Chidamide, Venetoclax, Azacitidine, and Homoharringtonine for High-risk Fit AML
A Single-arm, Single-center Clinical Trial Evaluating the Efficacy and Safety of a Regimen Combining Chidamide With Venetoclax, Azacitidine, and Homoharringtonine in the Treatment of Intermediate- to High-risk Fit AML Patients
研究概览
研究类型
注册 (估计的)
阶段
- 阶段2
联系人和位置
学习联系方式
- 姓名:Zhangkun Li
- 电话号码:0769-28637333
- 邮箱:lzk8239@163.com
参与标准
资格标准
适合学习的年龄
- 成人
接受健康志愿者
描述
Inclusion Criteria:
- Newly diagnosed fit-AML patients classified per the World Health Organization (WHO) classification criteria.
- Age ranging from 18 to 60 years, no restriction on gender.
- No prior anti-AML systemic therapy after AML diagnosis; cytoreductive treatment (e.g., hydroxyurea or cytarabine at a daily dose <1.0 g) is permitted as exception.
- Estimated overall survival ≥12 weeks.
- Eastern Cooperative Oncology Group (ECOG) performance status ≤3 points.
- Renal function: calculated creatinine clearance (CrCl) ≥30 mL/min.
- Hepatic function: alanine aminotransferase (ALT) <5× upper limit of normal (ULN); total bilirubin <3× ULN.
- Able to provide written informed consent and understand as well as comply with all study-specified procedures.
Exclusion Criteria:
- Patients stratified as favorable-risk AML defined by NCCN Guidelines 2022, including cytogenetic aberrations: t(8;21)(q22;q22.1); RUNX1-RUNX1T1, inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11.
- Confirmed acute promyelocytic leukemia (APL). AML complicated with central nervous system (CNS) leukemia infiltration.
- Cardiac function exceeding NYHA functional class II.
Confirmed human immunodeficiency virus (HIV) infection or other uncontrolled clinically significant comorbidities, including but not limited to:
- Uncontrolled or active systemic infection (viral, bacterial or fungal); ② Concurrent second primary malignancy requiring urgent clinical intervention.
6. Patients unable to receive oral chidamide and/or venetoclax administration. 7. Known hypersensitivity to any investigational product. 8. Pregnant or breastfeeding female subjects. 9. Inability to understand or adhere to the study protocol requirements. 10.Subjects deemed unsuitable for enrollment at the investigator's discretion
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Chidamide , Venetoclax, Azacitidine, Homoharringtonine
|
Induction (Chi+VAH Regimen): Cycle 1: Chi+VAH regimen (28-day cycle). Assessment & Cycle 2: CR/CRi: Repeat one cycle → Proceed to post-remission therapy. PR: Repeat one cycle → Re-assess. If CR/CRi → Proceed to post-remission therapy. NR: Discontinue study. Post-Remission / Consolidation: 1-2 cycles of either intermediate-dose Cytarabine (± targeted therapy) OR the Chi+VAH regimen. Eligible patients should proceed to allogeneic HSCT. Maintenance (Non-transplant): MRD-negative: VA (Venetoclax + Azacitidine) until relapse, intolerance, or 1 year. MRD-positive: Chi+VAH or clinical trial until MRD negativity, then switch to VA maintenance. |
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Composite Complete Remission Rate (CR+CRi)
大体时间:the First Induction Cycle (28days)
|
the First Induction Cycle (28days)
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
MRD negativity rate after the first induction cycle
大体时间:28 days
|
28 days
|
|
Composite CR/CRi rate after the second induction cycle
大体时间:56 days
|
56 days
|
|
2-year overall survival (OS) rate
大体时间:2 years
|
2 years
|
|
2-year relapse-free survival (RFS) rate
大体时间:2 years
|
2 years
|
|
Bridging Rate to Allo-HSCT
大体时间:2 years
|
2 years
|
|
Non-relapse mortality (NRM)
大体时间:2 years
|
2 years
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.