Genomic architecture and treatment outcome in pediatric acute myeloid leukemia: a Children’s Oncology Group report

Author:

Vujkovic Marijana1ORCID,Attiyeh Edward F.1,Ries Rhonda E.2ORCID,Goodman Elizabeth K.1,Ding Yang1,Kavcic Marko3,Alonzo Todd A.4ORCID,Wang Yi-Cheng5,Gerbing Robert B.5,Sung Lillian6ORCID,Hirsch Betsy7ORCID,Raimondi Susana18,Gamis Alan S.9ORCID,Meshinchi Soheil2ORCID,Aplenc Richard1ORCID

Affiliation:

1. Division of Oncology, Children’s Hospital of Philadelphia, Philadelphia, PA;

2. Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA;

3. Unit of Oncology and Hematology, University Medical Centre, Ljubljana, Slovenia;

4. Keck School of Medicine, University of Southern California, Los Angeles, CA;

5. Children’s Oncology Group, Monrovia, CA;

6. Hospital for Sick Kids, Toronto, ON, Canada;

7. Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN;

8. St Jude Children’s Research Hospital, Memphis, TN; and

9. Division of Hematology/Oncology/Bone Marrow Transplantation, Children’s Mercy Hospitals & Clinics, Kansas City, MO

Abstract

Key Points Pediatric patients with de novo AML on average acquire 1.14 somatic CNAs in a study sample of 446 patients. The presence of CNAs is significantly associated with survival in standard-risk patients.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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1. Ancillary Tests;Pediatric Pathology of Hematopoietic and Histiocytic Disorders;2024-02-15

2. Chromosomal and Genomic Alterations in Pediatric AML;Pediatric Oncology;2024

3. Using expression quantitative trait loci data and graph-embedded neural networks to uncover genotype–phenotype interactions;Frontiers in Genetics;2022-08-15

4. Acute myeloid leukemia;Lanzkowsky's Manual of Pediatric Hematology and Oncology;2022

5. Monosomal karyotype as an adverse risk factor for inferior survivals in children with acute myeloid leukemia;Pediatric Hematology Oncology Journal;2021-12

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