Leukemia, Myeloid, Acute, Refractory Leukemia, Relapsed Adult AML
Conditions
Keywords
refractory/relapsed acute myelogenous leukemia
Brief summary
The purpose of this study is to evaluate the safety and efficacy of Venetoclax Combining Chidamide and Azacitidine (VCA) in the Treatment of relapsed and/or refractory AML
Detailed description
Patients with relapsed and/or refractory AML have inferior outcomes. The regimen of Venetoclax and Azacitidine has been widely used in the treatment of RR AML and has proved to achieve CR rate of 30% \ 40%. However, the median duration of response (DOR) of this regimen is about one year. Chidamide is a histone deacetylase (HDAC) inhibitor and preclinical data showed adding low-dose Chidamide to venetoclax could significantly promoted apoptosis of leukemia cell lines. Meanwhile, the Venetoclax Combining Chidamide and Azacitidine (VCA) regimen was applied to 2 patients with refractory AML. This regimen was well tolerated and both patients achieved CR after one cycle. Thus, we register this clinical trial and evaluate the safety and efficacy of VCA regimen.
Interventions
DRUGvenetoclax combining chidamide and azacitidine (VCA)
information already included in arm/group descriptions
Sponsors
Fujian Provincial Hospital
Fujian Cancer Hospital
Zhangzhou manicipal hospital of Fujian Province
Jieyang People's Hospital
Dongguan People's Hospital
Huizhou Municipal Central Hospital
The First Affiliated Hospital of Xiamen University
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age ≥18 * Relapsed and refractory patients with acute myeloid leukemia via morphology and immunology * ECOG：0-2 * Life expectancy ≥ 3 months * Adequate laboratory parameters during the screening period as evidenced by the following: 1. Creatinine clearance≥30 mL/min and serum Creatinine ≤ 160µmol/L 2. ALT and AST ≤ 3 × upper limit of normal (ULN) 3. Able to understand and sign an informed consent form (ICF).
Exclusion criteria
* Diagnosis of acute promyelocytic leukemia (APL) * Central nervous system leukemia * Uncontrolled or significant cardiovascular disease, including any of the following: 1. Bradycardia of less than 50 beats per minute, unless the subject has a pacemaker; Diagnosis of or suspicion of long QT syndrome (including family history of long QT syndrome); 2. Systolic blood pressure ≥180 mmHg or diastolic blood pressure ≥110 mmHg; History of clinically relevant ventricular arrhythmias (eg, ventricular tachycardia, ventricular fibrillation, or Torsade de Pointes); 3. History of second (Mobitz II) or third degree heart block (subjects with pacemakers are eligible if they have no history of fainting or clinically relevant arrhythmias while using the pacemaker); 4. History of uncontrolled angina pectoris or myocardial infarction within 6 months prior to Screening; 5. History of New York Heart Association Class 3 or 4 heart failure; 6. Complete left bundle branch block; 7. Known history of left ventricular ejection fraction (LVEF) ≤45% or less than the institutional lower limit of normal; * Active acute or chronic systemic fungal, bacterial, or viral infection not well controlled by antifungal, antibacterial or antiviral therapy; * Suffered from other non-myeloid malignancies within 2 years, except adequately treated non-melanoma skin cancer, curatively treated in-situ disease, or other solid tumors curatively treated with no evidence of disease * Females who are pregnant or breastfeeding; * Mental disorders that hinder research participation * Previous solid organ transplantation (SCT treatment is allowed in advance, but if the patient has GVHD or is still receiving immunosuppression/GVHD treatment, it is not allowed) * Any other situation where the investigator believes that the patient should not participate in this trial
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Complete remission (CR) rate | 2 months | CR was \<5% marrow blasts by morphology |
| Overall response rate (ORR) | 2 months | ORR is defined as CR, CRi and PR. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| 1 year leukemia free survival (LFS) | 1 year from treatment initiation | Leukemia-free survival (LFS) is defined as survival without evidence of relapse from treatment initiation |
| 1year overall survival (OS) | 1 year from treatment initiation | Overall survival（OS）is defined as the time from treatment initiation to death from any cause. |
| Adverse events | 2 months | Adverse event is defined as any untoward medical occurrence associated with treatment |
Countries
China
Contacts
Primary ContactBing Xu, M.D.
Outcome results
None listed