Palliative Lattice Stereotactic Body Radiotherapy (SBRT)
NCT04133415 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2021-11-22
Summary
Standard palliative radiotherapy regimens may provide limited durability of response in large tumors. Thus, there is a clinical need for a new approach. The Lattice SBRT approach will deliver 20 Gy in 5 fractions with partial volume simultaneous integrated boosts to 66.7 Gy. This is hypothesized to improve symptom response, local control, and better prime the tumor microenvironment for immune response compared with standard palliative radiotherapy doses. It is also hypothesized that this will be associated with less toxicity than the traditional homogenous SBRT plan delivered to a large tumor. Blood will be collected before and after Lattice SBRT for evaluation of the peripheral blood immune microenvironment.
Conditions
- Cancer
- Palliative Radiotherapy
Interventions
- RADIATION
-
Lattice stereotactic body radiation therapy
-As long as radiotherapy fields do not overlap, treatment of up to 4 other tumor sites are allowed
- PROCEDURE
-
Peripheral blood
-Before treatment, immediately after radiotherapy completion, 14 days after radiotherapy, and 30 days after radiotherapy
Sponsors & Collaborators
-
Washington University School of Medicine
lead OTHER
Principal Investigators
-
Matthew Spraker, M.D., Ph.D. · Washington University School of Medicine
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-10-31
- Primary Completion
- 2020-12-14
- Completion
- 2020-12-14
- FDA Device
- Yes
Countries
- United States
Study Locations
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