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Treatment of Liver Metastases Using an Internal Target Volume Method for Stereotactic Body Radiotherapy
Published on: May 8, 2018
Treatment planning for in vivo multi-fraction, multi-port, multi-modal Synchrotron Radiotherapy.
Micah J Barnes1, Matthew Cameron2, Elette Engels3
1Centre of Medical Radiation Physics, University of Wollongong, Australia; Imaging and Medical Beamline, ANSTO Australian Synchrotron, Australia; Physical Sciences, Peter MacCallum Cancer Centre, Australia.
This study details microbeam radiotherapy (MRT) planning using the Eclipse treatment planning system (TPS) in mice, correlating dose with outcomes. Modified MRT schedules did not impact tumor control or metastasis, but reduced primary tumor volume.
Area of Science:
- Medical Physics
- Radiation Oncology
- Preclinical Cancer Research
Background:
- Treatment planning systems (TPSs) for microbeam radiotherapy (MRT) require enhancement for complex in-vivo studies.
- Existing literature lacks detailed dosimetry and planning data for linking MRT dose to treatment outcomes.
- This study addresses these gaps by detailing a synchrotron-based, fractionated MRT approach in tumor-bearing mice.
Purpose of the Study:
- To detail dosimetry, treatment planning, delivery, and evaluation for in-vivo microbeam radiotherapy (MRT) studies.
- To correlate physical dose with observed treatment outcomes in a preclinical model.
- To adapt and utilize the Eclipse TPS for fractionated, mixed-modality synchrotron radiotherapy.
Main Methods:
- Adapted the Eclipse TPS to accumulate dose for fractionated mixed-modality treatments.
- Employed manual plan optimization to meet dose prescriptions and constraints.
- Calculated and compared volumetric dose data for tumors, organs-at-risk, and metastases to treatment outcomes.
Main Results:
- Manual plan optimization met most requirements, limited by delivery system constraints.
- Dose accumulation for BB and MRT valleys was achieved; MRT peaks were assessed separately.
- Tumor control was maintained; primary tumor volume reduced by >32% with MRT, but metastases were not controlled. Temporal beam placement did not alter outcomes.
Conclusions:
- This work details the first use of Eclipse TPS for multi-fraction, multi-port, mixed-modality synchrotron radiotherapy.
- Provides crucial insights into treatment outcomes and biological endpoints relative to physical dose in MRT.
- Highlights the need for advanced TPS capabilities in preclinical MRT research.
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