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Recruiting NCT06293157

Carbon Fiber Transpedicular Screws in Treatment of Spinal Metastatic Disease

No phase Interventional Metastatic Spinal Cord Compression Metastasis Spine

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Transpedicular spinal stabilization - carbon fibers-based implants, Transpedicular spinal stabilization - titanium implants, Stereotactic body radiotherapy.
Who it may be relevant to
Registry conditions: Metastatic Spinal Cord Compression, Metastasis Spine. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Poland
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Carbon Fiber Transpedicular Screws in Treatment of Spinal Metastatic Disease and Stereotactic Radiotherapy - a Prospective, Randomized Trial

Overview

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.

Interventions

  • Procedure Transpedicular spinal stabilization - carbon fibers-based implants
    Transpedicular stabilization with carbon fiber and PEEK-based implants in one of the two possible variants - first involves a large skin incision and separation of the back extensor muscles; second is associated with minimally invasive, which is percutaneous procedure that allows the stabilization with implants without the need to detach the muscles, using only a small skin incision.
  • Procedure Transpedicular spinal stabilization - titanium implants
    Transpedicular stabilization with titanium implants in one of the two possible variants - first involves a large skin incision and separation of the back extensor muscles; second is associated with minimally invasive, which is percutaneous procedure that allows the stabilization with implants without the need to detach the muscles, using only a small skin incision.
  • Radiation Stereotactic body radiotherapy
    Spinal tumors will be treated with stereotactic body radiotherapy at a dose of 5x5 Gy (25 Gy in a total dose); either prior to or post-surgical treatment, accordingly the allocation to one of the study arms.

Primary outcome measures

  • The assessment of time to local recurrence after treatment with SBRT. [Time frame: 5 years]
  • The assessment of frequency of local recurrence after treatment with SBRT. [Time frame: 5 years]
Secondary outcome measures (11)
  • DICE convergence factor evaluation between groups of patients. [Time frame: 1 day]
  • The subjective difficulty of planning radiotherapy treatment. [Time frame: 1 day]
  • The frequency of radiation complications assessed according to the National Cancer Institute Common Toxicity Criteria (NCI CTC). [Time frame: 5 years]
  • Failure rate of stabilizing systems. [Time frame: 5 years]
  • Pain assessment on the VAS scale between groups. [Time frame: 5 years]
  • Frequency of postoperative infections. [Time frame: 5 years]
  • Differences in dosimetric parameter Dmin PTV/CTV. [Time frame: 1 day]
  • Differences in dosimetric parameter D95. [Time frame: 1 day]
  • Differences in dosimetric parameter D98. [Time frame: 1 day]
  • Differences in dosimetric parameter D100. [Time frame: 1 day]
  • Differences in dosimetric parameter conformity index (CI) / homogeneity index (HI)). [Time frame: 1 day]

Eligibility criteria

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Poland · 5 centers
  • Department of Neurosurgery, Functional Neurosurgery and Stereotaxy, Dr. Jan Biziel Univers — Bydgoszcz
  • Professor Franciszek Łukaszczyk Oncology Center in Bydgoszcz - National Research Institute — Bydgoszcz
  • Department of Teleradiotherapy, Lower Silesian Center of Oncology, Pulmonology and Hematol — Wroclaw
  • University Center of Neurology and Neurosurgery, Jan Mikulicz-Radecki University Clinical — Wroclaw
  • Copernicus Memorial Hospital in Łódź, Poland — Lodz

Publications

  • Cofano F, Di Perna G, Monticelli M, Marengo N, Ajello M, Mammi M, Vercelli G, Petrone S, Tartara F, Zenga F, Lanotte M, Garbossa D. Carbon fiber reinforced vs titanium implants for fixation in spinal metastases: A comparative clinical study about safety and effectiveness of the new "carbon-strategy". J Clin Neurosci. 2020 May;75:106-111. doi: 10.1016/j.jocn.2020.03.013. Epub 2020 Mar 12. PMID 32173153
  • Boriani S, Tedesco G, Ming L, Ghermandi R, Amichetti M, Fossati P, Krengli M, Mavilla L, Gasbarrini A. Carbon-fiber-reinforced PEEK fixation system in the treatment of spine tumors: a preliminary report. Eur Spine J. 2018 Apr;27(4):874-881. doi: 10.1007/s00586-017-5258-5. Epub 2017 Aug 16. PMID 28815357
  • Nevelsky A, Borzov E, Daniel S, Bar-Deroma R. Perturbation effects of the carbon fiber-PEEK screws on radiotherapy dose distribution. J Appl Clin Med Phys. 2017 Mar;18(2):62-68. doi: 10.1002/acm2.12046. Epub 2017 Feb 7. PMID 28300369
  • Ringel F, Ryang YM, Kirschke JS, Muller BS, Wilkens JJ, Brodard J, Combs SE, Meyer B. Radiolucent Carbon Fiber-Reinforced Pedicle Screws for Treatment of Spinal Tumors: Advantages for Radiation Planning and Follow-Up Imaging. World Neurosurg. 2017 Sep;105:294-301. doi: 10.1016/j.wneu.2017.04.091. Epub 2017 May 3. PMID 28478252
  • Neal MT, Richards AE, Curley KL, Patel NP, Ashman JB, Vora SA, Kalani MA. Carbon fiber-reinforced PEEK instrumentation in the spinal oncology population: a retrospective series demonstrating technique, feasibility, and clinical outcomes. Neurosurg Focus. 2021 May;50(5):E13. doi: 10.3171/2021.2.FOCUS20995. PMID 33932921
  • Lindtner RA, Schmid R, Nydegger T, Konschake M, Schmoelz W. Pedicle screw anchorage of carbon fiber-reinforced PEEK screws under cyclic loading. Eur Spine J. 2018 Aug;27(8):1775-1784. doi: 10.1007/s00586-018-5538-8. Epub 2018 Mar 1. PMID 29497852
  • Krystkiewicz K, Kuncman L, Orzechowska MJ, Pytlarz B, Kowal A, Siwak M, Fijuth J, Ranoszek K, Pajdzinski M, Zubiel K, Arczewski F, Dziedzic K, Tosik M. CARBOMETASPINE: protocol for a multicenter, prospective, randomized controlled trial of carbonfiber spinal fixation in metastatic disease. BMC Cancer. 2025 Sep 2;25(1):1409. doi: 10.1186/s12885-025-14731-7. PMID 40898139

Identifiers

NCT: NCT06293157 · 2023/ABM/01/00013

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗