Abstract:e23539 Background: Synovial sarcoma (SS) is a rare, high-grade soft tissue tumor and often requires multidisciplinary care with different treatment modalities. However, information on treatment patterns, especially in patients with localized disease and impact on survival is currently lacking. Methods: Adolescents and young adults (AYA, 15-39 years) and older adults (“adults,” ≥40 years) diagnosed with localized SS from 2000-2018 were identified in the California Cancer Registry. Treatment for SS consists of … Show more
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