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Study of optimizing induction chemotherapy for elderly patients with acute myeloid leukemia based on peripheral blasts clearance rate

Study of optimizing induction chemotherapy for elderly patients with acute myeloid leukemia based on peripheral blasts clearance rate during induction

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OIN-16008955
Enrollment
Unknown
Registered
2016-08-02
Start date
2016-09-01
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

Interventions

Study Group:IDA

Sponsors

Rui Jin hospital affiliated to Shanghai Jiaotong University School of Medicine, Shanghai Institute of Hematology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Newly diagnosed elderly AML is confirmed by bone marrow morphology and immunology assay; 2. APL is excluded by bone marrow morphology or molecular level tests; 3. Patient is between the age of 60-75 years (including 60 and 75); 4. Bone marrow morphology demonstrates the features of active bone marrow hyperplasia; 5. Patient meets the conditions of Pre-treatment risk assessment stratification scale ("suitable " group) for elderly AML (non-M3); 6. Obtained an Informed Consent Form signed by patient or their families.

Exclusion criteria

Exclusion criteria: 1. APL patients; 2. Re-treated patient; 3. Low bone marrow hyperplasia promoted by bone marrow cytological examination; 4. Allergy to any drug presented in study protocol; 5. Obvious contraindications to anthracycline chemotherapy drugs; 6. Patient meets the conditions of "not suitable" and "unfit for chemotherapy" in the Pre-treatment risk assessment stratification scale for elderly AML (non-M3); 7. Unable to understand or comply with the study protocol; 8. Previous intolerance or allergy to the similar drugs; 9. Patients below the age of 60 or over 75 (60 and 75 are not included); 10. Participating in other clinical investigation simultaneously; 11. Having any issue that may hinder the clinical trial.

Design outcomes

Primary

MeasureTime frame
Overall Survival;Disease Free Survival;

Secondary

MeasureTime frame
Complete Remission;Minimal residual disease;

Countries

China

Contacts

Public ContactJunmin Li

Department of Hematology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine

lijunmin@medmail.com.cn+86 13817712211

Outcome results

None listed

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