Soft‐tissue sarcomas (STS) are rare tumors that account for 1% of all adult malignancies,
with over 100 different histologic subtypes occurring predominately in the trunk, extremity …

Soft tissue sarcomas (STS) are rare solid tumors of mesenchymal cell origin that display a
heterogenous mix of clinical and pathologic characteristics. STS can develop from fat …

Purpose This guideline provides evidence-based recommendations addressing the
indications for radiation therapy (RT), sequencing of local therapies, and appropriate dose …

Leiomyosarcoma (LMS) is a soft tissue sarcoma of smooth muscle origin that can arise in
multiple anatomical sites and is broadly classified as extra-uterine LMS or uterine LMS …

Purpose: In a single-institution phase II study, we evaluated the safety of a 5-day dose-
equivalent neoadjuvant radiotherapy (RT) regimen for high-risk primary soft tissue sarcoma …

Simple Summary Myxofibrosarcomas (MFS) are malignant soft tissue tumors, frequently
located in the extremities. Owing to the infiltrative growth pattern of MFS, neoadjuvant …

Simple Summary Soft tissue sarcomas of the extremities are rare tumors with various
prognostic factors. The gold standard curative treatment relies on surgery with negative …

Introduction In extremity soft tissue sarcoma (ESTS), external beam radiotherapy (EBRT) has
been used in addition to limb-sparing surgery (LSS). This study aims to identify predictors for …

Background Previous studies have demonstrated an association of perioperative
radiotherapy (RT) with improved survival in patients with synovial sarcoma (SS) undergoing …

Small randomized trials have not shown an overall survival (OS) difference among local
treatment modalities for patients with extremity soft‐tissue sarcomas (E‐STS) but were …