SU-E-T-602: Dynamic Electron Arc Radiotherapy (DEAR): A Planning Study.

Conference Paper

PURPOSE: Electron beam therapy is under-utilized in radiation treatment of cancer and has remained practically unchanged for decades. We propose a new technique, Dynamic Electron Arc Radiotherapy (DEAR) with synchronized couch motion. In DEAR, gantry rotation, dose rate, and intensities are modulated to create desirable dose distributions free of hot and/or cold spots, with high homogeneity, and narrow penumbra. This study demonstrates the potential of DEAR in improving dose distributions. METHODS: Dose distributions for single-field and two-field were compared to DEAR with equal and optimized beam weights on a 32 cm diameter cylindrical phantom. Plans were designed to irradiate equivalent field size on the phantom surface, with the target dimension extending from 315° -45° in radial angle and target depth at 1 cm (6 MeV) or 2 cm (9 MeV). Penumbra (20-80%), dose homogeneity, and dose area histogram (DAH) were evaluated at target depths. Plans were calculated with the eMC algorithm in Eclipse v10. RESULTS: In-plane (longitudinal direction) penumbra was comparable across all plans as expected. Cross-plane (along curved surface) penumbra was 5.0, 1.5, and 2.0 cm (6 MeV) and 5.6, 1.7, and 2.1 (9 MeV), for single-field, two-field, and DEAR, respectively. While the two-field penumbra was better, it exhibited a hot spot 60% higher than the target mean at the beam junction covering approximately 20% of the target. DEAR plans displayed homogenous dose distributions with variations of less than ±1.5%. DAH of the single-field failed to achieve optimal coverage, while the two-field displayed a high-dose tail (>100%). 90% of the target receives at least 95% (two-field) and 88% (DEAR) of the target dose. CONCLUSION: Preliminary findings show that DEAR can produce homogenous dose distributions over large and curved targets without hot and/or cold spots while maintaining narrow penumbra. Future work includes planning for various target shapes and desired dose distributions.

Full Text

Duke Authors

Cited Authors

  • Rodrigues, A; Yin, F; Wu, Q

Published Date

  • June 2013

Published In

Volume / Issue

  • 40 / 6Part20

Start / End Page

  • 344 -

PubMed ID

  • 28519099

Electronic International Standard Serial Number (EISSN)

  • 2473-4209

Digital Object Identifier (DOI)

  • 10.1118/1.4815030

Conference Location

  • United States