医学
放射外科
危险系数
单变量分析
比例危险模型
多元分析
组织学
肉瘤
不利影响
内科学
肿瘤科
放射治疗
核医学
放射科
病理
置信区间
作者
Raj Singh,John G. Roubil,Greg Bowden,David Mathieu,Louise Carrier,Matthew J. Shepard,Trent Kite,Rodney E. Wegner,Piero Picozzi,Andrea Franzini,Huai‐Che Yang,Cheng‐Chia Lee,Zhishuo Wei,Andrew H. Hoang,Judith Hess,Bushra Fathima,Veronica Chiang,Selçuk Peker,Yavuz Samancı,Roman Liščák
出处
期刊:Cancer
[Wiley]
日期:2025-06-21
卷期号:131 (13)
摘要
Abstract Background There is a paucity of data on treatment outcomes following stereotactic radiosurgery (SRS) for brain metastases from sarcoma primaries. Methods The International Radiosurgery Research Foundation member‐sites were queried for patients with brain metastases from sarcoma primaries treated with SRS. Overall survival (OS) and local control (LC) were calculated via Kaplan–Meier analysis. Univariate analyses examined prognostic factors associated with LC and OS via log‐rank t ‐tests and multivariate analyses (MVA) via Cox proportional hazards model. Results A total of 146 patients with 309 brain metastases were identified. Two‐hundred and thirty lesions were treated with single‐fraction SRS with a median dose of 20 Gy (15–24 Gy). Ninety‐five patients had extracranial metastases, including 75 oligometastatic patients. One‐ and 2‐year OS and LC rates were 47.7% and 37.3%, and 78.3% and 62.2%, respectively. On univariate analyses, superior 1‐year OS was noted among leiomyosarcomas (69.7% vs. 42.6%; p = .02) with poorer outcomes among pleomorphic histologies (10.5% vs. 50.7%; p = .002). Pleomorphic histologies were associated with poorer OS on MVA (hazard ratio [HR], 3.13; p = .006). On MVA, LC was inferior among patients of age ≥45 years (HR, 3.78; p < .001) and superior among leiomyosarcomas (HR, 0.31; p = .03). OS was prognosticated based on adverse factors (ie, nonleiomyosarcoma histology and progressive extracranial metastases). Two‐year OS for patients with and without adverse features were 78.6% and 31.5%, respectively. Conclusions LC outcomes were driven by histology and age with superior LC among leiomyosarcomas and patients of age <45 years. OS was driven by nonleiomyosarcoma histology and the presence of progressive extracranial disease.
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