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Clinical efficacy and adverse reactions analysis of combination therapy of Venetoclax and hypomethylated drugs in the treatment of acute myeloid leukemia: a retrospective multi-center clinical study in the real world.

Clinical efficacy and adverse reactions analysis of combination therapy of Venetoclax and hypomethylated drugs in the treatment of acute myeloid leukemia: a retrospective multi-center clinical study in the real world.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400090821
Enrollment
Unknown
Registered
2024-10-14
Start date
2024-04-16
Completion date
Unknown
Last updated
2024-10-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute myeloid leukemia

Interventions

Bone marrow remission group :No interventions
Bone marrow unrelieved group:No interventions

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Acute myeloid leukemia was confirmed; 2.It was first treated with Venetoclax combined with hypomethylatied drugs,with or without FLT-3 inhibitor.3.The ineligibility for standard chemo-therapy was determined if the patient matches at least one of the following: (1) 75 years of age or older; (2) one or more of pre-existing conditions including heart failure, chronic stable angina, lung function insufficiency, invasive pulmonary fungal infection and serious infection; (3) an Eastern Cooperative Oncology Group (ECOG) performance-status score of 2 or 4.

Exclusion criteria

Exclusion criteria: 1. The Venetoclax was used for less than seven days; 2.Concurrent use of cytotoxic drugs,lenalidomide and Chidamide should be excluded.;3.Patient who had previously used Venetoclax were excluded,4.Patient who have undergone hematopoietic stem cell transplantation should be excluded.5.Patients with disease in remission should be excluded. 6.Patient without sufficient clinical data .

Design outcomes

Primary

MeasureTime frame
Bone marrow remission degree;minimal residual disease;

Secondary

MeasureTime frame
Major hematological adverse events;

Countries

China

Contacts

Public ContactQingshu Zeng

Department of Hematology, The First Affiliated Hospital of Anhui Medical University

1414350126@qq.com+86 138 0551 4560

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026