Diagnosis and management of synovial sarcoma

被引:28
作者
Lor Randall R. [1 ]
Schabel K.L.S. [1 ]
Hitchcock Y. [1 ]
Joyner D.E. [1 ]
Albritton K.H. [1 ]
机构
[1] Sarcoma Services, Hunstman Cancer Institute, Salt Lake City, UT 84112
关键词
Sarcoma; Clin Oncol; Soft Tissue Sarcoma; Radiat Oncol Biol Phys; Synovial Sarcoma;
D O I
10.1007/s11864-005-0024-z
中图分类号
学科分类号
摘要
Synovial sarcoma is a unique tumor with substantial promise for biologically targeted therapy. Although it demonstrates moderate chemosensitivity, with approximately 50% response rates to ifosfamide- and doxorubicin-containing regimens, it has a diagnostic translocation and a potentially informative chimeric protein product. Although surgical management remains the cornerstone to effect local control, therapeutic advancements are unlikely to occur by continuing to include advanced cases of synovial sarcomas in trials with other soft tissue sarcomas. Rather, attention should be turned toward prospective molecular targets and development of novel agents to exploit them. Research should be directed at understanding the fusion protein of the X,18 translocation and further validating the role of overexpressed proteins in synovial sarcoma. Meanwhile, carefully designed clinical trials of these agents, with translational correlates, will provide in vivo data to complement the preclinical experience. Copyright © 2005 by Current Science Inc.
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页码:449 / 459
页数:10
相关论文
共 67 条
[1]  
Spurrell E.L., Fisher C., Thomas J.M., Judson I.R., Prognostic factors in advanced synovial sarcoma: An analysis of 104 patients treated at the Royal Marsden Hospital, Ann Oncol, 16, pp. 437-444, (2005)
[2]  
Mullen J.R., Zagars G.K., Synovial sarcoma outcome following conservation surgery and radiotherapy, Radiother Oncol, 33, pp. 23-30, (1994)
[3]  
Weiss S.W., Goldblum J.R., Malignant soft tissue tumors of uncertain type, Enzinger and Weiss's Soft Tissue Tumors, pp. 1485-1506, (2001)
[4]  
Pelmus M., Guillou L., Hostein I., Et al., Monophasic fibrous and poorly differentiated synovial sarcoma: Immunohistochemical reassessment of 60 t(X
[5]  
18)(SYT-SSX)-positive cases, Am J Surg Pathol, 26, pp. 1434-1440, (2002)
[6]  
Folpe A.L., Schmidt R.A., Chapman D., Gown A.M., Poorly differentiated synovial sarcoma: Immunohistochemical distinction from primitive neuroectodermal tumors and high-grade malignant peripheral nerve sheath tumors, Am J Surg Pathol, 22, pp. 673-682, (1998)
[7]  
Panagopoulos I., Mertens F., Isaksson M., Et al., Clinical impact of molecular and cytogenetic findings in synovial sarcoma, Genes Chromosomes Cancer, 31, pp. 362-372, (2001)
[8]  
Lopes J.M., Nesland J.M., Reis-Filho J.S., Holm R., Differential Ki67 and bcl-2 immunoexpression in solid-glandular and spindle cell components of biphasic synovial sarcoma: A double immunostaining assessment with cytokeratin and vimentin, Histopathology, 40, pp. 464-471, (2002)
[9]  
Antonescu C.R., Kawai A., Leung D.H., Et al., Strong association of SYT-SSX fusion type and morphologic epithelial differentiation in synovial sarcoma, Diagn Mol Pathol, 9, pp. 1-8, (2000)
[10]  
Llombart-Bosch A., Lopez-Guerrero J.A., Peydro-Olaya A., Synovial sarcoma (SS): New perspectives supported by modern technology, Arkh Patol, 64, pp. 39-47, (2002)