Abstract
Synovial sarcoma (SyS) occurs mostly in young adults and is characterized by an aggressive course. Combined treatment including chemotherapy, radiotherapy and surgical excision of the tumour is still not satisfactory, with mean 5-year survival of 30-50%. New targeted treatment options have appeared recently, e.g. HER2 and EGFR antagonists. Initial studies have revealed immunohistochemical overexpression of the EGFR in SyS; therefore trials with EGFR antagonist therapy have commenced. The aim of our study was to evaluate the status of HER2, EGFR and TOPIIA in SyS before and after combined therapy. Immunohistochemistry and FISH tests were performed. Significant discrepancies between protein expression and gene status were found. The authors discuss the potential reasons for that phenomenon.
MeSH terms
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Adolescent
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Adult
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Antineoplastic Agents / therapeutic use
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Combined Modality Therapy
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DNA Topoisomerases, Type II / genetics
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DNA Topoisomerases, Type II / metabolism*
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DNA-Binding Proteins / genetics
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DNA-Binding Proteins / metabolism*
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ErbB Receptors / genetics
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ErbB Receptors / metabolism*
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Female
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Gene Amplification
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Gene Expression Regulation, Neoplastic
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Humans
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Ifosfamide / therapeutic use
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Male
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Middle Aged
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Radiotherapy
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Receptor, ErbB-2 / genetics
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Receptor, ErbB-2 / metabolism*
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Sarcoma, Synovial / genetics
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Sarcoma, Synovial / metabolism*
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Sarcoma, Synovial / therapy*
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Soft Tissue Neoplasms / genetics
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Soft Tissue Neoplasms / metabolism*
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Soft Tissue Neoplasms / therapy*
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Young Adult
Substances
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Antineoplastic Agents
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DNA-Binding Proteins
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EGFR protein, human
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ERBB2 protein, human
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ErbB Receptors
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Receptor, ErbB-2
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DNA Topoisomerases, Type II
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Ifosfamide