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Objective@#To use TLDs and radiochromic films to verify the prescribed doses to both planned target volume (PTV) and organ at risk (OAR) and the 2D dose distribution in IMRT.@*Methods@#Eight accelerators of different models were selected in Henan province. The polystyrene phantom provided by IAEA was scanned using CT scanners and then the scanned images were transmitted to treatment planning system (TPS) for prescribing respectively the doses to PTV and OAR. IMRT was performed with phantom exposed to a 6 MV X-rays. The irradiated TLDs and films were delivered for measurement and estimation at Secondary Standard Dosimetry Laboratory at National Institute for Radiological Protection, Chinese Center for Disease Control and Prevention.@*Results@#According to IAEA requirements, the relative deviations of the TLD-measured and TPS-planned values were within ±7.0% for the prescribed doses to PTV and OAR. The measured results for PTV have shown that the relative deviation of TLD-measured and TPS-planned values were within -0.3% to 6.9% for 8 accelerators, all consistent with the IAEA requirements. For OAR, the relative deviations of TLD-measured and TPS-planned were within -7.0% to 0.3% for 6 accelerators, consistent with the requirements, whereas those for other 2 accelerators were within -10.8% to -8.4%, not up to the requirements. IAEA required that, for 2D dose distribution, the pass rate of 3 mm/3% be ≥90%. The measured values for 7 accelerators were from 90.2% to 99.9%, consistent with the requirements, whereas that for another one was 70.0%, not meeting the requirement.@*Conclusions@#The method to verify, using radiochromic film and TLD, the prescribed doses to PTV and OAR and the pass rate of 2D dose distribution is simple and reliable. It is an important step to implement quality control for IMRT and can provide effective support for medical or third-party service institution to verify clinically prescribed dose.
ABSTRACT
Objective To use TLDs and radiochromic films to verify the prescribed doses to both planned target volume (PTV) and organ at risk (OAR) and the 2D dose distribution in IMRT.Methods Eight accelerators of different models were selected in Henan province.The polystyrene phantom provided by IAEA was scanned using CT scanners and then the scanned images were transmitted to treatment planning system (TPS) for prescribing respectively the doses to PTV and OAR.IMRT was performed with phantom exposed to a 6 MV X-rays.The irradiated TLDs and films were delivered for measurement and estimation at Secondary Standard Dosimetry Laboratory at National Institute for Radiological Protection,Chinese Center for Disease Control and Prevention.Results According to IAEA requirements,the relative deviations of the TLD-measured and TPS-planned values were within ±7.0％ for the prescribed doses to PTV and OAR.The measured results for PTV have shown that the relative deviation of TLD-measured and TPS-planned values were within-0.3％ to 6.9％ for 8 accelerators,all consistent with the IAEA requirements.For OAR,the relative deviations of TLD-measured and TPS-planned were within-7.0％ to 0.3％ for 6 accelerators,consistent with the requirements,whereas those for other 2 accelerators were within-10.8％ to-8.4％,not up to the requirements.IAEA required that,for 2D dose distribution,the pass rate of 3 mm/3％ be ≥ 90％.The measured values for 7 accelerators were from 90.2％ to 99.9％,consistent with the requirements,whereas that for another one was 70.0％,not meeting the requirement.Conclusions The method to verify,using radiochromic film and TLD,the prescribed doses to PTV and OAR and the pass rate of 2D dose distribution is simple and reliable.It is an important step to implement quality control for IMRT and can provide effective support for medical or third-party service institution to verify clinically prescribed dose.
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Objective To validate the absorbed dose and two-dimensional dose distribution from photon beam by using Thermoluminescent dosimeter (TLD) and film for intensity modulated radiation therapy (IMRT).Methods A total of 8 medical accelerators were selected among 5 third-grade first-class hospitals using non-probabilistic sampling method in Henan province.TLDs were put into polytetrafluoroethylene solid phantom with size of 5 cm × 15 cm × 15 cm provided by IAEA.After CT scanning,the radiotherapeutic plans were formulated through image transmission to the treatment planning system (TPS).The IMRT plan was implemented for measurement of TLD-absorbed doses under the conditions of 5 cm × 5 cm field,90 cm SSD,10 cm depth,6 MV photon beam and 6 Gy absorbed dose and corresponding measurement unit (MU).The 25 cm × 25 cm film-absorbed dose measurement was made in the same manner as TLD under the conditions of 30 cm × 30 cm size,20 cm thickness,95 cm SSD and 5 cm depth.Results Of eight accelerators,the requirements can be met for 7 accelerators with respect to the relative deviation of TLD absorbed dose except 1.For film,relative deviations were all consistent with the requirements.The passing rate of two-dimensional dose distribution was in line with the requirements for 7 accelerators except 1.Conclusions TLD and film can be used to check the MLC field absorbed dose and two-dimensional dose distribution.This methodis simple,easy to operate and suitable for the implementation of IMRT quality control in hospitals in Henan province.
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Objective To verify the reliability of radiotherapy dosimetric parameters in reference and non-reference conditions using thermoluminescent dosimeters (TLDs).Methods Using the established TLD method,the dose variations with different radiation field sizes and 45 ° wedge plate were verified for 10 photon beams of 6 MV,together with dosimetric parameters at the point of maximum axial dose for 4 electron beams of 9 MeV under reference and non-reference conditions.Comparisons were made between TLD results and finger ionization chamber results.Results The average relative deviation,for 6 MV photon beams,between TLD results and finger ionization chamber measurements was 4.7％,within ± 7％ as required by the IAEA.The average relative deviation,for 9 MeV electron beam,between TLD results and plane parallel ionization chamber measurements was 2.4 ％,not beyond ± 5％ permitted by IAEA.Conclusions Using TLD method to verify the radiotherapy dosimetric parameters in reference and non-reference conditions was reliable,simple and feasible.
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In order to analyze the image noise effect on the results of Gamma knife dosimetry parameter test, we tested the dosimetry parameters of the Gamma knives according to GBZ 168-2005. Radiological protection standards of X (gamma)-ray stereotactic radiosurgery for head treatment. Dose analysis software was applied to examine the testing film before and after image denoising, and SPSS 11.0 software was used for statistical analysis. The results showed that there was a significant difference in the results of the maximum deviation between radiation field size and its nominal value (t = 7.600, P < 0.01) and the radiation field's penumbra region width of collimators also had significantly different sizes (t = 5.334, P < 0.01) before and after image denoising. This study indicated that the image noise could influence the results of testing Gamma knife dosimetry parameters, so as to cause deviations.