Abstract
Background: Soft tissue sarcomas (STS) are a heterogeneous group of mesenchymal malignancies that occur throughout the lifespan. The impact of age on disease features and outcome is unclear. Methods: We analyzed the clinical features and outcome of all STS cases registered between 1973 and 2006 in the SEER database. Results: There were 48,012 cases that met the selection criteria. Individuals less than 20 years of age represented 5.6%, with rhabdomyosarcoma being the most common subtype. In adults, the most common types were Kaposi sarcoma, fibrohistiocytic tumors, and leiomyosarcoma. Rhabdomyosarcoma was the only entity with a median age
Original language | English |
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Pages (from-to) | 943-949 |
Number of pages | 7 |
Journal | Pediatric Blood and Cancer |
Volume | 57 |
Issue number | 6 |
DOIs | |
Publication status | Published - Dec 1 2011 |
Keywords
- Age
- Epidemiology
- Prognosis
- SEER
- Soft tissue sarcoma
ASJC Scopus subject areas
- Oncology
- Pediatrics, Perinatology, and Child Health
- Hematology