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Optimization and promotion of precise diagnostic and treatment protocols for acute myeloid leukemia in children and adolescents

Optimization and promotion of precise diagnostic and treatment protocols for acute myeloid leukemia in children and adolescents

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078979
Enrollment
Unknown
Registered
2023-12-22
Start date
2023-12-31
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Acute myeloid leukemia in children and adolescents

Interventions

AML-nonAPL Venetoclax+CRNIT GROUP:The combination of targeted therapy and chemotherapy was applied in the treatment of reduction of volume, induction therapy, consolidation therapy and maintenance the
AML-nonAPL CRNIT GROUP:The combination of targeted therapy and chemotherapy was applied in the treatment of reduction of volume, induction therapy, consolidation therapy and maintenance therapy, and o
APL GROUP:Venetoclax was routinely used for APL reduction therapy, arsenic agent combined with ATRA was applied in induction therapy, consolidation therapy and maintenance therapy, and for patients wh

Sponsors

Beijing Children's Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed of AML; 2. Patients younger than 18 years old; 3. Patients who haven't received pre-treatment, except for those who receive single IT injection or Hydroxycarbamide or low-dose Ara-c for Leukocytosis (no more than 300mg/m2); 4. Patients or/and their guardian who have signed the Informed Consent Form.

Exclusion criteria

Exclusion criteria: 1. Junior Myelomonocytic Leukemia; 2. Mixed Phenotype Acute Leukemia; 3. Patients who received any anti-tumor treatment within 2 weeks, except for those who received single IT injection or Hydroxycarbamide or low-dose Ara-c for Leukocytosi; 4. Patients complicated with any other diseases or psychiatric disease that could affect their safety and compliance, informed consent, participation, follow-up or interpretation of results.

Design outcomes

Primary

MeasureTime frame
MRD;Bone marrow remission status;Drug toxicity;

Countries

China

Contacts

Public ContactHuyong Zheng

Beijing Children's Hospital, Capital Medical University

zhenghuyong@vip.sina.com+86 133 7011 5036

Outcome results

None listed

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