

Patients achieve complete remission after initial treatment

relapse

时间窗: From date of randomization or complete remission until the date of first documented relapse from any cause, whichever came first, assessed up to 100 weeks

Patients' disease progress after complete remission

次要结局

未报告次要终点

研究者

发起方
Zhongda Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ge Zheng

Director of Hematology Department

Zhongda Hospital

研究点 (1)

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