CD123 Expression Is Associated With High-Risk Disease Characteristics in Childhood Acute Myeloid Leukemia: A Report From the Children's Oncology Group.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
20 01 2022
Historique:
pubmed: 3 12 2021
medline: 22 2 2022
entrez: 2 12 2021
Statut: ppublish

Résumé

Increased CD123 surface expression has been associated with high-risk disease characteristics in adult acute myeloid leukemia (AML), but has not been well-characterized in childhood AML. In this study, we defined CD123 expression and associated clinical characteristics in a uniformly treated cohort of pediatric patients with newly diagnosed AML enrolled on the Children's Oncology Group AAML1031 phase III trial (NCT01371981). AML blasts within diagnostic bone marrow specimens (n = 1,040) were prospectively analyzed for CD123 protein expression by multidimensional flow cytometry immunophenotyping at a central clinical laboratory. Patients were stratified as low-risk or high-risk on the basis of (1) leukemia-associated cytogenetic and molecular alterations and (2) end-of-induction measurable residual disease levels. The study population was divided into CD123 expression-based quartiles (n = 260 each) for analysis. Those with highest CD123 expression (quartile 4 [Q4]) had higher prevalence of high-risk CD123 is strongly associated with disease-relevant cytogenetic and molecular alterations in childhood AML. CD123 is a critical biomarker and promising immunotherapeutic target for children with relapsed or refractory AML, given its prevalent expression and enrichment in patients with high-risk genetic alterations and inferior clinical outcomes with conventional therapy.

Identifiants

pubmed: 34855461
doi: 10.1200/JCO.21.01595
pmc: PMC8769096
doi:

Substances chimiques

Biomarkers, Tumor 0
IL3RA protein, human 0
Interleukin-3 Receptor alpha Subunit 0

Banques de données

ClinicalTrials.gov
['NCT01371981']

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

252-261

Subventions

Organisme : NCI NIH HHS
ID : U10 CA180886
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180899
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

Adam J Lamble (AJ)

Division of Hematology/Oncology, Seattle Children's Hospital, University of Washington, Seattle, WA.

Todd A Alonzo (TA)

Children's Oncology Group, Monrovia, CA.
University of Southern California, Keck School of Medicine, Los Angeles, CA.

Jim Wang (J)

Children's Oncology Group, Monrovia, CA.

Laura Pardo (L)

Hematologics Inc, Seattle, WA.

Lillian Sung (L)

Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, CA.

Todd M Cooper (TM)

Division of Hematology/Oncology, Seattle Children's Hospital, University of Washington, Seattle, WA.

E Anders Kolb (EA)

Division of Oncology, Nemours/Alfred I. Dupont Hospital for Children, Wilmington, DE.

Richard Aplenc (R)

Division of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, PA.
Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Sarah K Tasian (SK)

Division of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, PA.
Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Michael R Loken (MR)

Hematologics Inc, Seattle, WA.

Soheil Meshinchi (S)

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

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