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Randomized Control Study on the Prognosis of AML/MDS Undergoing HSCT with a Decitabine Containing Conditioning Regimen Combined with Bu/Flu

Randomized Control Study on the Prognosis of AML/MDS Undergoing HSCT with a Decitabine Containing Conditioning Regimen Combined with Bu/Flu

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049223
Enrollment
Unknown
Registered
2021-07-26
Start date
2021-07-31
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

graft versus host disease

Interventions

experimental group:Decitabine containing condition regimen
control group:With no intervention of decitabine

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years; 2. Meet the diagnostic criteria for AML (2016WHO) and have allo-HSCT indications, or meet the MDS diagnostic criteria (2016WHO) and have allo-HSCT indications, with available donors, and no contraindications for transplantation; 3. Patients who are suitable for conventional Blu/Flu conditioning regimen; 4. No serious diseases of the heart, liver, kidney, lung and other important organs, no rheumatic immune diseases, endocrine diseases and other tumors, no history of chronic digestive tract diseases; 5. No smoking and alcohol addiction, history of drug abuse, body mass index (BMI) <27kg/m^2; 6. Regular follow-up, with good compliance, agree to participate in this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Second and above transplant recipients; 2. Patients with chronic kidney disease, pulmonary interstitial disease, etc. who need to take other immune preparations for a long time.

Design outcomes

Primary

MeasureTime frame
Incidence of GVHD;Leukemia recurrence rate;Overall survival during follow-up;Disease free survival;Median follow up time;

Countries

China

Contacts

Public ContactRen Hanyun

Peking University First Hospital

renhy0813@163.com+86 13910091592

Outcome results

None listed

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