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临床试验/NCT05814731
NCT05814731尚未招募不适用

A Randomized Controlled Study on the Efficacy and Safety of MA-BUCY2 Protocol in the Conditioning of Haploidentical Stem Cell Transplantation in Patients With High-risk Acute Myeloid Leukemia

First Affiliated Hospital Xi'an Jiaotong University1 个研究点 分布在 1 个国家目标入组 264 人开始时间: 2023年4月15日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
尚未招募
入组人数
264
试验地点
1
主要终点
relapse rates

研究概览

简要总结

According to the 2022 ELN guidelines patients with high-risk acute myeloid leukemia were randomly divided into MA-BUCY2 conditioning group and BuCy2 conditioning group,to evaluate the efficacy and safety of two conditioning regimens in haploidentical hematopoietic stem cell transplantation.

详细描述

High risk acute myeloid leukemia patients were randomly divided into two groups before conditioning of haploidentical hematopoietic stem cell transplantation.The control group will use the BUCY2 conditioning,and the experimental group will use mitoxantrone liposome combined with BUCY2 for conditioning. After transplantation,we will observe the difference of one year relapse rates between two goups,also the adverse reactions of conditioning,GVHD,OS and PFS of the patients in two groups also been observed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Meet the diagnostic criteria of 2022 ELN guidelines for high-risk acute myeloid leukemia;
  • Patients with allogeneic stem cell transplantation indications;
  • Age 18-60 (including upper and lower limits) ;
  • No gender limit;
  • ECOG score 0~2 points;
  • Flow MRD was negative before transplantation;
  • The organ function level must meet the following requirements: a) Liver: aspartate aminotransferase (AST), alanine aminotransferase (ALT) ≤ 3 times the upper limit of normal value (ULN), Total bilirubin (TBIL) ≤ 1.5 × ULN; b) Kidney: blood creatinine ≤ 1.5 × ULN; c) Coagulation function: international normalized ratio (INR) and activated partial thromboplastin time (APTT) ≤ 1.5 × ULN; d) Normal cardiac function: that is, the ECG is normal or abnormal without clinical significance, and the left ventricular ejection fraction (LVEF) is greater than 60 or myocardial zymogram CK-MB is normal, pro-BNP is less than 900 pg/ml;
  • The results of serum pregnancy test of female subjects with reproductive ability must be negative before the first use of the test drug;

排除标准

  • Previously received doxorubicin or other anthracycline drugs, and the total cumulative dose of doxorubicin was more than 360 mg/m2;
  • Hypersensitivity to any study drug or its components;
  • Cardiac function and disease meet one of the following conditions:
  • Long QTc syndrome or QTc interval>480 ms;
  • Complete left bundle branch block, II or III degree atrioventricular block;
  • Serious and uncontrolled arrhythmia requiring drug treatment;
  • American New York Heart Association rating ≥ III;
  • Cardiac ejection fraction (LVEF) is less than 60%;
  • History of myocardial infarction, unstable angina pectoris, severe unstable ventricular arrhythmia or He has any arrhythmia requiring treatment, clinical history of serious pericardial disease, or acute ischemia or activity ECG evidence of abnormal conduction system.;\
  • Active infection of hepatitis B and hepatitis C;
  • Human immunodeficiency virus (HIV) infection;
  • Patients with other malignant tumors;
  • Pregnant and lactating women and patients of childbearing age who are unwilling to take contraceptive measures;
  • Have a history of abuse of drugs;
  • History of mental illness or cognitive impairment; .Other researchers judged that it was not suitable for this study.

研究组 & 干预措施

MA-BUCY2

Experimental

Mitoxantrone liposome 20mg/m2,ivgtt,d-11 ;Ara-C 4g/m2.d ,ivgtt,d-10- -9; BU 0.8 mg/kg q6h,ivgtt,d-8- -6; CTX 1.8 g/m2.d ,ivgtt,d-5- -4; me-CCNU 250 mg/m2,p.o,d-3; ATG 2.5 mg/Kg.d,d-5 -2;

干预措施: MA-BUCY2 (Drug)

BUCY2

Active Comparator

Ara-C 4g/m2.d ,ivgtt,d-10- -9; BU 0.8 mg/kg q6h,ivgtt,d-8- -6; CTX 1.8 g/m2.d ,ivgtt,d-5- -4; me-CCNU 250 mg/m2,p.o,d-3; ATG 2.5 mg/Kg.d,d-5 -2;

干预措施: BUCY2 (Drug)

结局指标

主要结局

relapse rates

时间窗: one year after transplantation

blast cells in bone marrow are greater than or equal to 5%. Blast cells can be seen in peripheral blood or extramedullary relapse occurred.

次要结局

  • aGVHD(At day 100 post-transplantation)
  • AEs(from beginning of the conditioning to one month after conditioning)
  • OS(From date of diagnosis until the end of follow-up or the date of death from any cause, whichever came first,assessed up to 36 months.)
  • PFS(From date of HSCT until the end of follow-up or the date of disease relapse from any cause, whichever came first,assessed up to 36 months.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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