Clinical outcomes following stereotactic radiosurgery for brain metastases from sarcoma primaries: An international

Raj Singh1, John G Roubil2, Greg Bowden3

  • 1Department of Radiation Oncology, The James Cancer Hospital and Solove Research Institute, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.

Cancer
|June 21, 2025
PubMed
Abstract

Insights

Stereotactic radiosurgery (SRS) for brain metastases from sarcoma offers limited data. Leiomyosarcoma histology and younger age (<45) improved local control, while non-leiomyosarcoma histology and extracranial disease worsened overall survival.

Area of Science:

  • Neuro-oncology
  • Radiation Oncology
  • Sarcoma Research

Background:

  • Limited data exists on stereotactic radiosurgery (SRS) outcomes for brain metastases originating from sarcoma.
  • Sarcoma brain metastases represent a significant clinical challenge with few established treatment guidelines.

Purpose of the Study:

  • To evaluate treatment outcomes, including overall survival (OS) and local control (LC), following SRS for brain metastases from sarcoma.
  • To identify prognostic factors influencing survival and local control in this patient population.

Main Methods:

  • Retrospective analysis of 146 patients with sarcoma brain metastases treated with SRS across International Radiosurgery Research Foundation sites.
  • Kaplan-Meier analysis for OS and LC; univariate and multivariate Cox proportional hazards models to identify prognostic factors.

Main Results:

  • One- and 2-year OS rates were 47.7% and 37.3%, respectively; 1- and 2-year LC rates were 78.3% and 62.2%, respectively.
  • Leiomyosarcoma histology and age <45 years were associated with superior LC (HR, 0.31; P=.03 and HR, 3.78; P<.001, respectively).
  • Non-leiomyosarcoma histology (HR, 3.13; P=.006) and progressive extracranial metastases were associated with poorer OS.

Conclusions:

  • Local control after SRS for sarcoma brain metastases is influenced by histology and patient age.
  • Overall survival is significantly impacted by non-leiomyosarcoma histology and the presence of progressive extracranial disease.

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