Comparison of CALGB 10403 (Alliance) and COG AALL0232 toxicity results in young adults with acute lymphoblastic leukemia.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
26 01 2021
Historique:
received: 22 06 2020
accepted: 30 11 2020
entrez: 26 1 2021
pubmed: 27 1 2021
medline: 15 5 2021
Statut: ppublish

Résumé

Adolescents and young adults (AYAs) with acute lymphoblastic leukemia have improved outcomes when treated with pediatric-inspired regimens. CALGB 10403 was the largest prospective study to evaluate the feasibility of using a pediatric regimen in AYAs with acute lymphoblastic leukemia up to 40 years of age. This article presents the toxicity events observed in the CALGB 10403 study and compares these toxicities vs those observed among AYAs treated on the same arm of the companion Children's Oncology Group (COG) AALL0232 study. Toxicities in CALGB 10403 were similar to those observed in COG AALL0232. Some grade 3 to 4 adverse events were more often reported in CALGB 10403 compared with COG AALL0232 (hyperglycemia, hyperbilirubinemia, transaminase elevation, and febrile neutropenia). Adverse events correlated with body mass index ≥30 kg/m2 and some with increasing age. The mortality rate in CALGB 10403 was low (4%) and similar to that in the COG AALL0232 trial. A caveat to this analysis is that only 39% of CALGB 10403 patients completed all planned protocol treatment. In COG AALL0232, although 74% of patients aged <18 years completed treatment, only 57% of patients aged ≥18 years completed treatment. This scenario suggests that issues associated with age and treating physician may be a factor. Due to its improved survival rates compared with historical controls, the CALGB 10403 regimen is now a standard of care. The hope is that the rate of protocol completion will increase as more familiarity is gained with this regimen. These trials were registered at www.clinicaltrials.gov as #NCT00558519 (CALGB 10403) and #NCT00075725 (COG AALL0232).

Identifiants

pubmed: 33496745
pii: S2473-9529(21)00071-9
doi: 10.1182/bloodadvances.2020002439
pmc: PMC7839367
doi:

Banques de données

ClinicalTrials.gov
['NCT00558519', 'NCT00075725']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

504-512

Subventions

Organisme : NCI NIH HHS
ID : U24 CA196173
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233290
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180821
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA098413
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233302
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233373
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233180
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180882
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180820
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180899
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233253
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233328
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233327
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA098543
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180888
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180886
Pays : United States

Informations de copyright

© 2021 by The American Society of Hematology.

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Auteurs

Anjali S Advani (AS)

Cleveland Clinic Taussig Cancer Institute, Cleveland, OH.

Eric Larsen (E)

Maine Children's Cancer Program, Scarborough, ME.

Kristina Laumann (K)

Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, MN.

Selina M Luger (SM)

University of Pennsylvania Abramson Cancer Center, Philadelphia, PA.

Michaela Liedtke (M)

Stanford Medical Center, Stanford, CA.

Meenakshi Devidas (M)

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

Zhiguo Chen (Z)

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

Jun Yin (J)

Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, MN.

Matthew C Foster (MC)

University of North Carolina Lineberger Comprehensive Cancer Center, Chapel Hill, NC.

David Claxton (D)

Penn State Cancer Institute, Hershey, PA.

Kristin Coffan (K)

Children's Hospital of Philadelphia, Pennsylvania, PA.

Martin S Tallman (MS)

Memorial Sloan-Kettering Cancer Center, New York, NY.

Frederick R Appelbaum (FR)

Fred Hutchinson Cancer Center; Seattle, WA.

Harry Erba (H)

Duke Cancer Institute, Duke University Medical Center, Durham, NC.

Richard M Stone (RM)

Dana-Farber/Partners CancerCare, Boston, MA.

Stephen P Hunger (SP)

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

Jennifer L McNeer (JL)

University of Chicago Comer Children's Hospital, Chicago, IL.

Mignon L Loh (ML)

Department of Pediatrics, Benioff Children's Hospital, and the Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA.

Elizabeth Raetz (E)

NYU Langone Health, New York, NY.

Naomi Winick (N)

University of Texas Southwestern Medical Center, Dallas, TX; and.

William Carroll (W)

NYU Langone Health, New York, NY.

Richard A Larson (RA)

University of Chicago Comprehensive Cancer Center, Chicago, IL.

Wendy Stock (W)

University of Chicago Comprehensive Cancer Center, Chicago, IL.

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Classifications MeSH