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A single-arm prospective study on treatment of myelodysplastic syndromes and acute myeloid leukemia associated with myelodysplastic syndromes with chemotherapy plus HLA mismatched peripheral blood stem cell transplantation

A single-arm prospective study on treatment of myelodysplastic syndromes and acute myeloid leukemia associated with myelodysplastic syndromes with chemotherapy plus HLA mismatched peripheral blood stem cell transplantation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-17011948
Enrollment
Unknown
Registered
2017-07-11
Start date
2017-08-01
Completion date
Unknown
Last updated
2017-07-17

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

Conditions

Myelodysplastic syndromes and

Interventions

study group:chemotherapy plus HLA-mismatched donor's hematopoitic stem cells infusion

Sponsors

Bone Marrow Transplantation Center of the First Affiliated Hospital,College of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients are diagnosed as AML-MRC and High-risk MDS according to the 2016 WHO diagnostic criteria; 2. Patients are not suitable or not willing to undergo allogeneic hematopoietic stem cell transplantation; 3. Patients are willing to bear the cost of decitabine and does not have decitabine allergy histor; 4. Patients have suitable donor willing to donate stem cells (HLA haploidentical or not matched healthy donors; 5. Patients or legal representative have signed informed consent before clinical study start.

Exclusion criteria

Exclusion criteria: 1. Patients does not meet the diagnostic criteria; 2. patients with severe liver and kidney function, cardiorespiratory insufficiency; 3. uncontrolled or severe infection; 4. there may be a mental illness that may prevent subjects from completing treatment or informed consent.

Design outcomes

Primary

MeasureTime frame
complete remission;1 year's OS;2-year OS;

Secondary

MeasureTime frame
partial remission;total response rate;relapse rate;

Countries

China

Contacts

Public ContactJie Sun

Bone Marrow Transplantation Center of the First Affiliated Hospital,College of Medicine,Zhejiang University

jsun1492@zju.edu.cn+86 15305714109

Outcome results

None listed

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