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Monitoring of autologous hematopoietic stem cell transplantation for elderly patients with intermediate and high risk acute myeloid leukemia based on second-generation flow cytometry and digital PCR

Monitoring of autologous hematopoietic stem cell transplantation for elderly patients with intermediate and high risk acute myeloid leukemia based on second-generation flow cytometry and digital PCR

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600115992
Enrollment
Unknown
Registered
2026-01-04
Start date
2026-01-04
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Acute Myeloid Leukemia

Interventions

Experimental group:Conditioning Regimens: (1) Busulfan/Cyclophosphamide (Bu/Cy): Bu: 3.2 mg·kg/1·d 1 × 2 days Cy: 50 mg·kg/1·d 1 × 2 days (2) Busulfan/Melphalan (Bu/Mel): Bu: 3.2 mg·kg/1·d 1 × 2 days

Sponsors

The First Affiliated Hospital of Xinjiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Middle- or high-risk AML patients aged over 60; 2. No suitable allo-HSCT donor or deemed unable to tolerate allo-HSCT; 3. Patients without severe organ damage in the heart, lungs, kidneys, or other functions, with only mild liver impairment (Child grade A); 4. Patients with hepatitis B or C but no active liver injury, who can undergo transplantation if viral replication is strictly monitored and kept below normal copy numbers; those with tuberculosis infection but controlled lesions, who can proceed with transplantation under ongoing anti-tuberculosis treatment; those with recent confirmed fungal infections but fully controlled lesions, who can undergo transplantation under intensified secondary antifungal prophylaxis; 5. Patients who voluntarily sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Age: less than 60 years; 2. Presence of uncontrolled active infections; 3. Impairment of heart, lung, or kidney function and severe liver damage (Child-Pugh Class B-C); 4. Mental illness; 5. Inability to sign an informed consent form.

Design outcomes

Primary

MeasureTime frame
Minimal residual disease;

Countries

China

Contacts

Public ContactYuan Hailong

The First Affiliated Hospital of Xinjiang Medical Universit

1074913015@qq.com+86 139 9996 1228

Outcome results

None listed

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