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Spine Stereotactic Body Radiation Therapy for Metastatic Epidural Spinal Cord Compression

Spine Stereotactic Body Radiation Therapy for Metastatic Epidural Spinal Cord: Prospective Phase II Study

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01826058
Enrollment
43
Registered
2013-04-08
Start date
2012-10-31
Completion date
2015-08-31
Last updated
2014-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Cord Compression

Keywords

Stereotactic body radiation therapy, Radiosurgery

Brief summary

Metastatic epidural spinal cord compression (MESCC) is a frequent oncologic emergency that requires to be treated promptly. Although direct decompressive surgery is the most effective treatment, surgery is only used in selected patients because most patients have a poor overall condition and short life expectancy. Radiation therapy (RT), therefore, is the most commonly used for patients with MESCC, but conventional RT alone can achieve modest neurologic outcomes. The hypothesis to use stereotactic body radiation therapy (SBRT) for MESCC is that the rapid decompression of epidural mass, durable local control and subsequently improved neurologic outcomes compared to conventional RT are expected when MESCC is treated with SBRT.

Detailed description

The definition of metastatic epidural spinal cord compression (MESCC) * MESCC is defined as both an evidence of cord compression by radiologic evaluation and a manifestation of clinical feature at the level of cord compression. * A cord compression by radiologic evaluation is defined as \< 3mm gap between epidural mass and true spinal cord or indentation of thecal sac at the level of clinical feature by MRI. * Clinical features include any or all of the followings: pain (local or radicular) or motor weakness or sensory change or incontinence. Simulation -A Computed tomography (CT) scan will be acquired with the use of intravenous contrast and planning MRI will be also performed on the same day of simulation. Spine SBRT \- One to four sessions of SBRT will be performed. Follow-up * Patients need to be assessed at 1 week, 1 month and 3 months after the completion of SBRT and will be followed up at 3 month intervals thereafter. * Pain score, neurologic examination, adverse events and simple X-ray of involved spine should be evaluated at every follow-up visit. * MRI of involved spine will be performed at 3 months after the completion of SBRT. Up to 43 patients will be enrolled in this study in Samsung Medical Center, Seoul National University Hospital, and Gachon University Gil Medical Center.

Interventions

RADIATIONStereotactic body radiation therapy

Sponsors

Seoul National University Hospital
CollaboratorOTHER
Gachon University Gil Medical Center
CollaboratorOTHER
Samsung Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* MESCC is present. * Localized spine metastases (C1 to L5 level); Maximum 3 separate sites and maximum 2 contiguous vertebral bodies * Performance state before the occurrence of neurologic symptoms : Eastern Cooperative Oncology Group 0-2 * Age ≥20 * MRI within 2 weeks is mandatory * Paraspinal mass \< 5cm in maximum dimension * Inoperable patients - refused or medically unfit for decompression surgery * life expectancy \> 3 months

Exclusion criteria

* Retropulsed bony fragment causing cord compression * Paraplegia ≥ 48 hours * Histology preferred to perform the chemotherapy as the first option (e.g. lymphoma, myeloma)

Design outcomes

Primary

MeasureTime frameDescription
Neurologic response1 month* Neurologic response is defined as maintaining grade 4 or more motor power after completing SBRT or as an increase of motor power by at least 1 grade from the baseline motor power. * There should no decrease of motor power after completing SBRT. * The motor weakness is graded from 0 to 5 by Medical Research Council (MRC) scale.

Countries

South Korea

Contacts

Primary ContactDoo Ho Choi, MD. PhD.
doho.choi@samsung.com82-2-3410-2436
Backup ContactDonryul Oh, MD
dongryuloh@gmail.com82-2-3410-2613

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026