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Original Article
Myoid differentiation and prognosis in adult pleomorphic sarcomas of the extremity
An analysis of 92 cases
Article first published online: 16 JUL 2003
DOI: 10.1002/cncr.11617
Copyright © 2003 American Cancer Society
Additional Information
How to Cite
Deyrup, A. T., Haydon, R. C., Huo, D., Ishikawa, A., Peabody, T. D., He, T.-C. and Montag, A. G. (2003), Myoid differentiation and prognosis in adult pleomorphic sarcomas of the extremity. Cancer, 98: 805–813. doi: 10.1002/cncr.11617
Publication History
- Issue published online: 1 AUG 2003
- Article first published online: 16 JUL 2003
- Manuscript Accepted: 30 MAY 2003
- Manuscript Revised: 14 MAY 2003
- Manuscript Received: 26 FEB 2003
Funded by
- Brinson Foundation
- Orthopaedic Research and Education Foundation
- Abstract
- Article
- References
- Cited By
Keywords:
- myogenic;
- myoid;
- sarcoma;
- malignant fibrous histiocytoma (MFH);
- immunohistochemistry;
- prognosis
Abstract
BACKGROUND
The results of a recent study demonstrated an association between myoid differentiation and an adverse prognosis in adult patients with pleomorphic sarcoma, as determined by 5-year metastasis-free survival rates.
METHODS
To confirm the importance of muscle differentiation on prognosis in a well controlled clinical context, 92 samples from patients with pleomorphic sarcoma of the extremity from a single institution were immunostained with 4 monoclonal antibodies believed to be correlated with myoid differentiation: α-smooth muscle actin, muscle-specific actin, desmin, and myoglobin.
RESULTS
Forty-two cases were positive for at least 1 muscle marker and 50 cases were uniformly negative. Between the two groups, there was no significant difference in tumor size, tumor extent, or patient age found; however, histologic grade was significantly higher (P = 0.038) in the myoid tumors. The 5-year survival differed significantly between patients with myoid tumors (35%) and those without myoid tumors (65%) (P = 0.0054). Myoid differentiation remained an adverse prognostic indicator after adjusting for clinically significant factors (i.e., histologic grade, tumor size, tumor extent, and patient age) (P = 0.01) (hazard ratio, 2.39; 95% confidence interval, 1.24–4.63). Furthermore, there was an inverse relation found between the number of myoid markers present and survival (P = 0.004).
CONCLUSIONS
Myoid differentiation was found to be an independent indicator of adverse prognosis in adult patients with pleomorphic spindle cell sarcoma of the extremity. Cancer 2003;98:805–13. © 2003 American Cancer Society.
DOI 10.1002/cncr.11617

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