Spine Stereotactic Body Radiation Therapy for Metastatic Epidural Spinal Cord Compression
Primary Purpose
Spinal Cord Compression
Status
Unknown status
Phase
Phase 2
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Stereotactic body radiation therapy
Sponsored by
About this trial
This is an interventional treatment trial for Spinal Cord Compression focused on measuring Stereotactic body radiation therapy, Radiosurgery
Eligibility Criteria
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)
Sites / Locations
- Samsung Medical CenterRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Stereotactic body radiation therapy
Arm Description
SBRT in one to four fractions Irradiated total RT dose to gross tumor volume (GTV) according to fraction size 1 fx: 16 to 24 Gy 2 fx's: 20 to 26 Gy 3 fx's: 21 to 30 Gy 4 fx's: 24 to 36 Gy
Outcomes
Primary Outcome Measures
Neurologic response
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.
Secondary Outcome Measures
Full Information
NCT ID
NCT01826058
First Posted
April 3, 2013
Last Updated
November 27, 2014
Sponsor
Samsung Medical Center
Collaborators
Seoul National University Hospital, Gachon University Gil Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT01826058
Brief Title
Spine Stereotactic Body Radiation Therapy for Metastatic Epidural Spinal Cord Compression
Official Title
Spine Stereotactic Body Radiation Therapy for Metastatic Epidural Spinal Cord: Prospective Phase II Study
Study Type
Interventional
2. Study Status
Record Verification Date
November 2014
Overall Recruitment Status
Unknown status
Study Start Date
October 2012 (undefined)
Primary Completion Date
June 2015 (Anticipated)
Study Completion Date
August 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Samsung Medical Center
Collaborators
Seoul National University Hospital, Gachon University Gil Medical Center
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Compression
Keywords
Stereotactic body radiation therapy, Radiosurgery
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
43 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Stereotactic body radiation therapy
Arm Type
Experimental
Arm Description
SBRT in one to four fractions
Irradiated total RT dose to gross tumor volume (GTV) according to fraction size
1 fx: 16 to 24 Gy
2 fx's: 20 to 26 Gy
3 fx's: 21 to 30 Gy
4 fx's: 24 to 36 Gy
Intervention Type
Radiation
Intervention Name(s)
Stereotactic body radiation therapy
Other Intervention Name(s)
Radiosurgery, SRS, Radiation, Radiotherapy, Metastatic Epidural Spinal Cord Compression, MESCC
Primary Outcome Measure Information:
Title
Neurologic response
Description
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.
Time Frame
1 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Doo Ho Choi, MD. PhD.
Phone
82-2-3410-2436
Email
doho.choi@samsung.com
First Name & Middle Initial & Last Name or Official Title & Degree
Donryul Oh, MD
Phone
82-2-3410-2613
Email
dongryuloh@gmail.com
Facility Information:
Facility Name
Samsung Medical Center
City
Seoul
ZIP/Postal Code
135-710
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Doo Ho Choi, MD.PhD.
Phone
82-2-3410-2436
Email
doho.choi@samsung.com
First Name & Middle Initial & Last Name & Degree
Dongryul Oh, MD
Phone
82-2-3410-2615
Email
dongryuloh@gmail.com
First Name & Middle Initial & Last Name & Degree
Doo Ho Choi, MD.PhD.
12. IPD Sharing Statement
Learn more about this trial
Spine Stereotactic Body Radiation Therapy for Metastatic Epidural Spinal Cord Compression
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