Abstract
BackgroundThe application of spacer gel represents a promising approach to reliably spare the rectal frontal wall during particle therapy (IJROBP 76:1251-1258, 2010). In order to qualify the spacer gel for the clinical use in particle therapy, a variety of measurements were performed in order to ensure the biological compatibility of the gel, its physical stability during and after the irradiation, and a proper definition of the gel in terms of the Hounsfield Unit (HU) values for the treatment planning system. The potential for the use of the spacer gel for particle therapy monitoring with off-line Positron Emission Tomography (PET) was also investigated.ResultsThe spacer gel implanted to the prostate patient in direct neighbourhood to the clinical target volume does not interfere with the particle therapy treatment planning procedure applied at Heidelberg Ion Beam Therapy Centre (HIT). The performed measurements show that Bragg-peak position of the particles can be properly predicted on the basis of computed tomography imaging with the treatment planning system used at HIT (measured water equivalent path length of 1.011 ±0.011 (2σ), measured Hounsfield Unit of 28.9 ±6.1 (2σ)). The spacer gel samples remain physically unchanged after irradiation with a dose exceeding the therapeutic dose level. The independently measured Bragg-Peak position does not change within the time interval of 10 weeks.ConclusionsAs a result of the presented experiments, the first clinical application of spacer gel implant during prostate cancer treatment with carbon ions and protons was possible at HIT in 2012. The reported pre-clinical investigations demonstrate that use of spacer gel is safe in particle therapy in presence of therapy target motion and patient positioning induced particle range variations. The spacer gel injected between prostate and rectum enlarge the distance between both organs, which is expected to clinically significantly decrease the undesirable exposure of the most critical organ at risk, i.e. rectal frontal wall. Further research on the composition of spacer gel material might lead to additional clinical benefits by validation of particle therapy of prostate via post-therapeutic PET-imaging or by patient positioning based on the gel as a radio-opaque marker.
Highlights
The application of spacer gel represents a promising approach to reliably spare the rectal frontal wall during particle therapy (IJROBP 76:1251-1258, 2010)
The results of the reference measurements obtained in measurement session 1, 2 and 3 were normalised on the basis of the range measurement performed without any absorber to calculated value
As the variation of the Bragg-Peak position for the spacer gel and for water is of the same magnitude within all three measurement sessions, one can conclude that no relevant changes in the range of carbon ions in the gel were observed within 10 weeks period
Summary
The application of spacer gel represents a promising approach to reliably spare the rectal frontal wall during particle therapy (IJROBP 76:1251-1258, 2010). For pre-treatment patient positioning the Heidelberg Ion Beam Therapy Centre, Heidelberg, Germany (HIT) offers image guided radiation therapy based on a digital X-ray system This implies the application of a bony anatomy registration protocol for the positioning of prostate cancer patients. The tendency to apply a hypofractionated prostate treatment protocol emphasises this problem [9,10] For these reasons the application of soft tissue like spacer gel (SpaceOARTMSystem, Augmenix Inc., Waltham, MA, US) enlarging the distance between radiotherapy target and organ at risk [11], not inducing particle range variations, represents a promising approach to reliably spare the rectal frontal wall during particle therapy. At HIT first prostate patients were treated with scanned carbon ion and proton beams using spacer gel in early 2012
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