An MRD-stratified pediatric protocol is as deliverable in adolescents and young adults as in children with ALL.


Journal

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

Informations de publication

Date de publication:
28 12 2021
Historique:
received: 21 06 2021
accepted: 21 09 2021
pubmed: 19 10 2021
medline: 8 1 2022
entrez: 18 10 2021
Statut: ppublish

Résumé

Pediatric regimens have improved outcomes in adolescent and young adult (AYA) acute lymphoblastic leukemia (ALL). However, results remain inferior to children with ALL. The Australasian Leukaemia and Lymphoma Group (ALLG) ALL06 study (anzctr.org.au/ACTRN12611000814976) was designed to assess whether a pediatric ALL regimen (Australian and New Zealand Children's Haematology and Oncology Group [ANZCHOG] Study 8) could be administered to patients aged 15 to 39 years in a comparable time frame to children as assessed by the proportion of patients completing induction/consolidation and commencing the next phase of therapy (protocol M or high-risk [HR] treatment) by day 94. Minimal residual disease (MRD) response stratified patients to HR treatment and transplantation. From 2012 to 2018, a total of 86 patients were enrolled; 82 were eligible. Median age was 22 years (range, 16-38 years). Induction/consolidation was equally deliverable in ALL06 as in Study 8. In ALL06, 41.5% (95% confidence interval [CI], 30.7-52.9) commenced protocol M or HR therapy by day 94 vs 39.3% in Study 8 (P = .77). Median time to protocol M/HR treatment was 96 days (interquartile range, 87.5-103 days) in ALL06 vs 98 days in Study 8 (P = .80). Induction mortality was 3.6%. With a median follow-up of 44 months (1-96 months), estimated 3-year disease-free survival was 72.8% (95% CI, 62.8-82.7), and estimated 3-year overall survival was 74.9% (95% CI, 65.3-84.5). End induction/consolidation MRD negativity rate was 58.6%. Body mass index ≥30 kg/m2 and day 79 MRD positivity were associated with poorer disease-free survival and overall survival. Pediatric therapy was safe and as deliverable in AYA patients as in children with ALL. Intolerance of pediatric ALL induction/consolidation is not a major contributor to inferior outcomes in AYA ALL.

Identifiants

pubmed: 34662896
pii: 477382
doi: 10.1182/bloodadvances.2021005576
pmc: PMC8714725
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5574-5583

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2021 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.

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Auteurs

Matthew Greenwood (M)

Royal North Shore Hospital, St. Leonards, NSW, Australia.
Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.

Toby Trahair (T)

Children's Cancer Institute, Lowy Cancer Research Centre, University of New South Wales, Randwick, NSW, Australia.
Kids Cancer Centre, Sydney Children's Hospital, Randwick, NSW, Australia.

Rosemary Sutton (R)

Children's Cancer Institute, Lowy Cancer Research Centre, University of New South Wales, Randwick, NSW, Australia.
School of Women's and Children's Health, University of New South Wales Medicine, Randwick, NSW, Australia.

Michael Osborn (M)

Royal Adelaide Hospital, Adelaide, SA, Australia.

John Kwan (J)

Westmead Hospital, Westmead, NSW, Australia.

Sally Mapp (S)

Princess Alexandra Hospital, Brisbane, QLD, Australia.

Rebecca Howman (R)

Sir Charles Gairdner Hospital, Nedlands, WA, Australia.

Antoinette Anazodo (A)

Prince of Wales Hospital, Randwick, NSW, Australia.

Brenton Wylie (B)

Gosford Hospital, Gosford, NSW, Australia.

James D'Rozario (J)

Canberra Hospital, Garran, ACT, Australia.

Mark Hertzberg (M)

Prince of Wales Hospital, Randwick, NSW, Australia.

Ian Irving (I)

The Townsville Hospital, Townsville, QLD, Australia.

David Yeung (D)

Royal Adelaide Hospital, Adelaide, SA, Australia.

Luke Coyle (L)

Royal North Shore Hospital, St. Leonards, NSW, Australia.

Amanda Jager (A)

Australasian Leukaemia Lymphoma Group, Melbourne, VIC, Australia.

Dan Engeler (D)

Australasian Leukaemia Lymphoma Group, Melbourne, VIC, Australia.

Nicola Venn (N)

Children's Cancer Institute, Lowy Cancer Research Centre, University of New South Wales, Randwick, NSW, Australia.

Chris Frampton (C)

Department of Psychological Medicine, University of Otago, Christchurch, New Zealand.

Andrew H Wei (AH)

The Alfred Hospital and Monash University, Melbourne, VIC, Australia; and.

Kenneth Bradstock (K)

Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
Westmead Hospital, Westmead, NSW, Australia.

Luciano Dalla-Pozza (L)

Cancer Centre for Children, The Children's Hospital at Westmead, Westmead, NSW, Australia.

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Classifications MeSH