NCT05155423Active, not recruitingNot Applicable
A Prospective Study of Performing MRI Simulation in Treatment Position in Spinal Stereotactic Body Radiation Therapy
M.D. Anderson Cancer Center2 sites in 1 country21 target enrollmentStarted: April 21, 2018Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- M.D. Anderson Cancer Center
- Enrollment
- 21
- Locations
- 2
- Primary Endpoint
- Performing MRI scans in the treatment position for accurate treatment planning.
Study Overview
Brief Summary
To learn the usefulness of performing MRI scans in different positions and learn the best practice for spinal stereotactic body radiation therapy (spinal SBRT) planning and dose delivery.
Detailed Description
1. Objectives
- Assess the feasibility of performing MRI scans in the treatment position for accurate treatment planning and dose delivery in spinal stereotactic body radiation therapy (spinal SBRT).
- Characterize the improved accuracy of image fusion between MRI and CT and its dosimetric impact when performing MRI scans in treatment position in spinal SBRT.
- Assess the ability of MRI simulation to accurately target extended spinal targets beyond the current targeting limitations (>3 consecutive vertebral body levels)
- Optimize the workflow of using MRI simulation in treatment planning and dose delivery.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Inclusion Criteria
- •Greater than or equal to 18 years of age
- •Pathologically confirmed diagnosis of cancer, including, but not limited to non-small cell lung cancer, breast, prostate, renal cell, melanoma, gastrointestinal, sarcoma, thyroid, head and neck primary, and carcinoma of unknown primary
- •Signed informed consent
- •Willing to undergo 2 MRI simulations in one or multiple sessions, one with immobilization device, and the other without.
- •Patients undergoing spinal SBRT 3.2.
Exclusion Criteria
- •a. Patient with a relative or absolute contraindication to MRI (such as pacemaker, etc.) b. Patients with significant instrumentation or cement at the site of interest causing artifact c. Inability to tolerate with immobilization device for greater than 30 minutes
Outcomes
Primary Outcomes
Performing MRI scans in the treatment position for accurate treatment planning.
Time Frame: through study completion, an average of 1 year
Performing MRI scans in the treatment position for dose delivery in spinal stereotactic body radiation therapy (spinal SBRT).
Time Frame: through study completion, an average of 1 year
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (2)
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