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Pilot Study of Same-session MR-only Simulation and Treatment With Stereotactic MRI-guided Adaptive Radiotherapy (SMART) for Oligometastases of the Spine

Not Applicable
Completed
Conditions
Oligometastases of the Spine
Interventions
Device: MRIdian Linac System from ViewRay
Radiation: Stereotactic MRI-guided Adaptive Radiotherapy
Registration Number
NCT03878485
Lead Sponsor
Washington University School of Medicine
Brief Summary

In light of the increasing experience with magnetic resonance image-guided radiotherapy (MRgRT) and adaptive planning and advances in magnetic resonance (MR)-only planning, the investigators propose here to evaluate the feasibility and safety of same-session MR-only simulation and treatment with SMART for spinal metastases. Although spine SBRT is a standard-of-care treatment modality, this expedited same-session MR-only simulation and treatment with SMART workflow is novel. Previously, delivery of spine SBRT has typically required several days from time of consultation to simulation and then 1-2 weeks from simulation to the initiation of treatment. On this proposed study, patients will not undergo computed tomography (CT) simulation and will instead have same-session MR-only simulation and treatment planning, on-table, using SMART. In this manner, patients would initiate treatment within just several days from the consult. Feasibility of the workflow will be defined as successful delivery of the first fraction of same-session MRI-only simulation and treatment with SMART on the first on-table attempt for at least 70% of patients. Patients will be treated in five fractions over 1-2 weeks. Although the long-term goal will be to achieve a significantly shortened time from consult to treatment as compared to traditional stereotactic body radiation therapy (SBRT) using simulation, the present study will be driven by short-term goals of workflow feasibility and safety.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
10
Inclusion Criteria
  • At least one disease site deemed to be suitable for treatment with spine SBRT as per radiation oncology evaluation.
  • Karnofsky Performance Status (KPS) ≥ 60.
  • Deemed medically fit for SBRT by treating physician
  • Diagnostic CT with images through the projected treatment area within six months prior to enrollment.
  • At least 18 years of age.
  • Ability to understand and willingness to sign an IRB approved written informed
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Exclusion Criteria
  • Past history of radiotherapy within the projected treatment field to be treated by MRI-guided SBRT
  • Medical contraindication to undergoing MR imaging.
  • Spine metastasis resulting in symptomatic spinal cord compression.
  • Any other condition that, in the opinion of the treating radiation oncologist, renders the patient unfit for SBRT.
  • Pregnant and/or breastfeeding. Women of childbearing potential must have a negative pregnancy test within 14 days of study entry.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Stereotactic MRI-guided Adaptive RadiotherapyMRIdian Linac System from ViewRay-Radiotherapy will consist of stereotactic body therapy to the spine, to be given over either a two or five fraction course, delivered once daily or once every other day for a period of one to two weeks, for a total of two or five treatments (depending on whether a 2 or 5 fraction course is selected).
Stereotactic MRI-guided Adaptive RadiotherapyStereotactic MRI-guided Adaptive Radiotherapy-Radiotherapy will consist of stereotactic body therapy to the spine, to be given over either a two or five fraction course, delivered once daily or once every other day for a period of one to two weeks, for a total of two or five treatments (depending on whether a 2 or 5 fraction course is selected).
Primary Outcome Measures
NameTimeMethod
Number of Participants to Receive Delivery of the First Fraction of Same-session MRI-only Simulation and Treatment With SMART on the First On-table AttemptFirst on-table attempt of first fraction of radiation (an average of 1 day)
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Washington University School of Medicine

🇺🇸

Saint Louis, Missouri, United States

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