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Int. J. Radiat. Oncol. Biol. Phys. · Jun 2012
Optimizing normal tissue sparing in ion therapy using calculated isoeffective dose for ion selection.
- Nicholas B Remmes, Michael G Herman, and Jon J Kruse.
- Department of Radiation Oncology, Mayo Clinic, Rochester, MN 55905, USA.
- Int. J. Radiat. Oncol. Biol. Phys. 2012 Jun 1; 83 (2): 756-62.
PurposeTo investigate how the selection of ion type affects the calculated isoeffective dose to the surrounding normal tissue as a function of both normal tissue and target tissue α/β ratios.Methods And MaterialsA microdosimetric biologic dose model was incorporated into a Geant4 simulation of parallel opposed beams of protons, helium, lithium, beryllium, carbon, and neon ions. The beams were constructed to give a homogeneous isoeffective dose to a volume in the center of a water phantom for target tissues covering a range of cobalt equivalent α/β ratios of 1-20 Gy. Concomitant normal tissue isoeffective doses in the plateau of the ion beam were then compared for different ions across the range of normal tissue and target tissue radiosensitivities for a fixed isoeffective dose to the target tissue.ResultsThe ion type yielding the optimal normal tissue sparing was highly dependent on the α/β ratio of both the normal and the target tissue. For carbon ions, the calculated isoeffective dose to normal tissue at a 5-cm depth varied by almost a factor of 5, depending on the α/β ratios of the normal and target tissue. This ranges from a factor of 2 less than the isoeffective dose of a similar proton treatment to a factor of 2 greater.ConclusionsNo single ion is optimal for all treatment scenarios. The heavier ions are superior in cases in which the α/β ratio of the target tissue is low and the α/β ratio of normal tissue is high, and protons are superior in the opposite circumstances. Lithium and beryllium appear to offer dose advantages similar to carbon, with a considerably lower normal tissue dose when the α/β ratio in the target tissue is high and the α/β ratio in the normal tissue is low.Copyright © 2012 Elsevier Inc. All rights reserved.
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