Impact of Asparaginase Discontinuation on Outcome in Childhood Acute Lymphoblastic 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:
10 06 2020
Historique:
pubmed: 11 4 2020
medline: 23 2 2021
entrez: 11 4 2020
Statut: ppublish

Résumé

Asparaginase (ASNase) is an important component of acute lymphoblastic leukemia (ALL) treatment, but is often discontinued because of toxicity. Patients aged 1-30.99 years in frontline Children's Oncology Group trials for B-cell acute lymphoblastic leukemia between 2004 and 2011 (National Cancer Institute [NCI] standard risk [SR]: AALL0331; NCI high risk: AALL0232) were included. The number of prescribed pegaspargase (PEG-ASNase) doses varied by trial and strata. Maintenance therapy did not contain ASNase. Landmark analyses at maintenance compared disease-free survival (DFS) among those receiving all prescribed PEG-ASNase doses versus switching to We included 5,195 AALL0331 and 3,001 AALL0232 patients. The cumulative incidence of PEG-ASNase discontinuation was 12.2% ± 4.6% in AALL0331 and 25.4% ± 0.8% in AALL0232. In multivariable analyses, NCI high-risk patients not receiving all prescribed ASNase doses had inferior DFS (hazard ratio [HR], 1.5; 95% CI, 1.2 to 1.9; Discontinuation of ASNase doses is associated with inferior DFS in higher-risk patients. Our results illustrate the severe consequences of

Identifiants

pubmed: 32275469
doi: 10.1200/JCO.19.03024
pmc: PMC7280050
doi:

Substances chimiques

Polyethylene Glycols 3WJQ0SDW1A
pegaspargase 7D96IR0PPM
Asparaginase EC 3.5.1.1

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1897-1905

Subventions

Organisme : NCI NIH HHS
ID : U10 CA098543
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180899
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180886
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233324
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA098413
Pays : United States

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Auteurs

Sumit Gupta (S)

Division of Hematology/Oncology, The Hospital for Sick Children, Toronto, Ontario, Canada.

Cindy Wang (C)

Department of Biostatistics, University of Florida, Gainesville, FL.

Elizabeth A Raetz (EA)

Primary Children's Hospital, Salt Lake City, UT.

Reuven Schore (R)

Children's National Medical Center, Washington, DC.

Wanda L Salzer (WL)

US Army Medical Research and Materiel Command, Fort Detrick, MD.

Eric C Larsen (EC)

Department of Pediatrics, Maine Children's Cancer Program, Scarborough, ME.

Kelly W Maloney (KW)

Children's Hospital Colorado, Aurora, CO.

Len A Mattano (LA)

Harpoon Therapeutics Pharma Consulting, Mystic, CT.

William L Carroll (WL)

Department of Pediatrics and Perlmutter Cancer Center, New York University Langone Health, New York, NY.

Naomi J Winick (NJ)

University of Texas Southwestern/Simmons Cancer Center, Dallas, TX.

Stephen P Hunger (SP)

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

Mignon L Loh (ML)

Department of Pediatrics, UCSF Benoiff Childen's Hospital and Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA.

Meenakshi Devidas (M)

Department of Global Pediatric Medicine, St Jude Children's Research Hospital, Memphis, TN.

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Classifications MeSH