Local failure in childhood rhabdomyosarcoma and undifferentiated sarcoma: Prognostic factors and implications for curative therapy |
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Authors: | Hedy Mameghan,Richard Fisher,Vivienne Tobias,Ian B. Kern,Darcy O Gorman-Hughes,Marcus Vowels,Jill Mameghan |
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Affiliation: | Hedy Mameghan,Richard Fisher,Vivienne Tobias,Ian B. Kern,Darcy O′Gorman-Hughes,Marcus Vowels,Jill Mameghan |
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Abstract: | In this retrospective review, the risk factors for local failure in childhood rhabdomy-osarcoma and undifferentiated sarcoma were assessed in 49 patients managed by a multi-disciplinary team at the Prince of Wales Children′s Hospital, Sydney, between 1970 and 1988. Average follow-up time was 6.1 years. Sixteen of 49 patients experienced local failure defined as local recurrence after complete excision (5/20) or progressive local disease following incomplete resection (11/29). Fourteen of 16 patients who experienced local failure have died. Using logrank analysis of time to local failure, we found significantly increased risk with “non-embryonal” histology (P = 0.032), residual tumour (P = 0.052, higher IRS group (P = 0.088), “inadequate radiotherapy” for residual tumour (P = 0.001), delay in definitive local treatment (P = 0.038) and Adriamycin-containing chemotherapy (P = 0.017). When these factors were examined by multivariate analysis (Cox regression), only the presence of residual tumour after resection, “inadequate radiotherapy” for residual tumour (P < 0.001), and delay in definitive local therapy (P = 0.037) were shown to have independent significant association with local failure. We conclude that local failure may be avoided by prompt local treatment by either complete surgical resection or adequate radiotherapy. © 1993 Wiley-Liss, Inc. |
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Keywords: | rhabdomyosarcoma soft tissue sarcoma local failure survival |
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