Paving the Way for Immunotherapy in Pediatric Acute Myeloid Leukemia: Current Knowledge and the Way Forward.

acute myeloid leukemia children immune landscape immune monitoring immune profiling immunotherapy tumor immune microenvironment

Journal

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

Informations de publication

Date de publication:
28 Aug 2021
Historique:
received: 26 07 2021
revised: 22 08 2021
accepted: 26 08 2021
entrez: 10 9 2021
pubmed: 11 9 2021
medline: 11 9 2021
Statut: epublish

Résumé

Immunotherapeutic agents may be an attractive option to further improve outcomes and to reduce treatment-related toxicity for pediatric AML. While improvements in outcome have been observed with immunotherapy in many cancer types, immunotherapy development and implementation into patient care for both adult and pediatric AML has been hampered by an incomplete understanding of the bone marrow environment and a paucity of tumor-specific antigens. Since only a minority of patients respond in most immunotherapy trials across different cancer types, it will be crucial to understand which children with AML are likely to respond to or may benefit from immunotherapies. Immune cell profiling efforts hold promise to answer this question, as illustrated by the development of predictive scores in solid cancers. Such information on the number and phenotype of immune cells during current treatment regimens will be pivotal to generate hypotheses on how and when to intervene with immunotherapy in pediatric AML. In this review, we discuss the current understanding of the number and phenotype of immune cells in the bone marrow in pediatric AML, ongoing immunotherapy trials and how comprehensive immune profiling efforts may pave the way for successful clinical trials (and, ultimately, implementation into patient care).

Identifiants

pubmed: 34503174
pii: cancers13174364
doi: 10.3390/cancers13174364
pmc: PMC8431730
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : Stichting Kinderen Kankervrij
ID : 329

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Auteurs

Joost B Koedijk (JB)

Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.

Inge van der Werf (I)

Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.

Friso G Calkoen (FG)

Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.

Stefan Nierkens (S)

Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Center for Translational Immunology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.

Gertjan J L Kaspers (GJL)

Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Department of Pediatric Oncology, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit, 1105 AZ Amsterdam, The Netherlands.

Christian Michel Zwaan (CM)

Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Department of Pediatric Oncology, Erasmus MC/Sophia Children's Hospital, 3015 GD Rotterdam, The Netherlands.

Olaf Heidenreich (O)

Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands.
Wolfson Childhood Cancer Research Centre, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.

Classifications MeSH