J Neurol Surg B Skull Base 2025; 86(S 01): S1-S576
DOI: 10.1055/s-0045-1803074
Presentation Abstracts
Podium Presentations
Oral Presentations

Hypofractionated Radiosurgery for Skull Base, Spinal, and Sacral Chordomas: A Systematic Review and Meta-analysis

Vinay Jaikumar
1   University at Buffalo Neurosurgery, Williamsville, New York, United States
,
Jaims Lim
1   University at Buffalo Neurosurgery, Williamsville, New York, United States
,
Seth Schrader
1   University at Buffalo Neurosurgery, Williamsville, New York, United States
,
Michael Liu
1   University at Buffalo Neurosurgery, Williamsville, New York, United States
,
Hanna N. Algattas
1   University at Buffalo Neurosurgery, Williamsville, New York, United States
,
Jason M. Davies
1   University at Buffalo Neurosurgery, Williamsville, New York, United States
,
Kenneth V. Snyder
1   University at Buffalo Neurosurgery, Williamsville, New York, United States
,
Adnan H. Siddiqui
1   University at Buffalo Neurosurgery, Williamsville, New York, United States
,
Elad I. Levy
1   University at Buffalo Neurosurgery, Williamsville, New York, United States
› Author Affiliations
 
 

    Introduction: Chordomas’ critical locations within skull base, spine, and sacrum limit the maximal dose that can be administered to ensure tumor regression. To mitigate radiation side-effects, fractionation protocols ensure the delivery of equivalent or higher total radiation in manageable fractions, while maintaining comparable side-effect profiles. Hypofractionated stereotactic radiosurgery (HF-SRS) is a fractionation strategy that administers higher doses per fraction (>2 Gy) necessitating fewer fractions overall, addressing potentially higher obliteration rates, low side-effects and ensuring patient compliance. We performed a systematic review and meta-analysis to evaluate the outcomes of HF-SRS utilization in the treatment of skull base, spinal and sacral chordomas and chondrosarcomas.

    Methods: PubMed and Embase were queried for literature on “hypofractionated” “radiosurgery” for “chordomas.” Data on patient and chordoma characteristics, procedural details, follow-up outcomes and survival were extracted from eligible studies. Meta-analyses using random-effects models were conducted on variables reported by ≥3 studies on R version 4.3.2.

    Results: We included 11 studies reporting 165 patients with a mean age of 47.69 years (43.38–52.43) (Tables 1 and 2), representing 58.04% (49.75–65.91) males. Skull base chordomas constituted 71.23% (57.61–81.86) with an additional 23.33% (15.72–33.17) detected in the mobile spine. Chondrosarcomas formed 12.49% (5.96–24.33) of all tumors. A mean dosage of 29.74 Gy (25.40–34.82) were delivered in 4.11 (3.59–4.71) fractions at 7.60 (7.18–8.04) Gy/fraction. On mean follow-up duration of 31.22 months (19.06–51.14), we observed 10.88% (5.89–19.21) radionecrosis and 11.28% (5.29–22.50) chordoma-related mortality rate. Overall survival was 92.64% (86.65–96.07), 89.91% (80.44–95.08), and 83.29% (67.24–92.37) at 1, 2, and 5 years, respectively, while progression-free survival respectively was 83.43% (74.36–89.73), 81.49% (72.50–88.03), and 72.47% (59.94–82.24).

    Conclusion: HF-SRS is promising among radiosurgical strategies for chordoma treatment with a low complication rate, indicating promise for potential first-line use. Significant heterogeneity in dosing regimens warrants additional investigation and necessitates homogenous reporting with the incorporation location specific chordoma, treatment and survival information.


    No conflict of interest has been declared by the author(s).

    Publication History

    Article published online:
    07 February 2025

    © 2025. Thieme. All rights reserved.

    Georg Thieme Verlag KG
    Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany