Children's Oncology Group's 2023 blueprint for research: Bone tumors.


Journal

Pediatric blood & cancer
ISSN: 1545-5017
Titre abrégé: Pediatr Blood Cancer
Pays: United States
ID NLM: 101186624

Informations de publication

Date de publication:
09 2023
Historique:
received: 07 07 2023
accepted: 08 07 2023
pmc-release: 01 09 2024
medline: 18 8 2023
pubmed: 28 7 2023
entrez: 28 7 2023
Statut: ppublish

Résumé

The Children's Oncology Group (COG) Bone Tumor Committee is responsible for clinical trials and biological research on localized, metastatic, and recurrent osteosarcoma and Ewing sarcoma (EWS). Results of clinical trials in localized disease completed and published in the past 10 years have led to international standard-of-care chemotherapy for osteosarcoma and EWS. A recent focus on identifying disease subgroups has led to the identification of biological features associated with poor outcomes including the presence of circulating tumor DNA (ctDNA) at diagnosis, and specific genomic alterations-MYC amplification for osteosarcoma and STAG2 and TP53 mutation for EWS. Studies validating these potential biomarkers are under way. Clinical trials evaluating the addition of multitargeted kinase inhibitors, which are active in relapsed bone sarcomas, to standard chemotherapy are under way in osteosarcoma and planned in EWS. In addition, the Committee has data analyses and a clinical trial under way to evaluate approaches to local management of the primary tumor and metastatic sites. Given the rarity of bone sarcomas, we have prioritized international interactions and are in the process of forming an international data-sharing consortium to facilitate refinement of risk stratification and study of rare disease subtypes.

Identifiants

pubmed: 37501549
doi: 10.1002/pbc.30583
pmc: PMC10499366
mid: NIHMS1916211
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e30583

Subventions

Organisme : NCI NIH HHS
ID : U24 CA196173
Pays : United States
Organisme : NIH HHS
ID : U10CA098543
Pays : United States
Organisme : NIH HHS
ID : U24CA114766
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA098543
Pays : United States
Organisme : NIH HHS
ID : U10CA180884
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 : U10 CA098413
Pays : United States
Organisme : NIH HHS
ID : U10CA180899
Pays : United States
Organisme : NIH HHS
ID : U10CA180886
Pays : United States
Organisme : NCI NIH HHS
ID : U24 CA114766
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180884
Pays : United States
Organisme : NIH HHS
ID : U24CA196173
Pays : United States
Organisme : NIH HHS
ID : U10CA098413
Pays : United States

Informations de copyright

© 2023 Wiley Periodicals LLC.

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Auteurs

Damon R Reed (DR)

Department of Individualized Cancer Management, Moffitt Cancer Center, Tampa, Florida, USA.

Patrick Grohar (P)

Division of Oncology, Children's Hospital of Philadelphia Research Institute, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Elyssa Rubin (E)

Department of Oncology, Children's Hospital of Orange County, Orange, California, USA.

Odion Binitie (O)

Department of Sarcoma, Moffitt Cancer Center, Tampa, Florida, USA.

Mark Krailo (M)

Keck School of Medicine, University of Southern California and Children's Oncology Group, Monrovia, California, USA.

Jessica Davis (J)

Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.

Steven G DuBois (SG)

Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts, USA.

Katherine A Janeway (KA)

Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts, USA.

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