Treatment outcome in pediatric patients with T-ALL in Brazil

Ana Maria Marinho da Silva1, Valdenizia R Silva2, Alython Araújo Chung-Filho2

  • 1Fundação Oswaldo Cruz, Fiocruz, Instituto Gonçalo Moniz, Salvador, Bahia 40296-710, Brazil; Hospital Aristides Maltez, Salvador, Bahia 40285-000, Brazil.

Leukemia Research
|August 6, 2026
PubMed

Insights

Pediatric T-cell acute lymphoblastic leukemia (T-ALL) survival in Brazil is lower than in high-income countries, with infection being a major cause of death. Treatment protocol adaptations are crucial for improving outcomes in low- and middle-income countries.

Area of Science:

  • Pediatric Oncology
  • Hematology
  • Epidemiology

Background:

  • Treatment intensification has improved pediatric T-cell acute lymphoblastic leukemia (T-ALL) survival in high-income countries (HICs).
  • Limited data exist on T-ALL treatment outcomes in low- and middle-income countries (LMICs).
  • This study examines T-ALL survival and clinical factors in Brazil's public healthcare system.

Purpose of the Study:

  • To evaluate survival rates for pediatric T-cell acute lymphoblastic leukemia (T-ALL) in Brazil.
  • To identify clinical factors associated with survival outcomes in T-ALL patients.
  • To compare the effectiveness of different treatment protocols within the Brazilian healthcare context.

Main Methods:

  • Retrospective analysis of medical records from 86 pediatric T-ALL patients (0-19 years).
  • Data collected from four reference oncology centers in the Brazilian Unified Health System.
  • Inclusion of clinical, demographic, and laboratory variables.

Main Results:

  • Five-year overall survival (pOS) was 47% and event-free survival (pEFS) was 43.2%.
  • Infection was the leading cause of death (69.4%).
  • Adenomegaly at diagnosis correlated with lower survival; the GBTLI-HR protocol showed higher pOS (70.0%) compared to others.

Conclusions:

  • Brazilian pediatric T-ALL patients face higher mortality rates than those in HICs.
  • High infection rates significantly contribute to mortality.
  • Context-specific adaptations of intensive treatment protocols are necessary for LMICs.
Abstract

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