Affiliations 

  • 1 Department of Pharmaceutical Sciences, St Jude Children's Research Hospital, Memphis, Tennessee
  • 2 National Pediatric Oncology Unit, Guatemala City, Guatemala
  • 3 Department of Biostatistics, St Jude Children's Research Hospital, Memphis, Tennessee
  • 4 Department of Pathology, St Jude Children's Research Hospital, Memphis, Tennessee
  • 5 Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore
  • 6 Department of Global Pediatric Medicine, St Jude Children's Research Hospital, Memphis, Tennessee
  • 7 Department of Paediatrics, Sime Darby Medical Centre Subang Jaya, Subang Jaya, Malaysia
  • 8 Department of Paediatrics, KK Women's and Children's Hospital, Singapore, Singapore
  • 9 Department of Paediatrics, University of Malaya Medical Centre, Kuala Lumpur, Malaysia
  • 10 Department of Pediatrics and Center for Childhood Cancer Research, Children's Hospital of Philadelphia and the Perelman School of Medicine at The University of Pennsylvania, Philadelphia
  • 11 Department of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee
  • 12 Department of Pediatrics, Benioff Children's Hospital and the Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco
  • 13 Khoo Teck Puat-National University Children's Medical Institute, National University Hospital, National University Health System, Singapore, Singapore
JAMA Oncol, 2022 Mar 01;8(3):354-363.
PMID: 35084434 DOI: 10.1001/jamaoncol.2021.6826

Abstract

IMPORTANCE: Racial and ethnic disparities persist in the incidence and treatment outcomes of childhood acute lymphoblastic leukemia (ALL). However, there is a paucity of data describing the genetic basis of these disparities, especially in association with modern ALL molecular taxonomy and in the context of contemporary treatment regimens.

OBJECTIVE: To evaluate the association of genetic ancestry with childhood ALL molecular subtypes and outcomes of modern ALL therapy.

DESIGN, SETTING, AND PARTICIPANTS: This multinational, multicenter genetic association study was conducted from March 1, 2000, to November 20, 2020, among 2428 children and adolescents with ALL enrolled in frontline trials from the United States, South East Asia (Singapore and Malaysia), and Latin America (Guatemala), representing diverse populations of European, African, Native American, East Asian, and South Asian descent. Statistical analysis was conducted from February 3, 2020, to April 19, 2021.

MAIN OUTCOMES AND MEASURES: Molecular subtypes of ALL and genetic ancestry were comprehensively characterized by performing RNA sequencing. Associations of genetic ancestries with ALL molecular subtypes and treatment outcomes were then evaluated.

RESULTS: Among the participants in the study, 1340 of 2318 (57.8%) were male, and the mean (SD) age was 7.8 (5.3) years. Of 21 ALL subtypes identified, 8 were associated with ancestry. East Asian ancestry was positively associated with the frequency of somatic DUX4 (odds ratio [OR], 1.30 [95% CI, 1.16-1.45]; P 

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.