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Racial and ethnic differences in survival of children with acute lymphoblastic leukemia

Smita Bhatia1, Harland N Sather, Nyla A Heerema

  • 1Children's Oncology Group, City of Hope National Medical Center, PO Box 60012, Arcadia, CA 91006-6012, USA. sbhatia@coh.org

Blood
|August 30, 2002
PubMed

Insights

Racial and ethnic disparities persist in acute lymphoblastic leukemia (ALL) outcomes for children. Black and Hispanic children experienced worse survival, while Asian children had better outcomes, even with modern risk-based therapy.

Area of Science:

  • Pediatric Oncology
  • Hematology
  • Epidemiology

Background:

  • Black children with acute lymphoblastic leukemia (ALL) have poorer outcomes.
  • Limited data exists on outcomes for Hispanic and Asian children with ALL.
  • Understanding racial and ethnic disparities is crucial for equitable cancer care.

Purpose of the Study:

  • To determine outcomes for children with ALL across different racial and ethnic backgrounds.
  • To analyze survival rates adjusted for known prognostic factors.
  • To identify specific disparities in treatment response by ethnicity.

Main Methods:

  • Retrospective cohort study of 8447 children with newly diagnosed ALL (1983-1995).
  • Analysis of overall survival (OS) and event-free survival (EFS).
  • Multivariate analysis adjusting for clinical features, disease biology, socioeconomic status, and treatment era.

Main Results:

  • Significant differences in survival by ethnicity (P <.001).
  • Five-year EFS rates: Asian (75.1%), White (72.8%), Hispanic (65.9%), Black (61.5%).
  • Black and Hispanic children had worse outcomes; Asian children had better outcomes compared to White children, after adjustment.

Conclusions:

  • Racial and ethnic disparities in pediatric ALL outcomes persist despite contemporary risk-based therapy.
  • Poorer outcomes for Black children were most evident in standard-risk groups; for Hispanic children, in high-risk groups.
  • Asian children showed superior outcomes, particularly in high-risk and recent treatment eras, suggesting potential areas for further investigation into compliance or pharmacogenetics.

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