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Children's Oncology Group's 2023 blueprint for research: Bone tumors.
Reed, Damon R; Grohar, Patrick; Rubin, Elyssa; Binitie, Odion; Krailo, Mark; Davis, Jessica; DuBois, Steven G; Janeway, Katherine A.
Afiliação
  • Reed DR; Department of Individualized Cancer Management, Moffitt Cancer Center, Tampa, Florida, USA.
  • Grohar P; Division of Oncology, Children's Hospital of Philadelphia Research Institute, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Rubin E; Department of Oncology, Children's Hospital of Orange County, Orange, California, USA.
  • Binitie O; Department of Sarcoma, Moffitt Cancer Center, Tampa, Florida, USA.
  • Krailo M; Keck School of Medicine, University of Southern California and Children's Oncology Group, Monrovia, California, USA.
  • Davis J; Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
  • DuBois SG; Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts, USA.
  • Janeway KA; Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts, USA.
Pediatr Blood Cancer ; 70 Suppl 6: e30583, 2023 09.
Article em En | MEDLINE | ID: mdl-37501549
ABSTRACT
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoma de Ewing / Neoplasias Ósseas / Osteossarcoma / Tumores Neuroectodérmicos Primitivos Periféricos Limite: Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoma de Ewing / Neoplasias Ósseas / Osteossarcoma / Tumores Neuroectodérmicos Primitivos Periféricos Limite: Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article