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A Mouse Model of Incompletely Resected Soft Tissue Sarcoma for Testing Neoadjuvant Therapies
Published on: July 28, 2020
Postoperative brain metastases in soft tissue sarcomas
Hiroshi Urakawa1, Satoshi Tsukushi, Eiji Kozawa
1Department of Orthopedic Surgery, Nagoya University Graduate School and School of Medicine, 65 Tsurumai, Showa-ku, Nagoya, Aichi, 466-8550, Japan, urakawa@med.nagoya-u.ac.jp.
Brain metastases are rare in soft tissue sarcoma (STS) but deadly. Neurofibromatosis-1 (NF-1), MPNST, and large tumors increase risk, necessitating vigilant brain metastasis surveillance for high-risk patients.
Area of Science:
- Oncology
- Surgical Oncology
- Neuro-oncology
Background:
- Brain metastases (BMs) from soft tissue sarcoma (STS) are infrequent but associated with poor prognosis.
- Identifying risk factors for BMs in STS is crucial for improving patient outcomes.
Purpose of the Study:
- To investigate the incidence and survival rates of BMs in STS patients.
- To identify factors associated with brain metastasis-free survival (BMFS) after surgery for STS.
Main Methods:
- Retrospective review of 187 STS patients treated with definitive surgery.
- Analysis of BMFS and overall survival (OS) after BM.
- Statistical investigation of factors influencing BMFS, including neurofibromatosis-1 (NF-1).
Main Results:
- Eight out of 187 STS patients (4.3%) developed BMs at a median of 18.2 months post-surgery.
- The 5-year BMFS rate was 95.2%, with a 3-month OS rate after BM of 25.0%.
- NF-1, malignant peripheral nerve sheath tumor (MPNST) histology, and primary tumor size ≥5 cm were significantly associated with increased BM incidence.
Conclusions:
- Postoperative BMs in STS are notably higher in patients with NF-1, MPNST, and large primary tumors.
- Careful surveillance for BMs is essential in NF-1 patients, particularly those with co-existing metastases.
- Early detection and management strategies are vital for improving survival in STS patients with BMs.
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