Blood Count Recovery Following Induction Therapy for Acute Myeloid Leukemia in Children Does Not Predict Survival.

IWG criteria childhood acute myeloid leukemia clinical trial response assessment pediatric acute myeloid leukemia

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
26 Jan 2022
Historique:
received: 22 11 2021
revised: 18 01 2022
accepted: 21 01 2022
entrez: 15 2 2022
pubmed: 16 2 2022
medline: 16 2 2022
Statut: epublish

Résumé

International Working Group (IWG) and European LeukemiaNet (ELN) response definitions are utilized to evaluate the efficacy of new agents for childhood acute myeloid leukemia (AML) for regulatory purposes. However, these criteria are not consistent with definitions used in pediatric AML trials or with standard pediatric practice to proceed with subsequent therapy cycles prior to IWG/ELN-defined count recovery. We retrospectively analyzed data from the two most recent Phase 3 pediatric AML clinical trials conducted by the Children's Oncology Group (COG) to assess the incidence, timing, and prognostic significance of count recovery following induction chemotherapy. Of the patients with fewer than 5% bone marrow blasts at the end of first induction, 21.5% of patients proceeded to a second induction cycle prior to achieving ANC ≥ 500 cells/μL and platelets ≥ 50,000 cells/μL, both well below the IWG/ELN thresholds of ANC > 1000 cells/μL and platelets > 100,000 cells/μL. In these two sequential childhood AML Phase 3 trials, neither ANC nor platelet recovery predicted survival. Intensification of treatment through the initiation of subsequent therapy cycles prior to attainment of IWG/ELN-defined CR is common practice in clinical trials for children with AML, suggesting that updated response definitions are needed for pediatric AML.

Identifiants

pubmed: 35158884
pii: cancers14030616
doi: 10.3390/cancers14030616
pmc: PMC8833679
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

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

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Auteurs

Lauren Pommert (L)

Division of Oncology, Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA.

Todd M Cooper (TM)

Division of Hematology/Oncology, Cancer and Blood Disorders Center, Seattle Children's Hospital, Seattle, WA 98105, USA.

Robert B Gerbing (RB)

Children's Oncology Group, Monrovia, CA 91016, USA.

Lisa Brodersen (L)

Hematologics Inc., Seattle, WA 98121, USA.

Michael Loken (M)

Hematologics Inc., Seattle, WA 98121, USA.

Alan Gamis (A)

Children's Mercy Hospital and Clinics, Kansas City, MO 64108, USA.

Richard Aplenc (R)

Division of Oncology, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Todd A Alonzo (TA)

Department of Population and Public Health Sciences, University of Southern California, Los Angeles, CA 90032, USA.

Edward Anders Kolb (EA)

Nemours Center for Cancer and Blood Disorders/Nemours Children's Health, Wilmington, DE 19803, USA.

Classifications MeSH