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Insidious iron burden in pediatric patients with acute lymphoblastic leukemia
Jennifer Eng1, Jonathan D Fish
1Pediatric Hematology/Oncology and Stem Cell Transplantation, Steven and Alexandra Cohen Children's Medical Center of New York, New Hyde Park, New York, USA.
Insights
Pediatric patients with acute lymphoblastic leukemia (ALL) accumulate significant iron from blood transfusions. High-risk ALL patients receive the most iron, warranting iron overload screening during follow-up.
Area of Science:
- Pediatric Hematology Oncology
- Transfusion Medicine
- Iron Metabolism
Background:
- Hematologic disorders, particularly acute lymphoblastic leukemia (ALL), often necessitate frequent blood transfusions.
- Significant iron burden can accumulate after a limited number of transfusions, posing a risk to patients.
- Quantifying transfusion-related iron load in pediatric ALL patients is crucial for understanding long-term health implications.
Purpose of the Study:
- To quantify the volume of transfused blood and resultant iron load in a large cohort of pediatric patients with ALL.
- To evaluate risk factors, such as ALL risk category, that influence transfusion volume.
- To assess the correlation between patient characteristics and blood transfusion volumes.
Main Methods:
- A retrospective study was conducted on 107 pediatric patients who completed ALL therapy.
- Data collected included age, weight, hemoglobin at presentation, ALL risk category, and blood transfusion volumes.
- Statistical analysis was performed to identify associations between variables.
Main Results:
- Patients received an average of 115 ml/kg of blood, equating to 77 mg/kg of iron.
- A significant association was found between packed red blood cell volume and ALL risk category.
- High-risk ALL patients received substantially more iron (196 ml/kg) compared to standard-risk (90 ml/kg) or T-cell ALL (114 ml/kg) patients.
Conclusions:
- Pediatric patients with ALL accumulate a substantial iron load during therapy, with higher-risk patients bearing the greatest burden.
- Iron overload shares toxicity with chemotherapy and is treatable, suggesting the need for screening.
- Screening for iron burden and related morbidities should be considered in long-term ALL follow-up, especially for high-risk cases.
Background:
A significant iron burden may occur after only 10 blood transfusions in patients with hematologic disorders. Children with acute lymphoblastic leukemia (ALL) routinely receive blood transfusions during therapy, although few studies to date have quantified transfusion-related iron burden in these patients. This study quantifies the transfused blood volume and resultant iron load in a large cohort of pediatric patients with ALL, and evaluates risk factors that may impact transfusion volume.
Methods:
This single institution retrospective study evaluated 107 patients who completed therapy for ALL between July 1995 and March 2007. Age, weight, and hemoglobin at presentation, ALL risk category, leukemia cell type, and volume of blood transfusions were collected from medical records.
Results:
Patients received an average of 115 ml/kg of blood (77 mg/kg iron) during treatment. There was a significant association between the volume of packed red blood cells and ALL risk category. Patients with standard-risk disease received 90 ml/kg (60 mg/kg iron), patients with high-risk disease 196 ml/kg (131 mg/kg iron) and patients with T-cell disease 114 ml/kg (76 mg/kg iron). There was no correlation between age or hemoglobin at presentation with amount of blood received.
Conclusions:
Patients with ALL often receive a substantial amount of iron during therapy, with patients with high-risk disease receiving the greatest load. As iron overload has an overlapping toxicity profile with chemotherapy and is treatable, screening for increased iron burden and iron-related morbidities should be considered during long-term follow-up of patients with ALL, particularly in those with high-risk ALL.
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