Stereotactic Body Radiotherapy (SBRT) for Spinal Tumors A Single Institution Experience

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J. Richelyn Baclay, MD

Abstract

Introduction:
Delivery of a single high dose or a few fractionated radiation treatments for spinal tumors through stereotactic body radiosurgery (SBRT) is now available in the Philippines. A retrospective review was performed to determine the rate of pain relief, toxicity, and neurologic outcomes of patients treated with this modality.


Methodology:
From 2012-2015, 24 patients were identified who underwent SBRT in this institution. Patients were selected for SBRT based on the RTOG 0631 eligibility checklist. Pain outcome was measured using the NRPS. Neurologic examination was done by the attending neurosurgeon. Acute effects were scored according to the CTC v3. Dose was determined by tumor histology, proximity to nearby structures, as well as computed tumor volume. The mean age of patients was 58 ± 16.06 years. Patients were treated to a median dose of 16Gy (range 12-25Gy), given in 1-5 fractions.


Results:
SBRT was performed in a total of 30 spinal tumors from 24 patients (7 primary, 23 metastatic). The most common tumor site was the thoracic spine. Pain was present in 18 of the patients pre-SBRT, with 83% documenting complete pain relief, one month after SBRT. Only one patient experienced pain flare which resolved with steroids, and one patient developed vertebral compression fracture two months after treatment. Of the 10 patients who had motor deficits pre-SBRT, 3 had complete recovery of motor function, while 7 had partial improvement.


Conclusions:
SBRT for spinal tumors is well-tolerated, safe, and effective treatment option. The results of our institution appear comparable to previous reports investigating outcomes of SBRT.

Article Details

How to Cite
BACLAY, J. Richelyn. Stereotactic Body Radiotherapy (SBRT) for Spinal Tumors. Philippine Radiation Oncology Society, [S.l.], sep. 2015. Available at: <https://research.pros.org.ph/index.php/pros/article/view/12>. Date accessed: 04 dec. 2024.
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