University Medical Center Utrecht
Utrecht, 3584 CX, Netherlands
NCT Number: NCT02622841
The aim of this study is to assess the feasibility and safety of combining stereotactic body radiotherapy (SBRT) and pedicle screw fixation in a 48-hour window for the treatment of painful unstable metastases of the thoracic and/or lumbar spine.
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Notify Me18 year and older
All sexes
Interventional
Phase 1 / Phase 2
Utrecht, 3584 CX, Netherlands
Rationale: Sixty-five percent of cancer patients with terminal illness have bone metastases, with debilitating pain as devastating consequence. The spine is the most common location for bone metastases. Spinal cord compression is present in 10% of patients with vertebral metastases and aggravates pain and performance status even further. Standard treatment of unstable vertebral metastases consists of stabilizing surgery, followed by external beam radiotherapy (8 Gy) after two weeks. Although this approach is effective in 60-70% of patients, it is has several downsides. Firstly, because of the two weeks interval between surgery and external beam radiotherapy, necessary for sufficient wound healing, it takes a long time before radiotherapy induced pain relief is achieved. Scatter artifacts on planning computed tomography images caused by surgical implants prohibit high-resolution imaging and accurate targeting of the lesion. Multiple hospital visits (+/- 10) are needed for administration of external beam irradiation, and in about 30-40% of patients no adequate pain response is achieved. An alternative treatment strategy, which would lead to faster pain relief in a higher proportion of patients with less hospital visits, would be highly desirable from the patient's perspective.
Objective: To assess the feasibility and safety of combining stereotactic body radiotherapy (SBRT) and pedicle screw fixation in a 48-hour window for the treatment of painful unstable metastases of the thoracic and/or lumbar spine.
Study design: Prospective case series (13), first in man study, Phase I and II a study according to the IDEAL recommendations
Study population: All patients, male and female, with impending spinal stability requiring radiation therapy and surgical intervention at the University Medical Center Utrecht
Main study parameters/endpoints: The main outcome of this study is safety of the combined procedure, defined as grade 3 or higher treatment-induced toxicity according to common terminology criteria for adverse events (CTC-AE) 4.0 as a result of the procedure within 60 days after the surgery.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Stereotactic bodyradiotherapy and surgical stabilization within 48 hours.
Time frame: first 90 days post treatment
Occurrence of adverse events grade 3/4 according to the common terminology criteria for adverse events (CTCAE) 4.0
Time frame: first 90 days post treatment
Measurement of pain response to combined therapy according to consensus guidelines
Time frame: first 90 days post treatment
Measurement of duration of pain relief
Time frame: first 90 days post treatment
Measurement of rapidity of pain relief
Time frame: first 90 days post treatment
Measurement of length of hospital stay
Time frame: First 30 days post treatment
Measurement of 30 days mortality
Time frame: First 90 days post treatment
Measurement of neurological deterioration
Time frame: first 90 days post treatment
Evaluation of quality of life
Time frame: Time from inclusion until date of death from any cause assessed up to 100 months
Overall survival
UMC Utrecht
Other
Stereotactic Body Radiotherapy Followed by Surgical Stabilization for Patients With Unstable Spinal Metastases: First-in-Man Study According to the IDEAL Recommendations
Acronym: BLEND
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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