Retrospective analysis of outcomes for pediatric acute lymphoblastic leukemia in South American centers
Caitlyn Duffy1, Dylan E Graetz1, Arturo M Zapata Lopez2
1St. Jude Children's Research Hospital, Department of Global Pediatric Medicine, Memphis, TN, United States.
Insights
Pediatric Acute Lymphoblastic Leukemia (ALL) survival in South America is lower than in high-income countries due to infections and treatment delays. New guidelines aim to improve outcomes for childhood ALL patients.
Area of Science:
- Pediatric Oncology
- Hematology
- Epidemiology
Background:
- Acute Lymphoblastic Leukemia (ALL) is the most common childhood cancer.
- Survival rates for pediatric ALL vary significantly between high-income and low-to-middle-income countries.
- Understanding regional disparities in pediatric ALL care is crucial for improving outcomes.
Purpose of the Study:
- To retrospectively analyze demographic, biological, and clinical data of pediatric ALL patients in South America.
- To identify factors affecting survival rates in this population.
- To inform the development of improved treatment guidelines.
Main Methods:
- Retrospective review of 752 pediatric ALL patients (2013-2017) across five centers in four South American countries.
- Analysis of diagnostic parameters, treatment interruptions, and survival outcomes.
- Kaplan-Meier method used for survival analyses.
Main Results:
- B-cell ALL (92.1%) and T-cell ALL (7.5%) were predominant subtypes.
- Advanced diagnostic availability varied; MRD evaluated in 69.1%, molecular testing in 75-81%, karyotyping in 42-61%.
- Chemotherapy delays (>2 weeks) occurred in 56.0% of patients, often due to infections (63.2%) or resource constraints (23.2%). Three-year EFS was 71.0% and OS was 79.6%.
Conclusions:
- Opportunities exist to improve pediatric ALL survival by addressing severe infections and treatment interruptions.
- Resource constraints and drug shortages significantly impact treatment delivery.
- The development of adapted treatment guidelines, like those by the POLA group, is essential for standardizing care and improving outcomes.
Introduction:
Acute lymphoblastic Leukemia (ALL) is the most common pediatric malignancy. While the survival rate for childhood ALL exceeds 90% in high-income countries, the estimated survival in low-and middle-income countries ranges from 22-79%, depending on the region and local resources.
Methods:
This study retrospectively reviewed demographic, biological, and clinical parameters of children under 18 years of age with newly diagnosed ALL presenting between 2013-2017 across five pediatric centers in 4 countries in South America. Survival analyses were estimated using the Kaplan-Meier method.
Results:
Across the five centers, 752 patients were analyzed (Bolivia [N=9], Ecuador [N=221], Paraguay [N=197], Peru [N=325]) and 92.1% (n=690) patients were diagnosed with B-cell and 7.5% (n= 56) with T-cell ALL. The median age was 5.5 years old (IQR 7.29). At diagnosis, 47.8% of patients were categorized as standard and 51.9% as high risk per their institutional regimen. Advanced diagnostics availability varied between modalities. MRD was evaluated in 69.1% of patients; molecular testing was available for ETV6-RUNX, BCR-ABL1, TCF3-PBX1, and KMT2A-rearranged ALL in 75-81% of patients; however, karyotyping and evaluation for iAMP21 were only performed in 42-61% of patients. Central nervous system (CNS) involvement was evaluated at diagnosis in 57.3% (n=429) patients; of these, 93.7% (n=402) were CNS 1, 1.6% (n=7) were CNS 2, 0.7% (n=11) were CNS3, 1.9% (n=8) had cranial nerve palsy, and 2.1% (n=9) results unavailable. Chemotherapy delays >2 weeks were reported in 56.0% (n=421) patients during treatment. Delays were attributed to infection in 63.2% (n=265), drug-related toxicities in 47.3% (n=198), and resource constraints, including lack of bed availability in 23.2% (n=97) of patients. The 3-year Abandonment-sensitive EFS and OS were 61.0±1.9% and 67.2±1.8%, respectively. The 3-year EFS and OS were 71.0±1.8% and 79.6±1.7%, respectively.
Discussion:
This work reveals opportunities to improve survival, including addressing severe infections, treatment interruptions, and modifications due to drug shortages. In 2018, healthcare professionals across South America established the Pediatric Oncology Latin America (POLA) group in collaboration with St. Jude Children's Research Hospital. POLA collaborators developed an evidence-based, consensus-derived, adapted treatment guideline, informed by preliminary results of this evaluation, to serve as the new standard of care for pediatric ALL in participating institutions.
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