A Multicenter, Single-Arm Clinical Study of the Venetoclax, Ivosidenib, and Azacitidine Triple-Drug Regimen in the Treatment of Chemotherapy-eligible Adult Patients With IDH1-Mutated Acute Myeloid Leukemia.
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 入组人数
- 23
- 试验地点
- 1
- 主要终点
- CRc rate
研究概览
简要总结
Venetoclax can bind to the BCL-2 protein, thereby initiating the apoptosis program and exerting anti-AML effects. The induction regimen combining venetoclax with hypomethylating agents (HMA) significantly improves the remission rate (over 60%) in elderly unfit AML patients and markedly prolongs survival in those achieving complete remission. Isocitrate dehydrogenase (IDH) 1 and 2 are involved in the citric acid cycle. Approximately 20% of AML patients carry IDH1 or IDH2 mutations, which lead to the reduction of α-ketoglutarate to 2-hydroxyglutarate (2-HG). 2-HG can cause histone methylation and inhibit TET2 activity, resulting in DNA hypermethylation, thereby affecting gene expression and cell differentiation. IDH mutations are more common in elderly patients and are often associated with cytogenetic abnormalities; they may also co-occur with FLT3-ITD, NPM1, or DNMT3A mutations. Ivosidenib is an IDH1 inhibitor, and previous studies have confirmed its safety and efficacy in AML treatment. According to adult AML treatment guidelines, IDH-mutated patients eligible for intensive chemotherapy may receive IDH inhibitors during induction therapy. Based on the study by Montesinos et al. on the role of ivosidenib and azacitidine in IDH-mutated AML, for patients ineligible for intensive chemotherapy, a new treatment option has been added: IDH1-mutated AML patients may receive ivosidenib (500 mg, days 1-28) combined with azacitidine (75 mg/m²/day for 7 days) in 28-day cycles, or ivosidenib monotherapy. Recent studies have shown that a triple-drug regimen comprising ivosidenib, venetoclax, and azacitidine demonstrates excellent efficacy and safety. In chemotherapy-ineligible patients, the triple regimen achieved a composite complete remission rate (CRc) of 86% and an overall response rate (ORR) of 92%. At a median follow-up of 27.4 months, the 2-year overall survival (OS) was 72%, and the 2-year event-free survival (EFS) was 72%. Therefore, this study aims to conduct a multicenter, single-arm clinical trial to preliminarily evaluate the long-term efficacy of this combination in adult AML.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 14 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients who meet AML according to WHO (2022) or AML and MDS/AML defined by ICC standards with IDH1 mutations detected by PCR or second-generation sequencing.
- •Age ≥14 years old, male or female.
- •The physical status assessment (ECOG-PS) of the Eastern Oncology Collaboration group was 0-2 points.
- •Fulfill the requirements of the following laboratory tests (performed within 7 days prior to treatment) :
- •Total bilirubin ≤ 1.5 times the upper limit of normal value (same age);
- •AST and ALT≤ 2.5 times the upper limit of normal value (same age);
- •Blood creatinine < 2 times the upper limit of normal (same age);
- •Myocardial enzymes < 2 times the upper limit of normal (same age);
- •Left ventricular ejection fraction >50% by measure of echocardiogram (ECHO) Informed consent must be signed before the commencement of all specific study procedures, and is signed by the patient himself or his immediate family. Considering the patient's condition, if the patient's signature is not conducive to the treatment of the condition, the informed consent shall be signed by the legal guardian or the patient's immediate family.
排除标准
- •Subjects who meet any of the following criteria are excluded from the study:
- •Acute promyelocytic leukemia with PML-RARA fusion gene
- •Acute myeloid leukemia with RUNX1-RUNX1T1 or CBFB-MYH11 fusion gene
- •Acute myeloid leukemia with BCR-ABL fusion gene
- •Treated patients (but can receive hydroxyurea or cytarabine to lower tumor burden).
- •Concurrent malignant tumors of other organs (those requiring treatment).
- •Active heart disease, defined as one or more of the following:
- •A history of uncontrolled or symptomatic angina;
- •Myocardial infarction less than 6 months after enrollment;
- •Have a history of arrhythmia requiring drug treatment or severe clinical symptoms;
- •Uncontrolled or symptomatic congestive heart failure (> NYHA level 2);
- •Serious infectious diseases (uncured tuberculosis, pulmonary aspergillosis).
- •Those who were not considered suitable for inclusion by the researchers.
研究组 & 干预措施
Venetoclax、Ivosidenib and Azacitidine
Induction regimen includes venetoclax, ivosidenib and azacitidine followed by consolidation therapy with intermediate dose of cytarabine.
干预措施: Ivosidenib, Venetoclax, Azacitidine (Drug)
结局指标
主要结局
CRc rate
时间窗: Efficacy was assessed at least 2 weeks after completion of the first course of induction therapy.
The ratio of patients achieved CR/CRh/CRi.
CRc MRD negtive rate by flow cytometry
时间窗: Efficacy was assessed at least 2 weeks after completion of the first course of induction therapy.
The CRc MRD negtive rate was detected by flow cytometry after induction, consolidation and maintenance therapy.
CRc MRD negtive rate by PCR
时间窗: Efficacy was assessed at least 2 weeks after completion of the first course of induction therapy.
The CRc MRD negtive rate was detected by PCR after induction, consolidation and maintenance therapy.
The maximum tolerated dose of ivosidenib and venetoclax combined with intensive chemotherapy
时间窗: up to 3 months after enrollment of the first participants
To determine the maximum tolerated dose of ivosidenib and venetoclax combined with intensive chemotherapy
次要结局
- Event-free survival (EFS)(up to 2 years after the date of the last enrolled participants)
- overall survival(up to 2 years after the date of the last enrolled participants)
- Relapse free survival(up to 2 years after the date of the last enrolled participants)
- 30-day mortality(Within 30 days of the date of the last enrolled participants)
- 60-day mortality(Within 60 days of the date of the last enrolled participants)