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How I treat paediatric relapsed acute myeloid leukaemia
1Paediatric Oncology/Haematology, VU University Medical Center, Amsterdam, The Netherlands.
Insights
Relapsed paediatric acute myeloid leukaemia (AML) has a poor prognosis, with only 35% long-term survival despite intensive treatment. New strategies are crucial for improving outcomes in children with relapsed AML.
Area of Science:
- Pediatric Oncology
- Hematology
- Leukemia Research
Background:
- Paediatric acute myeloid leukaemia (AML) survival rates have improved, yet approximately one-third of patients experience relapse.
- Relapsed AML in children carries a poor prognosis, with limited long-term survival (around 35%) even with aggressive therapies like intensive chemotherapy and allogeneic stem cell transplantation.
- Current treatment regimens for relapsed paediatric AML are associated with significant toxicity and treatment-related mortality, highlighting the urgent need for therapeutic advancements.
Observation:
- Significant biological changes in AML cells can occur between initial diagnosis and relapse.
- Comprehensive diagnostic work-up is essential upon suspected relapse to identify these biological shifts.
- Practical challenges in managing relapsed paediatric AML require careful consideration.
Findings:
- The review synthesizes current knowledge on paediatric relapsed AML.
- It discusses various therapeutic possibilities and practical management issues.
- It emphasizes the need for improved treatment strategies to enhance survival rates.
Implications:
- Major improvements in treating paediatric relapsed AML are necessary.
- Understanding biological changes at relapse is key for tailored therapeutic approaches.
- This review provides insights for clinicians and translational researchers aiming to improve outcomes for children with relapsed AML.
Abstract:
The prognosis of paediatric acute myeloid leukaemia (AML) has improved significantly over the recent decades, but still about one-third of patients relapse. These patients have a relatively poor prognosis, with a probability of long-term survival from relapse of about 35%. This can only be achieved with very intensive chemotherapy and, usually, allogeneic stem cell transplantation, leading to very significant toxicity and even treatment-related mortality. Major improvements in the treatment of paediatric relapsed AML thus are required still, and several possibilities are discussed. In case of a suspected relapse, a comprehensive diagnostic work-up has to be undertaken, because significant changes in the biological features of the AML cells may have occurred between initial diagnosis and relapse. This review discusses many practical issues that one encounters in the treatment of children with relapsed AML. It will also be of interest for those involved in translational research in AML.
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