Demonstrate the technical feasibility of treating spine metastases with image-guided radiosurgery/SBRT
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
1
•24 Gy in 3 fractions to cover at least 90% of the defined target volume
16 Gy in 1 fraction to cover at least 90% of the defined target volume
Department of Clinical Oncology, Prince of Wales Hospital
Hong Kong, Hong Kong
Pain control at 3 months post-treatment
Time frame: 4 years
Determine the time of onset of pain response of the responders at the treated site(s) using radiosurgery/SBRT
Time frame: 4 years
Determine the duration of pain response at the treated site(s) using radiosurgery/SBRT
Time frame: 4 years
Study the adverse events of radiosurgery/SBRT according to the criteria in the CTEP Active Version of the CTCAE
Time frame: 4 years
Evaluate the radiological response of image-guided radiosurgery/SBRT by RECIST MRI
Time frame: 4 years
2-year Tumor Control Rate
Time frame: 4 years
Overall Survival
Time frame: 4 years
Quality of life assessment
Time frame: 4 years
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