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Published on: October 17, 2025
Pediatric relapsed acute myeloid leukemia: a systematic review
Anne E Hoffman1, Linda J Schoonmade2, Gertjan Jl Kaspers1,3
1Emma Children's Hospital, Amsterdam UMC, Pediatric Oncology, Vrije Universiteit Amsterdam , Amsterdam.
Treatment for pediatric relapsed acute myeloid leukemia (AML) lacks standardization. Duration of first complete remission is a key prognostic factor, and allogeneic stem cell transplant shows promise for consolidation therapy.
Area of Science:
- Pediatric Hematology/Oncology
- Cancer Treatment Outcomes
- Systematic Review Methodology
Background:
- Pediatric relapsed acute myeloid leukemia (AML) has a poor prognosis despite intensive therapies.
- Optimal treatment strategies and prognostic factors for relapsed pediatric AML are not well-defined.
- There is a significant lack of randomized clinical trials in this area.
Purpose of the Study:
- To systematically review existing literature on treatment outcomes for pediatric patients with relapsed AML.
- To identify prognostic factors and evaluate the effectiveness of different therapeutic approaches.
- To highlight gaps in knowledge and suggest future research directions.
Main Methods:
- Systematic literature search of PubMed and Embase.com.
- Inclusion criteria: pediatric patients (<21 years) with relapsed AML, reporting clinical outcomes.
- Analysis of 12 selected studies focusing on second complete remission (CR2), disease-free survival (DFS), event-free survival (EFS), and overall survival (OS).
Main Results:
- No standard treatment exists for relapsed pediatric AML.
- Reported CR2 rates averaged 64% (range 50-75%), and 2- to 10-year OS rates averaged 31% (range 16-43%).
- Chemotherapy alone in first complete remission (CR1) may yield better outcomes than allogeneic stem cell transplant (allo-SCT) in CR1; allo-SCT is effective for CR2 consolidation.
- Duration of CR1 was the most significant prognostic factor identified.
Conclusions:
- Pediatric relapsed AML treatment requires further research to establish standardized, risk-stratified therapies.
- Improved understanding of prognostic factors and development of more effective, less toxic treatments are crucial.
- International collaboration for large, randomized clinical trials is essential to address knowledge gaps.
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