Carbon Fiber Transpedicular Screws in Treatment of Spinal Metastatic Disease and Stereotactic Radiotherapy - a Prospective, Randomized Trial
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 226
- 试验地点
- 6
- 主要终点
- The assessment of time to local recurrence after treatment with SBRT.
研究概览
简要总结
Background: Spinal metastatic disease constitute a serious clinical problem in oncology. Bones are the third most common organ where metastases are located, and the spine is the place where they are most often located. Due to the complexity of the clinical problem, metastatic spine disease remains of interest to many medical specialties: neurosurgery, orthopedics, clinical oncology, radiotherapy and rehabilitation. With the development of modern diagnostic methods and wider access to them, the demand for neurosurgical treatment in this group of patients is growing. Surgical treatment is undertaken in cases of spinal cord compression, instability, spinal deformation or pain that is resistant to radiotherapy. The standard treatment in most cases is posterior instrumentation of the spine using titanium pedicle screws. Unfortunately, these systems cause numerous artifacts in diagnostic imaging, both in CT and MRI. These distortions make it difficult to plan radiotherapy and determine the optimal dose that would avoid healthy tissues. Moreover, artifacts could make difficult postoperative follow-ups aimed at assessing local recurrence. The solution to these problems is the use of radiolucent implants. There are systems based on carbon fibers embedded in PEEK which do not cause typical artifacts for titanium implants.
Study plan: The open, three-arm, prospective randomized study is planned to involve 226 patients with metastatic disease of the spine, with a known or undiagnosed primary site. Patients will be qualified for 2 types of interventions. The first one includes treatment with stereotactic radiotherapy (SBRT) in the first stage of treatment and early instrumentation of the spine with titanium implants. The second type of intervention includes patients qualified for surgical treatment using spine stabilization and postoperative SBRT. Patients within this arm will be randomized into two groups differing in the type of material the instrumentation is made of: carbon-PEEK or titanium. The study group will be patients stabilized with carbon implants, and the control group will be those who will have titanium implants.
Study population: The study includes adult patients with metastatic spine disease, with a known or unknown primary tumor, qualified for SBRT and surgical treatment.
Assumed effects: It is assumed that the treatment proposed in the project would extend progression free survival by several months or achieve local control in an additional 5% of patients. Moreover, by improving the quality of imaging, earlier diagnosis of local recurrences and implementation of appropriate locoregional treatment would be possible.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Metastatic spinal disease,
- •ECOG quality of life of 0-2,
- •Eligibility for SBRT treatment,
- •Expected survival time >3 months,
- •Signed informed consent to participate in the study,
- •Sufficient organ capacity allowing to survive the perioperative period.
排除标准
- •Primary tumor of the spine,
- •Age <18 years old,
- •Expected survival time <3 months,
- •Eligibility for palliative radiotherapy,
- •No informed consent to participate in the study,
- •Pregnancy or breastfeeding,
- •The advancement of the disease preventing the technical use of implants.
结局指标
主要结局
The assessment of time to local recurrence after treatment with SBRT.
时间窗: 5 years
The assessment of frequency of local recurrence after treatment with SBRT.
时间窗: 5 years
次要结局
- Differences in dosimetric parameter D95.(1 day)
- The frequency of radiation complications assessed according to the National Cancer Institute Common Toxicity Criteria (NCI CTC).(5 years)
- Failure rate of stabilizing systems.(5 years)
- Frequency of postoperative infections.(5 years)
- Differences in dosimetric parameter conformity index (CI) / homogeneity index (HI)).(1 day)
- DICE convergence factor evaluation between groups of patients.(1 day)
- The subjective difficulty of planning radiotherapy treatment.(1 day)
- Pain assessment on the VAS scale between groups.(5 years)
- Differences in dosimetric parameter Dmin PTV/CTV.(1 day)
- Differences in dosimetric parameter D98.(1 day)
- Differences in dosimetric parameter D100.(1 day)
研究者
Kamil Krystkiewicz
Principal Investigator
Copernicus Memorial Hospital
