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

Author:

Reed Damon R.1,Grohar Patrick2,Rubin Elyssa3,Binitie Odion4,Krailo Mark5,Davis Jessica6ORCID,DuBois Steven G.7ORCID,Janeway Katherine A.7ORCID

Affiliation:

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

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

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

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

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

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

7. Dana‐Farber/Boston Children's Cancer and Blood Disorders Center Boston Massachusetts USA

Abstract

AbstractThe 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.

Funder

National Institutes of Health

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

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