Abstract
Synovial sarcoma is a rare soft tissue sarcoma characterized by a t(X;18) translocation, which results in a SYT-SSX gene fusion. In the metastatic setting, chemotherapy has limited, durable efficacy prompting the necessity for new therapeutic modalities. One emerging new strategy involves T-cell-directed therapy such as tumor-infiltrating lymphocytes or the development of T cells that are genetically engineered to express a T-cell receptor against a cancer testis antigen. Of these approaches, engineered T cells that recognize NY-ESO-1 are the furthest along in development. Completed and on-going clinical trials have shown promise and there are efforts to continue to optimize the current approach.
Keywords:
NY-ESO-1; adoptive T-cell therapy; chimeric antigen receptor; engineered T cell; synovial sarcoma; tumor-infiltrating lymphocytes.
MeSH terms
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Antigens, Neoplasm / immunology
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Chromosomes, Human, Pair 18 / genetics*
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Clinical Trials as Topic
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Epithelial-Mesenchymal Transition
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Female
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Gene Fusion
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Genetic Engineering
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Humans
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Immunotherapy, Adoptive / methods*
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Lymphocytes, Tumor-Infiltrating / physiology*
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Lymphocytes, Tumor-Infiltrating / transplantation
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Male
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Membrane Proteins / immunology
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Neoplasm Proteins / genetics
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Proto-Oncogene Proteins / genetics
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Receptors, Antigen, T-Cell / genetics*
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Recombinant Fusion Proteins / genetics*
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Repressor Proteins / genetics
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Sarcoma, Synovial / genetics
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Sarcoma, Synovial / immunology
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Sarcoma, Synovial / therapy*
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T-Lymphocytes / physiology*
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T-Lymphocytes / transplantation
Substances
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Antigens, Neoplasm
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CTAG1B protein, human
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Membrane Proteins
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Neoplasm Proteins
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Proto-Oncogene Proteins
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Receptors, Antigen, T-Cell
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Recombinant Fusion Proteins
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Repressor Proteins
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SS18 protein, human
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synovial sarcoma X breakpoint proteins