Relapses Children's Acute Lymphoblastic Leukemia, Single Center Experience
Weronika Stolpa1, Magdalena Zapała2, Bartosz Zwiernik2
1Department of Oncology, Hematology and Chemotherapy, Upper Silesia Children's Care Heatlh Centre, 16 Medykow Street, 40-752 Katowice, Poland.
Children (Basel, Switzerland)
|December 23, 2022
Summary
Relapsed acute lymphoblastic leukemia (ALL) in children remains challenging. Early relapse timing and T-cell ALL are key factors impacting survival rates, necessitating improved risk stratification for personalized treatment.
Area of Science:
- Pediatric Oncology
- Hematology
- Cancer Research
Background:
- Relapsed acute lymphoblastic leukemia (ALL) in pediatric patients presents a significant therapeutic challenge, even with advanced treatments like hematopoietic stem cell transplantation.
- Identifying prognostic factors is crucial for improving outcomes in children and adolescents with relapsed ALL.
Purpose of the Study:
- To analyze the incidence of relapsed ALL in pediatric patients.
- To evaluate survival rates in correlation with identified risk factors.
- To determine the impact of relapse timing and leukemia subtype on prognosis.
Main Methods:
- Retrospective analysis of 125 pediatric ALL patients diagnosed between 2000-2018.
- Data collection included patient demographics, relapse details (timing, site), and survival outcomes.
- Statistical analysis to correlate risk factors with five-year overall survival.
Main Results:
- A relapse incidence of 15.2% was observed among pediatric ALL patients.
- Early relapse timing (63.1%) was more common than very early (15.8%) or late (21.1%) relapses.
- Five-year survival was achieved by 31.6% of patients, with a significant association between relapse type and survival (p < 0.05).
- Patients with very early relapses had a 0% five-year survival rate.
Conclusions:
- The timing of relapse onset is a primary prognostic factor in pediatric ALL.
- T-lineage ALL is identified as a significant adverse prognostic indicator.
- Integrating relapse risk factors with cytogenetic markers and minimal residual disease assessment is vital for optimizing first-line chemotherapy and personalizing ALL treatment strategies.


