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Vertebral Compression Fracture After Spine Stereotactic Body Radiotherapy: The Role of Vertebral Endplate Disruption
Khaled Dibs1, Benjin Facer1, Prasath Mageswaran2
1Department of Radiation Oncology, The James Cancer Hospital at the Ohio State University Wexner Medical Center, Columbus , Ohio , USA.
Neurosurgery
|October 30, 2023
Summary
Endplate disruption is a new risk factor for vertebral compression fractures (VCF) after spinal stereotactic body radiotherapy (SBRT). A nomogram combining endplate disruption, adverse histology, and Spinal Instability Neoplastic Score (SINS) effectively stratifies VCF risk.
Area of Science:
- Radiation Oncology
- Spinal Surgery
- Radiology
Background:
- Vertebral compression fracture (VCF) is a serious toxicity of spinal stereotactic body radiotherapy (SBRT).
- Advanced Spinal Instability Neoplastic Score (SINS) is a known risk factor for VCF.
- The role of tumoral endplate (EP) disruption in VCF risk is not well understood.
Purpose of the Study:
- To investigate the association between tumoral endplate (EP) disruption and the risk of VCF after spinal SBRT.
- To develop a risk stratification system for VCF incorporating EP disruption.
Main Methods:
- Retrospective cohort study of 111 patients undergoing spinal SBRT (2013-2019).
- Pre-SBRT CT scans assessed for EP disruption.
- 1-year cumulative incidence of VCF assessed via follow-up MRI and CT scans.
Main Results:
- 43% of patients had at least one EP disruption.
- 18% of patients experienced VCF within 1 year.
- Patients with EP disruption had a significantly higher VCF risk (29% vs. 6%, P < .001).
- A nomogram incorporating EP disruption, SINS (≥7), and adverse histology stratified patients into low (2% VCF risk) and high (38% VCF risk) groups (P < .001).
Conclusions:
- Tumoral endplate (EP) disruption is a novel and significant risk factor for VCF following spinal SBRT.
- A simple nomogram including EP disruption, adverse histology, and SINS score aids in rapid VCF risk assessment.
- Further prospective studies are needed to validate these findings and inform patient counseling and prophylactic interventions.

