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Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
Causes of Death in Childhood Acute Lymphoblastic Leukemia: A Single-Center Experience
Matej Jelić1, Maja Pavlović1, Lucija Mucavac1
1Division of Hematology and Oncology, Department of Pediatrics, University Hospital Center Zagreb, Kispaticeva 12, 10000 Zagreb, Croatia.
Insights
Relapse and infections are the main causes of death in pediatric acute lymphoblastic leukemia (ALL). Survival outcomes are significantly influenced by relapse timing and risk group, especially during induction and reinduction phases.
Area of Science:
- Pediatric Oncology
- Hematology
- Clinical Research
Background:
- Acute lymphoblastic leukemia (ALL) is a prevalent childhood cancer.
- Survival rates have improved due to advancements in risk stratification, therapy, and supportive care.
Purpose of the Study:
- To review epidemiology, prognostic factors, and causes of death in pediatric ALL.
- To identify risk factors impacting clinical outcomes in pediatric ALL patients.
Main Methods:
- Retrospective study of 302 children (0-18 years) diagnosed with ALL.
- Data collected from January 2001 to December 2015 at a tertiary care center.
Main Results:
- Overall survival was 83% (251 survivors).
- Relapse occurred in 13.6% of patients; higher in B-cell precursor (Bcp)-ALL than T-cell ALL.
- Main causes of death: refractory/relapsed disease (43%), infections (35%), GVHD (8%).
- Pseudomonas aeruginosa and Aspergillus fumigatus were frequent infectious causes of death.
- Relapse timing and risk group independently predicted outcome; no relapsed T-cell ALL survivors.
Conclusions:
- Relapse and infections are leading causes of mortality in pediatric ALL.
- Highest mortality observed during induction and reinduction phases.
- Relapse timing and risk group significantly influence survival in pediatric ALL.
Abstract:
Acute lymphoblastic leukemia (ALL) is the most common malignancy in children. Good overall survival rates of about 90% are the result of improvements in risk stratification and risk-adapted therapy, intensive chemotherapy regimens, hematopoietic stem cell transplantation, and better supportive care. Background and Objectives: The aim of this study is to review the epidemiology, prognostic factors, and causes of death in pediatric ALL patients treated at a tertiary care center, and to identify risk factors influencing clinical outcomes. Materials and Methods: A retrospective study was conducted at the Department of Pediatric Hematology and Oncology, University Hospital Centre Zagreb, including 302 children (0-18 years) diagnosed with ALL between January 2001 and December 2015. Results: Two hundred fifty-one children survived (5-year overall survival 83%). Relapse occurred in 13.6% of patients. Relapse rates were higher for B-cell precursor (Bcp)-ALL than for T-cell ALL (14.3% vs. 10.4%), and no patient with relapsed T-cell ALL survived. The main causes of death were refractory/relapsed disease (43% of patients), followed by infections (35%) and GVHD (8%). The most frequent causes of infectious death were Pseudomonas aeruginosa and Aspergillus fumigatus. The most critical treatment periods were the induction and reinduction phases, especially the de-escalation of corticosteroids. The time of relapse and risk group were independent factors in predicting the outcome. Conclusions: Relapse and infections were the leading causes of death in children with ALL, with the highest mortality observed during induction and reinduction phases. Survival was significantly influenced by relapse timing and risk group, with no survivors among relapsed T-ALL patients.
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