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Meningeal Solitary Fibrous Tumor: A Single-Center Retrospective Cohort Study

Authors :
Siyer Roohani
Yasemin Alberti
Maximilian Mirwald
Felix Ehret
Carmen Stromberger
Soleiman Fabris Roohani
Katja Bender
Anne Flörcken
Sven Märdian
Daniel Zips
David Kaul
Source :
Sarcoma, Vol 2024 (2024)
Publication Year :
2024
Publisher :
Hindawi Limited, 2024.

Abstract

Background. Meningeal solitary fibrous tumors (SFTs) are rare, malignant, mesenchymal tumors of the central nervous system. While surgical gross total resection is widely accepted as a positive prognostic factor for local control (LC), the role of postoperative radiotherapy (PORT) remains controversial. We sought to report our institutional experience with a particular focus on outcomes after PORT. Materials and Methods. In this single-center, retrospective cohort study, 20 patients with the primary diagnosis of histopathologically confirmed meningeal SFT were analyzed. Data on patient characteristics, imaging, treatment modalities, histopathology, and oncological outcomes were collected. LC and overall survival (OS) were assessed using the Kaplan–Meier estimator. Results. The median follow-up time was 95.8 months. After surgery only, 9 out of 11 patients (81.8%) developed a local recurrence while, after surgery and PORT, 3 out of 9 patients (33.33%) showed local failure. The 5- and 10-year LC rates were 50.5% and 40.4% in the surgery-only group and 80% at both time points in the surgery with the PORT group. In the surgery-only group, 4 out of 11 patients (36.4%) died, and 4 out of 9 patients (44.4%) died in the surgery and PORT group. OS rates after 5 and 10 years were 88.9% and 66.7% in the surgery-only group and 88.9% and 76.2% in the surgery with PORT group. Conclusions. Our findings suggest that PORT may improve LC in patients with meningeal SFT. The low incidence of meningeal SFT impedes prospective studies and requires further international collaborative efforts to exploit retrospective datasets and molecular analysis to improve patient outcomes.

Details

Language :
English
ISSN :
13691643
Volume :
2024
Database :
Directory of Open Access Journals
Journal :
Sarcoma
Publication Type :
Academic Journal
Accession number :
edsdoj.484252d4d30643e4bde17f44edb2b7f2
Document Type :
article
Full Text :
https://doi.org/10.1155/2024/8846018