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The study of decitabine combination with aclarubicin and cytarabine and granulocyte colony-stimulating factor on the outcome of elderly patients with acute myeloid leukaemia

The study of decitabine combination with aclarubicin and cytarabine and granulocyte colony-stimulating factor on the outcome of elderly patients with acute myeloid leukaemia

Status
Recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-11001700
Enrollment
Unknown
Registered
2011-09-28
Start date
2011-09-15
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

acute myeloid leukemia in elder patients

Interventions

Case series:decitabine, cytarabine, aclarubicin, granulocyte colony-stimulating factor

Sponsors

The First Affiliated Hospital of Nanjing Medical Hospital, Jiangsu Province Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Men and women, aged between 60 to 75 years (non-APL); 2. ECOG performance status (PS) score 0-2; 3. Adequate hepatic funcetion defined as: (1) Total bilirubin 60ml/min; (4) Myocardial enzyme <2.0 times the institutional ULN; (5) cardiac ejection fraction in the normal range; 4. Patients understand the disease and voluntarily received the study regimen and follow-up; 5. Have signed the informed consent before study.

Exclusion criteria

Exclusion criteria: 1. A serious uncontrolled cardiac, renal or hepatic insufficiency; 2. Concurrent other malignant tumors other than AML; 3. History of significant bleeding disorder unrelated to AML; 4. A serious infection or metabolic disease; 5. Dementia or altered mental status that would prohibit the understanding or rendering of informed consent; 6. have a large operation within 21 day; 7. The patients with AIDS; 8. Researchers considered not join into the group; 9. Have known to any component of decitabine allergy.

Design outcomes

Primary

MeasureTime frame
CR, PR;

Secondary

MeasureTime frame
disease-free survival;

Countries

China

Contacts

Public ContactLi Jianyong
lijianyonglm@medmail.com.cn+86 13951877733

Outcome results

None listed

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