About this trial
The purpose of this study was to compare efficacy and side effects of two target delineation methods for stereotactic radiotherapy of metastatic spinal tumors.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients with spinal metastases or primary tumors receiving stereotactic radiotherapy;
Patients with sufficent pre-treatment imaging data
Patients who can cooperate with imaging review and follow-up after radiotherapy.
Disqualifiers
Patients with an expected survival of less than 3 months;
Patients with second-course radiotherapy;
Patients with physical conditions that cannot tolerate stereotactic radiotherapy;
Patients with extensive spinal metastasis and no local therapeutic value
Trial population
Patients with malignant tumor spinal metastasis who received or will receive stereotactic radiotherapy, without preoperation.
Trial design
Cohort
Other
Treatments tested in this trial
Target volume delineation
RadiationGroup 1(small target delineation):The target bolume only includes local tumor. Group 2(small target delineation):The target bolume includes local tumor and adjacent vertebral area.
Treatment groups
Trial outcomes
Primary outcomes
Disease Control Rate(DCR)
Disease Control Rate(DCR),including complete response(CR),partial response(PR) and stable disease(SD ).
Pain relief rate
VAS Score(Visual Analog Scale Score) decreased after treatment
Secondary outcomes
Incidence of side effects
radiation myelitis,radiation esophagitis, etc.
Sponsors and contacts
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