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Multicenter study on the efficacy of four regimens containing homoharringtonine for refractory and relapsed acute myeloid leukemia

Multicenter study on the efficacy of four regimens containing homoharringtonine for refractory and relapsed acute myeloid leukemia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034336
Enrollment
Unknown
Registered
2020-07-02
Start date
2020-07-23
Completion date
Unknown
Last updated
2020-07-06

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

Conditions

Acute myeloid leukemia

Interventions

Group A:HAD scheme
Group B:CHG scheme
Group C:DHAD scheme
Group D:DCHG scheme

Sponsors

Shanxi Bethune Hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age: >= 18 years old and 5%; (3) extramedullary recurrence. 5. Inclusion criteria of had and Dhad regimens: AML patients with active hyperplasia or FLT3 / ITD +, FLT3 / TKD + were preferred to have regimen; If AML patients with a history of prodromal MDS or MPD, or with complex karyotypes (>= 3 kinds), or with typical methylation gene mutation, Dhad regimen (plus decitabine 15mg / m2 / D, D1-5) should be preferred. 6. Inclusion criteria of CHG and dchg regimens: Patients with AML whose myelogram showed decreased proliferation or whose white blood cells were lower than normal range were preferred to CHG regimen. If AML patients with a history of prodromal MDS or MPD, or with complex karyotypes (>= 3 kinds), or with typical methylation gene mutation, dchg regimen (plus decitabine 15mg / m2 / D, D1-5) should be preferred. 7. The ECOG-ps score of the eastern oncology collaboration group was 0-2. 8. Sign informed consent.

Exclusion criteria

Exclusion criteria: 1) Accompanied by cerebral hemorrhage; 2) Pregnancy; 3) Mental illness or other conditions that cannot be carried out as planned; 4) Severe arrhythmia, abnormal ECG (QT > 500ms).

Design outcomes

Primary

MeasureTime frame
Complete remission rate;Relapse Rate;Treatment related mortality;

Secondary

MeasureTime frame
Event free survival;Overall survival;Peripheral blood primitive cell count in agranulocytosis;Efficacy of different subgroups;Safety of chemotherapeutic drugs;

Countries

China

Contacts

Public ContactTao Wang

Shanxi Bethune Hospital of Shanxi Medical University

wangtao99699@163.com+86 13835175119

Outcome results

None listed

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