Why the study?
The impact of targeted strategies in improving synovial sarcoma outcomes remains limited, requiring further research into epigenomic regulation, biomarkers, and therapeutic targets to improve patient survival.
New molecular insights in synovial sarcoma, particularly in epigenomics and gene regulation, offer promising perspectives for novel diagnostic markers and therapeutic targets.
May guide epigenomic target exploration in synovial sarcoma; leaves open clinical validation before practice change.
OPINION STATEMENT: New molecular insights are being achieved in synovial sarcoma (SS) that can provide new potential diagnostic and prognostic markers as well as therapeutic targets. In particular, the advancement of research on epigenomics and gene regulation is promising. The concrete hypothesis that the pathogenesis of SS might mainly depend on the disruption of the balance of the complex interaction between epigenomic regulatory complexes and the consequences on gene expression opens interesting new perspectives. The standard of care for primary SS is wide surgical resection combined with radiation in selected cases. The role of chemotherapy is still under refinement and can be considered in patients at high risk of metastasis or in those with advanced disease. Cytotoxic chemotherapy (anthracyclines, ifosfamide, trabectedin, and pazopanib) is the treatment of choice, despite several possible side effects. Many possible drug-able targets have been identified. However, the impact of these strategies in improving SS outcome is still limited, thus making current and future research strongly needed to improve the survival of patients with SS.
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Fiore et al. (2021) studied this question.
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