Biology of Bone Sarcomas and New Therapeutic Developments.
review · Level V
Where this comes from
- Record sourced from PubMed, PMID 29238848.
- Also identified by DOI 10.1007/s00223-017-0372-2 and PMC identifier 5805807.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Bone sarcomas are tumours belonging to the family of mesenchymal tumours and constitute a highly heterogeneous tumour group. The three main bone sarcomas are osteosarcoma, Ewing sarcoma and chondrosarcoma each subdivided in diverse histological entities. They are clinically characterised by a relatively high morbidity and mortality, especially in children and adolescents. Although these tumours are histologically, molecularly and genetically heterogeneous, they share a common involvement of the local microenvironment in their pathogenesis. This review gives a brief overview of their specificities and summarises the main therapeutic advances in the field of bone sarcoma.
Medical subject headings
- Bone Neoplasms
- Sarcoma