Ethnic disparities relative to disease features and outcomes in children with acute myeloid leukemia

M Monica Gramatges1, Aditya Deshpande2, Philip J Lupo1,2

  • 1Texas Children's Cancer and Hematology Centers, Baylor College of Medicine, Houston, Texas.

Insights

Hispanic children with acute myeloid leukemia (AML) have worse outcomes than non-Hispanic white children, even with favorable genetic markers. This survival gap is linked to poorer results after stem cell transplantation in Hispanic children.

Area of Science:

  • Pediatric Hematology Oncology
  • Cancer Disparities Research
  • Clinical Outcomes Analysis

Background:

  • Hispanic children with acute leukemias exhibit poorer outcomes compared to non-Hispanic whites (NHWs).
  • This disparity persists despite a higher prevalence of favorable prognostic indicators in Hispanic pediatric patients.
  • Understanding the factors contributing to these differential outcomes is crucial for improving treatment strategies.

Purpose of the Study:

  • To investigate the survival outcomes of Hispanic and NHW children diagnosed with de novo acute myeloid leukemia (AML).
  • To determine if favorable cytogenetic features, such as t(8;21), translate into survival benefits for Hispanic children.
  • To identify potential reasons for observed survival differences, particularly concerning treatment modalities like stem cell transplantation.

Main Methods:

  • Retrospective review of medical records for 167 children (ages 0-18) with de novo AML.
  • Analysis focused on 129 self-identified Hispanic or NHW patients treated at Texas Children's Cancer Center over 18 years.
  • Comparison of event-free survival (EFS) and overall survival (OS) between ethnic groups, stratified by treatment, including upfront stem cell transplantation (SCT).

Main Results:

  • Hispanic children were significantly more likely to possess the favorable t(8;21) cytogenetic feature (P = 0.04).
  • Despite this, the expected survival advantage associated with t(8;21) was not observed in the Hispanic cohort.
  • Significantly poorer EFS and OS were noted among Hispanic children undergoing upfront SCT post-remission (P = 0.008), explaining the survival gap.

Conclusions:

  • Favorable cytogenetic markers do not confer the expected survival benefit for Hispanic children with AML.
  • Upfront stem cell transplantation in first remission is associated with inferior outcomes in Hispanic pediatric AML patients.
  • Further research is needed to address treatment-related factors contributing to ethnic disparities in pediatric AML survival.

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