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Trial Title:
A Single-center Observational Clinical Trial of Stereotactic Radiotherapy on Metastatic Spinal Tumors Using TomoTherapy
NCT ID:
NCT05808998
Condition:
Spinal Bone Metastases
Radiation Therapy
Conditions: Official terms:
Neoplasm Metastasis
Study type:
Observational
Overall status:
Not yet recruiting
Study design:
Time perspective:
Prospective
Intervention:
Intervention type:
Radiation
Intervention name:
Stereotactic body radiotherapy
Description:
Stereotactic body radiotherapy using TomoTherapy
Summary:
A single-center observational clinical trial will be performed for metastatic spinal
tumors by stereotactic radiotherapy using TomoTherapy. In this study, we will explore the
local control rate (LCR), disease-free progression time (PFS), overall survival time
(OS), and pain relief in patients with spinal metastasis, so as to provide a basis for
developing relevant guidelines or consensus.
Detailed description:
In this observational single-arm study, a total of 45 patients with metastatic spinal
tumors will be enrolled. The patients were aged between 18 and 75 years old. And all the
subjects should meet the inclusion criteria and sign the informed consent. Meanwhile, the
patients' medical history characteristics, including gender, age, imaging data (X-ray,
CT, MRI, or PET-CT, etc.), primary tumor type, pathological type, previous treatment,
previous disease history, tumor markers and bone metabolism indexes were collected and
recorded on the CRF. The metastatic spinal tumors by stereotactic radiotherapy(SBRT)
using TomoTherapy. The adiotherapy dose is 6Gy×5Fx, 5Gy×5Fx or 4Gy×5Fx according to the
irradiation site. Treatment should be interrupted if there is severe bone marrow
suppression, vertebral compression fracture, or radiation myelitis. The adjacentnormal
tissue constrains refer to the UK SABR Consortium Guidelines (2022 version). Follow-up
was performed 1 month after radiotherapy, thereafter every 3 months for 1-4 years. The
parameters includ blood routine, liver and kidney function, bleeding and coagulation
function, bone metabolism index, tumor markers, bone metastasis imaging examination.
Tumor response will refer to the Cancer Response Criteria and Bone Metastases: RECIST
1.1, MDA and PERCIST.
Criteria for eligibility:
Study pop:
A total of 45 patients with spinal metastases were enrolled in this study.
Sampling method:
Probability Sample
Criteria:
Inclusion Criteria:
1. Spinal metastasis diagnosed by emission computed tomography, X-ray examination,
computed tomography, magnetic resonance imaging (MRI) or 18F-fluorodeoxy glucose
positron emission tomography within 6 weeks before enrollment;
2. Patients with unresectable spinal metastases;
3. SBRT was for patients with painful spinal metastases, physiological hypofunction,
decreased behavioral capacity and quality of life. And SBRT was used to help to
prevent or delay skeletal related event (SRE). Including postoperative radiotherapy
(especially post-separation), single or salvage radiotherapy;
4. age 18-75 years old;
5. KPS score equal to 70 points or over;
6. Patients were required to have histologically confirmed metastatic disease from
solid tumors, such as breast cancer, renal carcinoma or liver cancer;
7. The distance between metastatic lesion and spinal cord was more than 3mm；
8. Hemoglobin >90g/L, white cells count≥3.5×109/L, platelet count≥80×109/L, within 1
week before treatment;
9. No birth plans for the duration of study participation and up to 3 months following
completion of therapy;
10. Sign the informed consent.
Exclusion Criteria:
1. Spinal cord or cauda equina compression, the rapid decrement of neurological
function or paralysis;
2. A compression fracture of the spine, spinal instability and subsequent inability to
lie on back;
3. Metastatic lesions more than 5cm;
4. Multilevel segments involvement, including more than 5 metastatic segments, or 3
isolated lesions, or exceed two adjacent vertebrae;
5. The treatment site had received prior radiotherapy prior to the initiation of the
study;
6. Complicated with other malignant tumors or severe internal diseases affected the
prognosis;
7. Cannot tolerate radiation therapy, including the ones with scleroderma or connective
tissue diseases, or cann't complete the radiation treatment according to the
research;
8. Pregnant women or breast feeding mothers;
9. Systemic radionuclide therapy within 30 days before SBRT, or external radiotherapy
within 90 days before SBRT;
10. Pathologically confirmed as myeloma or lymphoma.
Gender:
All
Minimum age:
18 Years
Maximum age:
75 Years
Healthy volunteers:
No
Start date:
April 1, 2023
Completion date:
April 1, 2025
Lead sponsor:
Agency:
Shanghai Zhongshan Hospital
Agency class:
Other
Source:
Shanghai Zhongshan Hospital
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05808998
