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Journal of Clinical Oncology, 2005 ASCO Annual Meeting Proceedings.
Vol 23, No 16S (June 1 Supplement), 2005: 1582
© 2005 American Society of Clinical Oncology
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Abstract

Gliosarcoma - clinical study

P. S. Sridhar, R. Prabhakar, M. B. Pandey, D. N. Sharma, P. K. Julka and G. K. Rath

All India Institute Medcl Sciences (AIIMS), New Delhi, India

1582

Background: Gliosarcomas are rare neoplasm of central nervous system. Consisting gliomatous and sarcomatous components. No clear data is available regarding its cell of origin and behavior. This study examines clinical features, treatment and survival. Methods: 14 patients of Gliosarcomas treated between Jan 1993 to June 2004 were analyzed retrospectively.10 were male, 4 female, with median age of 50 years (range 12–70 yrs). All were situated in supratentorium, 8 were left side, 6 right side.7 in temporal region, 4 in temporoparietal and 3 in parietal region. All patients underwent surgery and 12 patients received postoperative radiotherapy to dose of 60 Gy/30 fractions in 6 weeks.10 patients received platinum based chemotherapy.2 patient received concurrent taxane and radiotherapy. Results: Median survival was 9.3 months, 10 patients died of disease, 2 patients stable disease, and 1 patient is in PR and 1 in CR. Conclusions: Gliosarcoma is aggressive neoplasm; Clinically indistinguishable from GBM.Chemoradiotherapy is beneficial

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Copyright © 2005 by the American Society of Clinical Oncology, Online ISSN: 1527-7755. Print ISSN: 0732-183X
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