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Clinical study for BHA combined with chemotherapy in the treatment of elderly patients with acute myeloid leukemia /high risk myelodysplastic syndrome

Clinical study for BHA combined with chemotherapy in the treatment of elderly patients with acute myeloid leukemia /high risk myelodysplastic syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000029772
Enrollment
Unknown
Registered
2020-02-13
Start date
2020-02-15
Completion date
Unknown
Last updated
2022-03-07

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

Conditions

Elderly patients with acute myeloid leukemia/high risk myelodysplastic syndrome

Interventions

Sponsors

The Second Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patient with acute myeloid leukemia (including MDS transformed AML and relapsed AML after treatment) aged 60 to 75 years old; 2. MDS and IPSS graded as moderate risk, or MDS-EB-1 and MDS-EB-2 as refractory anemia and RAEB (including mds-eb-1 and mds-eb-2); 3. No serious complications, such as liver failure, renal failure, heart failure; 4. For the patients whose peripheral blood leukocytes were less than 50x10^9/L at the beginning of induction therapy, no chemical therapy was performed except hydroxyurea before induction therapy; 5. There was no uncontrollable hypertension and diabetes; 6. Must be able to understand the protocol, follow the doctor's orders and obtain informed consent signed by the patient or family member.

Exclusion criteria

Exclusion criteria: 1. Those who are allergic to the test drug; 2. Use other anti leukemia therapy, such as radiotherapy, cell immunotherapy; 3. Participate in other clinical trials at the same time; 4. Patients with other types of malignant tumors; 5. Have psychosis or other diseases, unable to fully cooperate with the trial treatment or follow-up requirements; 6. Patients with uncontrolled active infection; 7. The active period of uncontrolled infectious diseases, such as HIV, HBV, HCV, active tuberculosis, etc; 8. Patients with central nervous system leukemia; 9. The investigator evaluated those who could not participate in the clinical trial.

Design outcomes

Primary

MeasureTime frame
Complete response rate ;

Secondary

MeasureTime frame
Drug safety;

Countries

China

Contacts

Public ContactYan Jinsong

The Second Affiliated Hospital of Dalian Medical University

yanjsdmu@126.com+86 17709871028

Outcome results

None listed

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