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Emerging Treatments Targeting the Tumor Microenvironment for Advanced Chondrosarcoma.
- Source :
-
Cells [Cells] 2024 Jun 04; Vol. 13 (11). Date of Electronic Publication: 2024 Jun 04. - Publication Year :
- 2024
-
Abstract
- Chondrosarcoma (ChS), a malignant cartilage-producing tumor, is the second most frequently diagnosed osseous sarcoma after osteosarcoma. It represents a very heterogeneous group of malignant chemo- and radiation-resistant neoplasms, accounting for approximately 20% of all bone sarcomas. The majority of ChS patients have a good prognosis after a complete surgical resection, as these tumors grow slowly and rarely metastasize. Conversely, patients with inoperable disease, due to the tumor location, size, or metastases, represent a great clinical challenge. Despite several genetic and epigenetic alterations that have been described in distinct ChS subtypes, very few therapeutic options are currently available for ChS patients. Therefore, new prognostic factors for tumor progression as well as new treatment options have to be explored, especially for patients with unresectable or metastatic disease. Recent studies have shown that a correlation between immune infiltrate composition, tumor aggressiveness, and survival does exist in ChS patients. In addition, the intra-tumor microvessel density has been proven to be associated with aggressive clinical behavior and a high metastatic potential in ChS. This review will provide an insight into the ChS microenvironment, since immunotherapy and antiangiogenic agents are emerging as interesting therapeutic options for ChS patients.
- Subjects :
- Humans
Bone Neoplasms pathology
Bone Neoplasms therapy
Bone Neoplasms metabolism
Bone Neoplasms genetics
Immunotherapy
Angiogenesis Inhibitors therapeutic use
Angiogenesis Inhibitors pharmacology
Chondrosarcoma pathology
Chondrosarcoma genetics
Chondrosarcoma metabolism
Tumor Microenvironment
Subjects
Details
- Language :
- English
- ISSN :
- 2073-4409
- Volume :
- 13
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Cells
- Publication Type :
- Academic Journal
- Accession number :
- 38891109
- Full Text :
- https://doi.org/10.3390/cells13110977