Hispanic Children Hospitalized With Acute Lymphoblastic Leukemia Are at Increased Risk of Pancreatitis

Beth Savage1, Peter D Cole, Haiqun Lin

  • 1Author Affiliations: Rutgers University School of Nursing, Newark (Drs Savage, Lin, and Thomas-Hawkins); Rutgers Cancer Institute of New Jersey, New Brunswick (Dr Cole), NJ.

Cancer Nursing
|August 11, 2020
PubMed

Insights

Hispanic children with acute lymphoblastic leukemia face a higher risk of pancreatitis. This finding highlights potential genetic and social factors contributing to this disparity in pediatric cancer treatment.

Area of Science:

  • Pediatric Oncology
  • Hematology
  • Clinical Research

Background:

  • Childhood acute lymphoblastic leukemia (ALL) survival has improved, yet treatment toxicities like pancreatitis persist.
  • Pancreatitis often occurs early in ALL treatment, suggesting pre-existing risk factors beyond chemotherapy exposure.
  • The influence of race and ethnicity on treatment-related pancreatitis in pediatric ALL is not well understood.

Purpose of the Study:

  • To investigate the association between race/ethnicity and pancreatitis incidence in children diagnosed with ALL in the U.S.
  • To identify potential disparities in pancreatitis risk among diverse pediatric populations undergoing ALL treatment.

Main Methods:

  • Analysis of a national pediatric hospitalization database (21,775 ALL cases).
  • Descriptive statistics, chi-squared tests, and multilevel logistic regression models were employed.
  • Examined hospital discharge records for documented pancreatitis diagnoses.

Main Results:

  • Pancreatitis was identified in 1.6% of pediatric ALL hospitalizations.
  • Hispanic children demonstrated a significantly increased risk of pancreatitis compared to white children (P = .002).
  • No significant differences in pancreatitis risk were observed for Black, Asian, or other racial/ethnic groups.

Conclusions:

  • Hispanic children hospitalized with ALL exhibit a heightened risk of developing pancreatitis.
  • This disparity may stem from a combination of genetic predispositions and socioeconomic factors.
  • Further research into diverse patient populations is crucial for understanding and mitigating ALL treatment toxicities.
Abstract

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