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ABSTRACT: Background
Data on the clinical features, optimal treatment and outcomes of paediatric patients with epithelioid sarcoma (ES) are limited and mostly retrospective.Methods
A subset analysis of ES patients < 30 years of age enrolled on two international prospective clinical trials conducted between 7/2005 and 11/2015 was performed. Risk-adapted therapy was based on tumour diameter, histologic grade, extent of surgery and presence/absence of metastases and included surgery ± radiotherapy for all patients with the addition of ifosfamide/doxorubicin chemotherapy for intermediate-/high-risk patients. Response to therapy, event-free and overall survival and pattern and predictors of treatment failure were evaluated.Results
Sixty-three ES patients (median age 13.1 years, 52
SUBMITTER: Spunt SL
PROVIDER: S-EPMC6944741 | biostudies-literature | 2019 May
REPOSITORIES: biostudies-literature